FIELD OF THE INVENTION

[1] Embodiments of the present disclosure relate to medical apparatus, and more particularlyto,a system and a method for vaginal assessment.

BACKGROUND

[2] The number of women suffering from cervical cancer has been exponentially increasing. Post radiation, women suffer from dry vaginal passage and after a few months post radiation, adhesions begin to form in woman’s vaginal passage. The formation of adhesions takes place due to lack of oxygen supply to vaginal tissues. In addition to forming adhesions, the vaginal passage starts to shrink, and vaginal muscles weaken and gradually lose their tone.

[3] In order to overcome the aforementioned issues, the devices currently available only provide a tube as a vaginaldilator and a lubricant is required to use the tube, wherein the tube is made of hard rubber layers or latex. The available vaginal dilator material causes severe injuries in the vaginal passage.

[4] In furtherance to the aforementioned issue, a medical practitioner assisting a patient with the vaginal dilator is unable to understand the positions of the formed adhesions and the rigidness of the formed adhesions in order to help the patient get rid of the adhesions.

[5] Further, the medical practitioner may find it difficult to keep a track of numerous patients’ conditions, such as, rigidness of the adhesions and stages of stiffness of the vaginal passage.

[6] Therefore, there is a requirement a system that can overcome the aforementioned issues.

BRIEF DESCRIPTION

[7] In accordance with one embodiment of the disclosure, a method for vaginal assessment is provided. The method includes receiving, by an input module, a first sensed data from a first set of sensors provided in the vaginal exerciser, wherein the first sensed data comprises a first amount of external force applied by the vaginal exerciser to a corresponding adhesion formed in a vaginal passage. [8] The method also includes receiving, by the input module, a second sensed data from a second set of sensors provided in the vaginal exerciser, wherein the second sensed data comprises a second amount of force applied by contraction of a plurality of muscles of vaginal passage to the vaginal exerciser.

[9] The method also includes analysing, by a training module, at least one of the first sensed data and the second sensed data received from the input module based on a corresponding threshold data, wherein the corresponding threshold data comprises one or more forces applied by the external force and the contraction of the one or more vaginal muscles. The method also includesbuilding, by the training module, a personalised support model for vaginal exercise based on analysed data.

[10] The method also includes discharging, by a liquid discharging unit, via an actuator, liquid corresponding to the personalised support model for the vaginal exercise.

[11] In accordance with one embodiment of the disclosure, a system for vaginal assessment is disclosed. The system includes an interface unit, wherein the interface unit includes an input module. The input module is configured to receive a first sensed data from a first set of sensors provided in the vaginal exerciser, wherein the first sensed data includes a first amount of external force applied, by the vaginal exerciser, to a corresponding adhesion formed in a vaginal passage.

[12] The input module is also configured to receive a second sensed data from a second set of sensors provided in the vaginal exerciser, wherein the second sensed data includes a second amount of force applied by contraction of a plurality of muscles of the vaginal passage to the vaginal exerciser.

[13] The interface unit also includes a training module configured to analyse at least one of the first sensed data and the second sensed data received from the input module based on a corresponding threshold data, wherein the corresponding threshold data includes one or more forces applied by the external force and the contraction of the one or more vaginal muscles. The training module is also configured to build a personalised support model for vaginal exercise based on analysed data.

[14] The interface unit also includes a liquid discharging unit configured to discharge, via an actuator, liquid corresponding to the personalised support model for the vaginal exercise. [15] In an aspect, the present disclosure provides a method (30) for vaginal assessment, comprising:

receiving, by an input module (1002), a first sensed data from a first set of sensors (1016) provided in the vaginal exerciser, wherein the first sensed data comprises a first amount of external force applied by the vaginal exerciser to a corresponding adhesion formed in a vaginal passage;

receiving, by the input module (1002), a second sensed data from a second set of sensors (1018) provided in the vaginal exerciser, wherein the second sensed data comprises a second amount of force applied by contraction of a plurality of muscles of vaginal passage to the vaginal exerciser;

analysing, by a training module (1004), at least one of the first sensed data and the second sensed data received from the input module (1002) based on a corresponding threshold data, wherein the corresponding threshold data comprises one or more forces applied by the external force and the contraction of the one or more vaginal muscles;

building, by the training module (1004), a personalised support model for vaginal exercise based on analysed data; and

discharging, by a liquid discharging unit (1006), via an actuator, liquid corresponding to the personalised support model for the vaginal exercise.

[16] In another aspect, the analysing by the training module (1004) further comprises, identifying depth of the vaginal passage based on a chromatic material reacting to one or more secretions produced in the vaginal passage comprised in the vaginal exerciser.

[17] In another aspect, the analysing by the training module (1004), at least one of the first sensed data and the second sensed data received from the input module (1002), further comprises tracking, by a tracking module (1020), progress achieved by a user, wherein tracking progress achieved by the user is based on at least one of reduction in liquid from the liquid discharging unit (1006), reduction in one or more adhesions.

[18] In another aspect, the analysing by the training module (1004), at least one of the first sensed data and the second sensed data received from the input module (1002), further comprises notifying, by a notification module (1022), at least one of tracked data and the analysed data to at least one of the user and a medical practitioner. [19] In another aspect, the analysing, by the training module, further comprises analysing strength of a plurality of external vaginal muscles based on at least one vibrating level received from vaginal exerciser via the input module.

[20] In an aspect, the present disclosure provides a system (10) for vaginal assessment, comprising:

an interface unit (1000), operatively coupled to a vaginal exerciser, wherein the interface unit (1000) comprises:

an input module (1002) configured to:

receive a first sensed data from a first set of sensors (1016)provided in the vaginal exerciser, wherein the first sensed data comprises a first amount of external force applied, by the vaginal exerciser, to a corresponding adhesion formed in a vaginal passage;

receive a second sensed data from a second set of sensors (1018) provided in the vaginal exerciser, wherein the second sensed data comprises a second amount of force applied by contraction of a plurality of muscles of the vaginal passage to the vaginal exerciser;

a training module (1004) configured to:

analyse at least one of the first sensed data and the second sensed data received from the input module (1002) based on a corresponding threshold data, wherein the corresponding threshold data comprises one or more forces applied by the external force and the contraction of the one or more vaginal muscles;

build a personalised support model for vaginal exercise based on analysed data; and

a liquid discharging unit (1006) configured to discharge, via an actuator, liquid corresponding to the personalised support model for the vaginal exercise.

[21] In another aspect, the first set of sensors (1016)and the second set of sensors (1018) comprises a pressure sensor.

[22] In another aspect, the liquid discharging unit (1006) is configured to discharge the liquid, wherein the liquid discharging unit (1006) is operatively coupled to the vaginal exerciser, wherein the liquid comprises pH-level detector, anaesthetic, an anti-fungal composition and a lubricant.

[23] In another aspect, the training module is further configured to analyse strength of a plurality of external vaginal muscles based on at least one vibrating level received from vaginal exerciser via the input module. [24] In another aspect, the training module (1004) further comprises a tracking module (1020) configured to track progress achieved by a user, wherein the progress achieved by the user is based on at least one of the first sensed data, the second sensed data, the revised first and second threshold, respectively, reduction in liquid, reduction in one or more adhesions, achieved toned plurality of internal and external vaginal muscles.

[25] In another aspect, the training module (1004) further comprises a notification module (1022) configured to notify at least one of tracked data and the analysed data to at least one of the user and a medical practitioner.

[26] To further clarify the advantages and features of the present disclosure, a more particular description of the disclosure will follow by reference to specific embodiments thereof, which are illustrated in the appended figures. It is to be appreciated that these figures depict only typical embodiments of the disclosure and are therefore not to be considered limiting in scope. The disclosure will be described and explained with additional specificity and detail with the appended figures.

BRIEF DESCRIPTION OF THE DRAWINGS

The disclosure will be described and explained with additional specificity and detail with the accompanying figures in which:

[27] FIG. 1 illustrates a block diagram of a system for vaginal assessment in accordance with an embodiment of the present disclosure;

[28] FIG. 2illustrates an exemplary embodiment of the system for vaginal assessment in accordance with an embodiment of the present disclosure;

[29] FIG. 3 illustrates a block level diagram the system for vaginal assessment in accordance with an embodiment of the present disclosure; and

[30] FIG. 4illustrates a flow chart representing steps involved in a method for vaginal assessment in accordance with an embodiment of the present disclosure.

[31] Further, those skilled in the art will appreciate that elements in the figures are illustrated for simplicity and may not have necessarily been drawn to scale. Furthermore, in terms of the construction of the device, one or more components of the device may have been represented in the figures by conventional symbols, and the figures may show only those specific details that are pertinent to understanding the embodiments of the present disclosure so as not to obscure the figures with details that will be readily apparent to those skilled in the art having the benefit of the description herein.

DETAILED DESCRIPTION

[32] For the purpose of promoting an understanding of the principles of the disclosure, reference will now be made to the embodiment illustrated in the figures and specific language will be used to describe them. It will nevertheless be understood that no limitation of the scope of the disclosure is thereby intended. Such alterations and further modifications in the illustrated system, and such further applications of the principles of the disclosure as would normally occur to those skilled in the art are to be construed as being within the scope of the present disclosure.

[33] The terms "comprises", "comprising", or any other variations thereof, are intended to cover a non-exclusive inclusion, such that a process or method that comprises a list of steps does not include only those steps but may include other steps not expressly listed or inherent to such a process or method. Similarly, one or more devices or sub- systems or elements or structures or components preceded by "comprises... a" does not, without more constraints, preclude the existence of other devices, sub-systems, elements, structures, components, additional devices, additional sub-systems, additional elements, additional structures or additional components. Appearances of the phrase "in an embodiment", "in another embodiment" and similar language throughout this specification may, but not necessarily do, all refer to the same embodiment.

[34] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by those skilled in the art to which this disclosure belongs. The system, methods, and examples provided herein are only illustrative and not intended to be limiting.

[35] In the following specification and the claims, reference will be made to a number of terms, which shall be defined to have the following meanings. The singular forms“a”,“an”, and“the” include plural references unless the context clearly dictates otherwise.

[36] FIG. 1 illustrates a block diagram of a system (10) for vaginal assessment in accordance with an embodiment of the present disclosure. The system (10) includes an interface unit (1000), wherein the interface unit (1000) is operatively coupled to a vaginal exerciser.

[37] The vaginal exerciser includes a first part (100), second part (200), a third part (300) and a support unit (600), wherein the first part (100) is operatively coupled to the second part (200) and the third part (300). In one embodiment, the second part (200) may be operatively coupled to the third part (300). The first part (100) includes a first set of sensors, a first set of openings (1008) and a first closable orifice (112).

[38] In one embodiment, the first part (100), the second part (200) and the third part (300) of the vaginal exerciser are fabricated of, including but not limited to, silicone and chromatic material, wherein in one embodiment, the silicone may be of medical graded silicone. The first part (100) includes a calibration means to measure length of a vaginal passage. In one embodiment, the calibration means may be a scale in centimeters.

[39] The first part (lOO)is configured to break one or more adhesions formed in a vaginal passage. The first part (lOO)may be curved and hollow in nature to provide ease of movement into the vaginal passage. In one embodiment, the vaginal exerciser may be a phallus shaped. The first closable orifice (112) is configured to enable filling of liquid into the first part (100). The liquid includes a plurality of pH-level indicators, an anti-fungal composition, a lubricant and an anaesthetic. The liquid when discharged out of the first set of openings (1008) and the second set of openings (1010), provides localized anaesthetic effect and eases the entry of the vaginal exerciser into the vaginal passage without causing any frictions, thereby breaking the one or more adhesions.

[40] The pH-level indicators are, including but not limited to, a micro colouring agent which have colour changing characteristic when exposed to the vaginal secretions which have specific pH-level. The micro colouring agents are also sensitive for acidic levels in blood, which gets secreted from vaginal passage while breakage of the one or more adhesions. When the micro colouring agents comes in a contact with these secretions, the micro colouring agents change their colour, thereby coating the outer surface of the vaginal exerciser, which in turn displays the exact vaginal passage dilated area to the user. As the liquid includes a plurality of pH-level indicators, the plurality of secretions is noted based on the pH-level of corresponding secretions. [41] The second part (200) includes a second set of sensors (1018) (not shown in figures), a second set of openings (1010) and a second closable orifice (208). The second part (200) may be hollow and cylindrical in nature. The second closable orifice (208) is configured to enable filling of the liquid into the second part (200). The second part (200) is configured to strengthen a plurality of internal vaginal muscles. The second part (200) includes a calibration means to measure length of a vaginal passage. In one embodiment, the calibration means may be a scale in centimetres.

[42] The third part (300) includes a plurality of vibrators (1012) and an internal support unit (not shown in figures). The third part (300) is configured to strengthen a plurality of external vaginal muscles. The plurality of vibrators (1012) is figured to strengthen the plurality of external vaginal muscles. In one embodiment, the internal support unit may be configured to be received into the vaginal passage of a patient, wherein the internal support unit may be curved, or phallus shaped in nature. In another embodiment, the internal handle may be configured to be coupled to the first part (100), wherein the first part (100) may act as a support in holding up the third part (300) against the plurality of external vaginal muscles when inserted into the vaginal passage. In one embodiment, the plurality of vibrators (1012) may be replaced with a plurality of simulators.

[43] The interface unit (1000) includes an input module (1002), a training module (1004) and a liquid discharge unit (1006). The interface unit (1000) may be, including but not limited to, a phone, a television and a laptop.

[44] When the first part (100) of the vaginal exerciser is being inserted into the vaginal passage of the patient, the first part (100) upon coming in contact with the one or more adhesions, the first set of sensors (1016)are configured to sense a first amount of force applied to the one or more adhesions formed in the vaginal passage applied by a user via the first part (100) of the vaginal exerciser. The user may be, including but not limited to, the patient and a medical practitioner.

[45] The input module (1002) is configured to receive first sensed data from the first set of sensors (1016)provided in the first part (100), wherein the first sensed data represents the first amount of force. The first amount of force is applied in a first linear direction by the user to a corresponding one or more adhesions formed in the vaginal passage. In one embodiment, the first linear direction may be representative of a horizontal direction in which the first part (100) of the vaginal exercisers being inserted into the vaginal passage of the patient by the medical practitioner or the patient.

[46] The first sensed data is stored in a database (1014, FIG. 2). The first sensed data is also provided to the training module (1004), wherein the training module (1004) receives the first sensed data. A first threshold level is set bythe medical practitioner corresponding to the patient, wherein the first threshold level set for a corresponding patient is stored in the database (1014).

[47] Based on the first amount of force encountered by the first set of sensors, the training module (1004) enables the liquid discharging unit (1006)to discharge a corresponding first amount of liquid into the vaginal passage via the first set of openings (1008), wherein the training module (1004) is operatively coupled to the liquid discharging unit (1006).

[48] In one embodiment, the liquid discharging unit (1006) may include, but not limited to, a plunger rod (not shown in figures) with a plunger tip (not shown in figures) and an actuator (not shown in figure), wherein the plunger rod is operatively coupled with the actuator, wherein in one embodiment, the actuator may bea motor (not shown in figures). The plunger rod is configured to pass through the vaginal exerciser, wherein the plunger rod is enabled to move to and fro in the vaginal exerciser. However, the movement of the plunger tip is limited within the first part (100) of the vaginal exerciser.

[49] The training module (1004) signals the motor to push the plunger rod forward corresponding to the first sensed data, wherein the plunger rod is configured to push corresponding amount of the liquid into the vaginal passage via the first set of openings (1008).

[50] For example, say there are ten levels of the first amount of force that could be applied to the one or more adhesions. If a second level of force is applied to the one or more adhesions, then the training module (1004) enables the liquid discharging unit (1006)to discharge an amount of liquid, into the vaginal passage, corresponding to the second level of force applied to the one or more adhesions. Similarly, if a sixth level or a tenth level of force is applied to the one or more adhesions, then the training module (1004) enables the liquid discharging unit (1006)to discharge an amount of liquid, into the vaginal passage, corresponding to the sixth level or the tenth level of force applied to the one or more adhesions. The first amount of force applied, and the corresponding amount of liquid discharged are stored in the database (1014). Therefore, for each patient, different levels of force, that is the threshold levels, to be applied to the one or more adhesions formed in corresponding patients is stored in the database (1014), thereby building a personalised support module for each patient. In one embodiment, if the user, say the medical practitioner applies an amount of force greater than a first threshold value for a patient, the training module (1004)compares the additional amount of force applied by the medical practitioner to the one or more adhesions formed in the vaginal passage with the first threshold value. The value of additional amount of force is stored in the database (1014), thereby revising the first threshold value in the personalised support model built for a respective patient. Depending on the revised threshold value of the amount of force to be applied to the one or more adhesions, a new corresponding amount of liquid is pushed into the vaginal passage by the liquid discharging unit (1006) via the first set of openings (1008). Therefore, new value of the new corresponding amount of liquid to be discharged is also stored in the database (1014).

[51] In one embodiment, the training module signals the liquid discharging unit (1006) to push the corresponding liquid into the vaginal passage after calculating the amount of the liquid available in the first part (100). If the amount of liquid in the first part is less than a threshold level, then the training module alerts the user.

[52] In another embodiment, if the user, say the medical practitioner applies an amount of force greater than the first threshold value for a patient, the training module (1004) enables the medical practitioner to override the first threshold value, thereby storing the revised threshold value for the patient and revising the personalised support model for the patient. Depending on the new threshold value of the amount of force to be applied to the one or more adhesions, a new corresponding amount of liquid is discharged by the liquid discharging unit (1006) via the first set of openings (1008). Therefore, the new corresponding amount of liquid to be discharged is also stored in the database (1014).

[53] Depending on the number of times the new threshold is revised, over a period of predefined time for a patient, the training module (1004) records the progress of the patent.

[54] The database (1014) also stores, including but not limited to, amount of vaginal secretion, amount of blood secretion, pH-level of the vaginal secretion, pH- level of the blood secretion, a length of change in colour of the first part (100) and value of change in the length of the vaginal passage with respect to the first part

(100).

[55] Similar to the first part (100), when the second part (200) of the vaginal exerciser is positioned in the vaginal passage, the plurality of internal vaginalmuscles of the vaginal passage contract, thereby applying a second linear force to the second part (200) by the contraction of the plurality of internal vaginal muscles. In one embodiment, the second linear direction may be representative of a vertical direction in which the force is applied by the contraction of the plurality of internal vaginal muscles to the second part (200) of the vaginal exerciser.

[56] The second part (200) is operatively coupled to the first part (100), wherein while the second part (200) of the vaginal exerciser is inserted into the vaginal passage of the patient, the patient tries to contract the plurality of internal vaginal muscles. Upon the contraction of the plurality of internal vaginal muscles, the second set of sensors (1018) sense a second amount of force applied to the second part (200) by the contraction of the plurality of internal vaginal muscles. In one embodiment, once the second part (200) is coupled with the first part (100), the training module (1004) deactivates the first set of sensors (1016)and activates the second set of sensors (1018). In another embodiment, the first part (100) may be coupled to the second part (200), wherein the user may choose to activate the first set of sensors (1016)and keep the second set of sensors (1018) in an inactive mode, thereby using the second part (200) as a support in the vaginal passage.

[57] In one embodiment, the second part (200) may be of a phallus shaped, wherein the second part is inserted into the vaginal passage without the first part (100).

[58] The input module (1002) is configured to receive a second sensed data from the second set of sensors (1018) provided in the second part (200), wherein the second sensed data represents the second amount of force applied by the contraction of the plurality of internal vaginal muscles. The second sensed data is stored in the database (1014). The second sensed data is also provided to the training module (1004), wherein the training module (1004) analyses the second sensed data. A second threshold values set based on received second sensed data by the medical practitioner corresponding to the patient, wherein the second threshold level set for the corresponding patient is stored in the database (1014). [59] Based on the second amount of force encountered by the second part (200) of the vaginal exerciser, the liquid discharging unit (1006)is configured to discharge a corresponding second amount of liquid into the vaginal passage via the second set of openings (1010).

[60] For example, say there are ten levels of second amount of force that could be applied to the second part (200). If a second level of second amount of force is applied to the second part (200) of the vaginal exerciser, then the second part (200) discharges a second amount of liquid via the second set of openings (1010), into the vaginal passage, corresponding to the second level of force applied to the second part (200). Similarly, if a sixth level or a tenth level of force is applied to the second part (200), then the second part (200) discharges a second amount of liquid via the second set of openings (1010), into the vaginal passage, corresponding to the sixth level or the tenth level of force applied to the one or more adhesions. At least one value of the second amount of force applied, and at least one value of the corresponding amount of liquid discharged is stored in the database (1014). Therefore, for each patient, different levels of force that is the threshold levels, applied to the second part (200) of the vaginal exerciser in corresponding patients is stored in the database (1014), thereby building a personalised support module for each patient.

[61] In one embodiment, the database (1014) also stores, including but not limited to, amount of vaginal secretion, pH-level of the vaginal secretion, a length of change in colour of the second part (200) and value of change in the length of the vaginal passage with respect to the second part (200).

[62] The third part (300) includes the plurality of vibrators (1012), wherein the third part (300)is configured to be placed on the outside of the vaginal passage, that is the plurality of external vaginal muscles. The patient is enabled by the interface unit (1000) to choose from a plurality of vibrating levels, wherein the patient’s choice of a vibrating level from the plurality of vibrating levels is received by the input module (1002). The patient’s choice from the plurality of vibrating levels is stored in the database (1014).

[63] The support unit (600) is operatively coupled to the vaginal exerciser, wherein the support unit (600) is a handle. In one embodiment, the support unit (600) may include, but not limited to, the actuator and a power supply unit (not shown in figures), wherein the actuator may be the motor. In another embodiment, the support unit (600) may also include, but not limited to, the processor, the interface unit (1000) and a display unit (not shown in figures).

[64] Further, the vaginal exerciser may be provided with a provision (not shown in figures) of supplying oxygen into the vaginal passage, wherein the oxygen supply is configured to prevent new adhesions from forming in the vaginal passage.

[65] Further, the training module (1004) includes a tracking module (1020, FIG. 2), wherein the training module (1004) is operatively coupled to the tracking module (1020). The tracking module (1020) is configured to track progress achieved by the patient, wherein the progress achieved by the user is based on, including but not limited to, the first sensed data, the second sensed data, the revised first and second threshold, respectively, reduction in liquid from the first part (100) and second part (200), reduction in one or more adhesions and, achieved toned plurality of internal and external vaginal muscles.

[66] Further, the training module (1004) also includes a notification module (1022), wherein the training module (1004) is operatively coupled to the notification module (1022). The notification module (1022) is configured to notify, via a communication module (not shown in figures), including but not limited to, tracked data and analysed data to, including but not limited to, the medical practitioner and/or the patient. The tracked data represents, including but not limited to, the first sensed data, the second sensed data, the revised first and second threshold, respectively, reduction in liquid from the first part (100) and second part (200), reduction in one or more adhesions, achieved toned plurality of internal and external vaginal muscles. The analysed data represents data utilized to build the personalised the support model. The medical practitioner and/or patient are notified in the form of, including but not limited to, reports, wherein the reports are notified to the medical practitioner and/or the patient via, including but not limited to, an email, a text message and a provision for the user, that is patient and the medical practitioner, to receive at least one notification via the internet. For example, the provision represents hospital website wherein the patient is enabled to retrieve medical reports, from the database (1014), provided by the medical practitioner.

[67] Further, the notification module (1022) also notifies the medical practitioner and/or the patient if there is no sufficient liquid in the first part (100) and/or second part (200) of the vaginal exerciser, wherein training module (1004)is configured to check if there is sufficient liquid in the first part (100) and/or second part (200) of the vaginal exerciser. The processor is operatively coupled to the training module (1004) and the interface unit (1000).

[68] Further, the training module (1004) includes an error management module (not shown in figures) is configured to check the statuses of the components present in vaginal exerciser, wherein the components are, including but not limited to, the first set of sensors, the second set of sensors (1018), the liquid discharging unit (1006)and the communication module. The error management module is configured to alert the user if the training module (1004) detects the first set of sensors, second set of sensors (1018) and the plurality of vibrators (1012) to be inactive when the user selects at least one option from the one or more options. Further, the error management module is also configured to alert the user if one or more of the sensors from the first set of sensors (1016) and the second set of sensors (1018) are not functioning. Similarly, the error management module is configured to alert the user if one of the vibrators from the plurality of vibrators (1012) are not functioning.

[69] Further, the error management module is also configured to assess the conditions of the first set of openings (1008) and the second set of openings (1010). If the error management module detects, including but not limited to, blockage of one or more of the first set of openings (1008) and the second set of openings (1010), the error management module alerts the user of the same.

[70] Further, the error management module is also configured to check the condition of, including but not limited to, the actuator. If any malfunction is detected, then the user is alerted of the same by the error management module.

[71] In one embodiment, if the user does not select any option displayed to the user, where the user decision is required, then the error management module may temporarily shut down the system.

[72] Further, the error management module is also configured to alert the user the time of cleaning, wherein the user is enabled to select a time and time duration of cleaning of the vaginal exerciser. In one embodiment, if the error management module detects the statuses of the components of the vaginal exerciser to be in a functioning condition, then the error management module initiates the cleaning process. In another embodiment, the error management module may wait for predefined time duration before initiating the cleaning process of the vaginal exerciser after the vaginal exerciser is used by the user. [73] Further, the training module (1004) includes a hibernation mode, wherein the training module activates the hibernation mode for the purposes of, including but not limited to, rebuilding or reopening the vaginal passage of the patient. In the hibernation mode, for rebuilding the vaginal passage, the training module (1004) may only activate the liquid discharging unit, wherein the liquid discharging unit (1006)is configured to push the liquid out of the vaginal exerciser. In one embodiment, the liquid discharging unit (1006) may push out the liquid of the vaginal exerciser at a predefined time interval.

[74] Further, the system includes a display unit, wherein the display unit is configured to display, including but not limited to, the amount of force applied by the first part (100), the amount of force applied to the second part (200), the amount of liquid discharged by the at least one of the first part (100) and the second part (200), and the plurality of vibrating levels provided for the plurality of vibrators (1012). The display unit also displays, including but not limited, to one or more apparatus configuration settings, such as, including but not limited to, saving options for patient treatment data, new treatment options, alerts and connection settings.

[75] FIG. 2 illustrates an exemplary embodiment of the system for vaginal assessment in accordance with an embodiment of the present disclosure. The system (10) includes an interface unit (1000), wherein the interface unit (1000) is operatively coupled to a vaginal exerciser.

[76] The interface unit (1000) enables the user, that is the medical practitioner and/or the patient, to select one or more options via a display of the display unit, wherein the one or more options are, including but not limited to, the first part (100), the second part (200) and the third part (300). In one embodiment, the first part (100) may represent treatment, wherein the treatment may represent breaking the one or more adhesions in the vaginal passage of the patient, the second part (200) may represent exercising of the plurality of the internal vaginal passage and the third part (300) may represent toning of the plurality of external vaginal muscles.

[77] In one embodiment, the user selects the first part (100), that is the treatment, then the training module (1004) checks if the first set of sensors (1016)of the first part (100) of the vaginal exerciser are activated. If the first set of sensors (1016)are activated, then the training module (1004)provides a first set of options to the user to choose from, wherein the first set of options may be, including but not limited to, data collection such as including but not limited to, present clinical data and historical clinical data. The present clinical data may be defined as the data analysed and stored in the database in real time while using the first part (100) of the vaginal exerciser. The historical clinical data may be defined as previously analysed data and stored in the database when the first part (100) of the vaginal exerciser was used by the user prior to current usage.

[78] In one embodiment, if the patient is using the vaginal exerciser for a first time, then there is no historical clinical data available in the database (1014) for the training module (1004) to compare the current clinical data with. Therefore, the current clinical data is analysed by the training module (1004) and stored in the database (1014).

[79] Once the user selects at least one option from the first set of options, the training module (1004) checks with the user if the first set threshold needs to be set while using the first part (100) of the vaginal exerciser for the first time.

[80] Once the user starts to begin inserting the first part (100) of the vaginal exerciser into the vaginal passage, the first part (100) upon contacting the one or more adhesions, the first set of sensors (1016) sense the first amount of force applied to the one or more adhesions by the medical practitioner. The first set of sensors (1016) send the first sensed data to the training module (1004), wherein the training module (1004) analyses the first sensed data. If the training module (1004) analyses that the first amount of force is greater than the first threshold value, then the training module (1004) checks with the medical practitioner if the first threshold value needs to be applied or if the amount greater than the first threshold value needs to be applied. Depending on the option the medical practitioner selects, the training module (1004) signals the liquid discharging unit (1006), wherein the liquid discharging unit (1006) includes the motor. The motor is activated upon receiving the signal from the training module (1004), wherein the motor, based on the option selected by the medical practitioner, moves the plunger rod forward in the first part (100), thereby discharging an amount of liquid corresponding to the option chosen by the medical practitioner into the vaginal passage via the first set of openings (1008), wherein the amount greater than the first threshold value and the amount of the liquid discharged is stored in the database (1014).

[81] In one embodiment, the training module (1004) compares the received first sensed data with the first threshold value. If the received first sensed data results to be lesser than the first threshold value, then the received first sensed data is analysed, by the training module (1004), to be a progress made by the patient.

[82] In one embodiment, the training module (1004)checks with the medical practitioner if the received first sensed data to be changed to a new threshold for first part (100) of the vaginal exerciser.

[83] In one embodiment, if the user selects the second part (200), that is the exercising of the plurality of internal vaginal muscles, from the one or more options, the second set of options displayed to the user, then the training module (1004) checks if the second set of sensors (1018) are activated.

[84] Once the second set of sensors (1018) are activated, then the training module (1004) requests the patient to select, including but not limited to, an exercise stage from a plurality of exercise stages, a predefined time duration and at least one target levels to be reached. Depending on the option selected by the patient, the training module (1004) further requests the patient to provide data for data collection, then the training module (1004) provides a third set of options to the user to choose from, wherein the third set of options may be, including but not limited to, data collection such as including but not limited to, present clinical data and historical clinical data. The present clinical data may be defined as the data analysed and stored in the database in real time while using the second part (200) of the vaginal exerciser. The historical clinical data may be defined as previously analysed data and stored in the database (1014) when the second part (200) of the vaginal exerciser was used by the user prior to current usage.

[85] In one embodiment, if the patient is using the vaginal exerciser for a first time, then is no historical clinical data available in the database for the training module (1004) to compare the current clinical data with. Therefore, the current clinical data is analysed by the training module (1004) and stored in the database (1014).

[86] Once the patient has positioned the second part (200) in the vaginal passage, upon contraction of the internal vaginal muscles, the second set of sensors (1018) sense the second amount of force applied to the second part (200) by the contracting of the plurality of internal vaginal muscles. The second set of sensors (1018)send the second sensed data to the training module (1004) to analyse the second sensed data, wherein the second sensed data represents the second amount of force applied to the second part (200). Depending on the received second sensed data, the liquid discharging unit (1006)is configured to discharge an amount of liquid into the vaginal passage, via the second set of openings (1010), corresponding to the received second sensed data. The training module (1004) receives the second sensed data from the second set of sensors (1018) and analyses received second sensed data, wherein the value of the received second sensed data and the value of the amount of liquid discharged is stored in the database (1014).

[87] In one embodiment, depending on the received second sensed data, the second part (200) is configured to discharge an amount of liquid into the vaginal passage, via the second set of openings, corresponding to the received second sensed data.

[88] In one embodiment, the training module (1004) compares the received second sensed data with the second threshold value. If the received second sensed data results to be greater than the second threshold value, then the received second sensed data is analysed, by the training module (1004), to be a progress made by the patient. If the received sensed data results to be less than the second threshold value, then the training module (1004) alerts the user. The value of the received second sensed data which is less than the second threshold value is stored in the database.

[89] In one embodiment, if the received second sensed data is greater that second threshold value, the training module (1004) checks with the medical practitioner if the second threshold value is to be changed to a new threshold for second part (200) of the vaginal exerciser corresponding to the received second sensed data which is greater than the second threshold value.

[90] In one embodiment, the user may select the third part (300), that is the toning of the plurality of external vaginal muscles, from the one or more option displayed via the displayed unit. The training module (1004) checks if the plurality of vibrators (1012) present in the third part (300)is activated, wherein once the plurality of vibrators (1012) is activated, then the training module (1004) requests the patient to select from a fourth set of options, including but not limited to, data collection, such as, including but not limited to, present clinical data and historical clinical data. The present clinical data may be defined as the data analysed and stored in the database in real time while using the vaginal exerciser. The historical clinical data may be defined as previously analysed data and stored in the database when the third part (300) of vaginal exerciser was used by the user prior to current usage. The patient is provided, by the display unit, with the plurality of vibrating levels and a plurality of time durations to select at least one vibrating level and at least one time duration.

[91] Once the patient has placed the third part (300) against the plurality of external vaginal muscles, the patient selects one of the levels from the plurality of vibrating levels and a time duration from the plurality of time durations, via the display. The training module (1004) analyses the selected vibrating level and compares the selected vibrating level with the third threshold value, wherein the training module (1004) checks with the patient if the selected level is to be applied or third threshold value to be applied. Depending on the patient’s selection, the plurality of vibrators (1012) is vibrated at a level corresponding to the patient’s selection for the selected time duration. The user is enabled to select one of the vibrating levels from the plurality of vibrating levels, wherein the higher the selected vibrating level, the weaker the plurality of vaginal external muscles are. The training module (1004) analyses the selected vibrating level based on which the strengthening or toning of the plurality of external vaginal muscles are tracked and stored in the database (1014).

[92] Further, The tracking module (1020) is configured to track progress achieved by the patient, wherein the progress achieved by the user is based on, including but not limited to, the first sensed data, the second sensed data, the revised first and second threshold, respectively, reduction in liquid from the first part (100) and second part (200), reduction in one or more adhesions and, achieved toned plurality of internal and external vaginal muscles.

[93] Further, the notification module (1022) is configured to notify, via a communication module (not shown in figures), including but not limited to, tracked data and analysed data to, including but not limited to, the medical practitioner and/or the patient. The analysed data represents data utilized to build the personalised the support model. The medical practitioner and/or patient are notified in the form of, including but not limited to, reports, wherein the reports are notified to the medical practitioner and/or the patient via, including but not limited to, an email and a text message and a provision for the user, that is patient and the medical practitioner, to receive at least one notification via the internet. For example, the provision represents hospital website wherein the patient is enabled to retrieve medical reports, from the database (1014), provided by the medical practitioner. [94] FIG. 3 illustrates a block level diagram of a system (20) for vaginal assessment in accordance with an embodiment of the present invention.

[95] The system (20) includes processor(s) (26), bus (24) and memory (22) coupled to the processor(s) (26) via the bus (24), and the database (1014, FIG.2).

[96] The processor(s) (26), as used herein, means any type of computational circuit, such as, but not limited to, a microprocessor, a microcontroller, a complex instruction set computing microprocessor, a reduced instruction set computing microprocessor, a very long instruction word microprocessor, an explicitly parallel instruction computing microprocessor, a digital signal processor, or any other type of processing circuit, or a combination thereof.

[97] The bus, as used herein, is a communication system that transfers data between components inside a computer, or between computers.

[98] The memory (22) includes a plurality of modules stored in the form of executable program which instructs the processor (26) to perform the method steps illustrated in Figure 1. The memory (22) has following modules: an interface unit (1000), wherein the interface unit (1000) includes an input module (1002), a training module (1004) and a liquid discharging unit (1006).

[99] Computer memory elements may include any suitable memory device(s) for storing data and executable program, such as read only memory, random access memory, erasable programmable read only memory, electrically erasable programmable read only memory, hard drive, removable media drive for handling memory cards and the like. Embodiments of the present subject matter may be implemented in conjunction with program modules, including functions, procedures, data structures, and application programs, for performing tasks, or defining abstract data types or low-level hardware contexts. Executable program stored on any of the above-mentioned storage media may be executable by the processor(s) (26).

[100] The interface unit (1000) is operatively coupled to the vaginal exerciser.

[101] The input module (1002) is configured to receive the first sensed data and the second sensed data from the first set of sensors (1016)and the second set of sensors (1018) provided in the vaginal exerciser, wherein the first sensed data represents a first amount of external force applied, by the vaginal exerciser, to a corresponding adhesion formed in a vaginal passage and the second sensed data represents the second amount of force applied by contraction of a plurality of muscles of the vaginal passage to the vaginal exerciser. [102] The training module (1004) is configured to analyse at least one of the first sensed data and the second sensed data received from the input module (1002) based on a corresponding threshold data, wherein the corresponding threshold data comprises one or more forces applied by the external force and the contraction of the one or more vaginal muscles. The training module also analyses the at least one vibrating level received from the input. Based on the analysed data, the training module is further configured to build a personalised support model for vaginal exercise based on analysed data.

[103] The liquid discharging unit (1006) is configured to discharge, via an actuator, liquid corresponding to the personalised support model for the vaginal exercise.

[104] FIG. 4 illustrates a flow chart representing steps involved in a method (30) for vaginal assessment in accordance with an embodiment of the present disclosure.

[105] The method (30) includes receiving a first sensed data, in step 32. The method (30) includes receiving, by an input module (1002), a first sensed data from a first set of sensors (1016) provided in the vaginal exerciser, wherein the first sensed data comprises a first amount of force applied by a first part (100) of the vaginal exerciser to a corresponding adhesion formed in a vaginal passage. The first set of sensors (1016) is provided in a first part (100) of the vaginal exerciser. The first part (100) is configured to break one or more adhesions formed in a vaginal passage.

[106] When the first part (100) of the vaginal exerciser is being inserted into the vaginal passage of the patient, the first part (100) upon coming in contact with the one or more adhesions, the first set of sensors (1016)are configured to sense the first amount of force applied to the one or more adhesions formed in the vaginal passage applied by a user via the first part (100) of the vaginal exerciser. The user may be, including but not limited to, the patient and a medical practitioner.

[107] The input module (1002) is configured to receive first sensed data from the first set of sensors (1016)provided in the first part (100), wherein the first sensed data represents the first amount of force. The first amount of force is applied in a first linear direction by the user to a corresponding one or more adhesions formed in the vaginal passage. In one embodiment, the first linear direction may be representative of the horizontal direction in which the first part (100) of the vaginal exerciser is being inserted into the vaginal passage of the patient by the medical practitioner or the patient. [108] The first sensed data is stored in a database. The first sensed data is also provided to the training module (1004).

[109] The method (30) includes receiving a second sensed data, in step 34. The method (30) includes receiving, by the input module (1002), a second sensed data from a second set of sensors (1018) provided in the vaginal exerciser, wherein the second sensed data comprises a second amount of force applied by contraction of a plurality of muscles of vaginal passage to the vaginal exerciser.

[110] The second part (200) of the vaginal exerciser is positioned in the vaginal passage, wherein the plurality of internal vaginal muscles of the vaginal passage contract, thereby applying a second linear force to the second part (200) by the contraction of the plurality of internal muscles. In one embodiment, the second linear direction may be representative of the vertical direction in which force is applied by the contraction of the plurality of vaginal muscles to the second part (200) of the vaginal exerciser.

[111] When the second part (200) of the vaginal exerciser is inserted into the vaginal passage of the patient, the patient tries to contract the plurality of internal vaginal muscles. Upon the contraction of the plurality of internal vaginal muscles, the second set of sensors (1018) sense a second amount of force applied to the second part (200) by the contraction of the plurality of internal vaginal muscles.

[112] The input module (1002) is configured to receive a second sensed data from the second set of sensors (1018) provided in the second part (200), wherein the second sensed data represents the second amount of force applied by the contraction of the plurality of internal vaginal muscles. The second sensed data is stored in the database (1014).

[113] The method (30) includes analysing at least one of the first sensed data and the second sensed data, in step 36. The method (30) includes analysing, by a training module (1004), at least one of the first sensed data and the second sensed data received from the input module (1002) based on a first threshold value, wherein the first g threshold value comprises one or more forces applied by the external force and the contraction of the one or more vaginal muscles.

[114] The user is enabled, by an interface unit (1000), to select the first part (100) as an option via a display, wherein the first part (100) may represent treatment. The treatment may represent breaking the one or more adhesions in the vaginal passage of the patient. [115] The training module (1004) checks if the first set of sensors (1016)of the first part (100) of the vaginal exerciser are activated. If the first set of sensors (1016) is activated, then the training module (1004) provides a first set of options to the user to choose from, wherein the first set of options may be, including but not limited to, data collection such as including but not limited to, present clinical data and historical clinical data. The present clinical data may be defined as the clinical data analysed and stored in the database in real time while using the first part (100) of the vaginal exerciser. The historical clinical data may be defined as previously analysed data and stored in the database when the first part (100) of the vaginal exerciser was used by the user prior to current usage.

[116] Once the user selects at least one option from the first set of options, the training module (1004) checks with the user if the first threshold value needs to be set while using the first part (100) of the vaginal exerciser

[117] Once the user starts to begin inserting the first part (100) of the vaginal exerciser into the vaginal passage, the first part (100) upon contacting the one or more adhesions, the first set of sensors (1016) sense the first amount of force applied to the one or more adhesions by the medical practitioner. The first set of sensors (1016) send the first sensed data to the training module (1004), wherein the training module (1004) analyses the first sensed data. If the training module (1004) analyses that the first amount of force is greater than the first threshold value, then the training module (1004) checks with the medical practitioner if the first threshold value needs to be applied or if the amount greater than the first threshold value needs to be applied.

[118] The user selects the second part (200), that is the exercising of the plurality of internal vaginal muscles, from the one or more options, the second set of options displayed to the user, then the training module (1004) checks if the second set of sensors (1018) is activated. Once the second set of sensors (1018) are activated, then the training module (1004) requests the patient to select, including but not limited to, an exercise stage from a plurality of exercise stages, a time duration and at least one target levels to be reached. Depending on the option selected by the patient, the training module (1004) further requests the patient to provide data for data collection, then the training module (1004) provides a third set of options to the user to choose from, wherein the third set of options may be, including but not limited to, data collection such as including but not limited to, present clinical data and historical clinical data. The present clinical data may be defined as the clinical data analysed and stored in the database (1014) in real time while using the second part (200) of the vaginal exerciser. The historical clinical data may be defined as previously analysed data and stored in the database (1014) when the second part (200) of the vaginal exerciser was used by the user prior to current usage.

[119] Once the patient has positioned the second part (200) in the vaginal passage, upon contraction of the internal vaginal muscles, the second set of sensors (1018) sense the second amount of force applied to the second part (200) by the contracting of the plurality of internal vaginal muscles. The second set of sensors (1018) send the second sensed data to the training module (1004) to analyse the second sensed data, wherein the second sensed data represents the amount of force applied to the second part (200).

[120] The method (30) includes building a personalised support model, in step 38. The method (30) includes building, by the training module (1004), a personalised support model for vaginal exercise based on analysed data.

[121] The training module (1004) is configured to set the first threshold value upon analysing the first sensed data, wherein the first threshold value represents the first amount of force up to which the patient is capable of enduring.

[122] In one embodiment, the training module (1004) revises the first threshold value to the value of the additional amount of force and saves the revised threshold value in the database (1014), thereby revising the built personalised support model.

[123] In another embodiment, the training module (1004) enables the medical practitioner to select the additional amount of force as the revised threshold value or the medical practitioner may continue with the first threshold value, thereby revising the built personalised support model.

[124] The training module (1004) is configured to set the second threshold value upon analysing the second sensed data, wherein the second threshold value represents the second amount of force up to which the patient is capable of applying on the second part (200). In one embodiment, if the patient applies an additional amount of force than the second threshold value, then the training module (1004) compares the additional amount of force with the second threshold value. The value of the additional amount of force is stored in the database (1014).

[125] In one embodiment, the training module (1004) revises the second threshold value with the value of the additional amount of force and saves the revised threshold value in the database (1014), thereby revising the built personalised support model.

[126] In another embodiment, the training module (1004) enables the medical practitioner to select the additional amount of force as the revised threshold value or the medical practitioner may continue with the second threshold value, thereby revising the built personalised support model.

[127] The method (30) includes discharging liquid into the vaginal passage, in step 40. The method (30) includes discharging, by a liquid discharging unit (1006), via an actuator, liquid corresponding to the personalised support model for the vaginal exercise.

[128] In one embodiment, the liquid discharging unit (1006) may include, but not limited to, a plunger rod with a plunger tip and an actuator, wherein the plunger rod is operatively coupled to the actuator, wherein in one embodiment, the actuator may be a motor. The plunger rod is configured to pass through the vaginal exerciser, wherein the plunger rod is enabled to move to and fro in the vaginal exerciser. However, the movement of the plunger tip is limited within the first part (100) of the vaginal exerciser. In one embodiment, the movement of the plunger tip is limited within the second part (200) of the vaginal exerciser.

[129] The training module (1004) signals the motor to push the plunger rod forward corresponding to the first sensed data, wherein the plunger rod pushes corresponding amount of the liquid into the vaginal passage via the first set of openings.

[130] Once the user starts to begin inserting the first part (100) of the vaginal exerciser into the vaginal passage, the first part (100) upon contacting the one or more adhesions, the first set of sensors (1016) sense the first amount of force applied to the one or more adhesions by the medical practitioner. The first set of sensors (1016) send the first sensed data to the training module (1004), wherein the training module (1004) analyses the first sensed data. If the training module (1004) analyses that the first amount of force is greater than the first threshold value, then the training module (1004) checks with the medical practitioner if the first threshold value needs to be applied or if the amount greater than the first threshold value needs to be applied. Depending on the option the medical practitioner selects, the training module (1004) signals the liquid discharging unit (1006), wherein the liquid discharging unit (1006) includes the motor. The motor is activated upon receiving the signal from the training module (1004), wherein the motor, based on the option selected by the medical practitioner, moves the plunger rod forward in the first part (100) , thereby discharging an amount of liquid corresponding to the option chosen by the medical practitioner into the vaginal passage via the first set of openings, wherein the value of the amount greater than the first threshold value and the value of the amount of the liquid discharged is stored in the database (1014).

[131] Once the patient has positioned the second part (200) in the vaginal passage, upon contraction of the internal vaginal muscles, the second set of sensors (1018) sense the second amount of force applied to the second part (200) by the contracting of the plurality of internal vaginal muscles. The second set of sensors (1018) send the second sensed data to the training module (1004) to analyse the second sensed data, wherein the second sensed data represents the second amount of force applied to the second part (200). Depending on the received second sensed data, the liquid discharging unit (1006) is configured to discharge an amount of liquid into the vaginal passage, via the second set of openings, corresponding to the received second sensed data. The training module (1004) receives the second sensed data from the second set of sensors (1018) and analyses received second sensed data, wherein the value of the received second sensed data and the value of the amount of liquid discharged is stored in the database (1014).

[132] In one embodiment, depending on the received second sensed data, the second part (200) is configured to discharge an amount of liquid into the vaginal passage, via the second set of openings, corresponding to the received second sensed data.

[133] Further, the method (30) includes toning of plurality of external vaginal muscles. In one embodiment, the user may select the third part (300), that is the toning of the plurality of external vaginal muscles, from the one or more option displayed via the displayed unit. The training module (1004) checks if the plurality of vibrators (1012) present in the third part (300) is activated, wherein once the plurality of vibrators (1012) is activated, then the training module (1004) requests the patient to select from a fourth set of options, including but not limited to, clinical data collection, such as, including but not limited to, present clinical data and historical clinical data. The present clinical data may be defined as the data analysed and stored in the database (1014) in real time while using the vaginal exerciser. The historical clinical data may be defined as previously analysed data and stored in the database (1014) when the third part (300) of vaginal exerciser was used by the user prior to current usage. The patient is provided, by the display unit, with the plurality of vibrating levels and a plurality of time durations to select at least one vibrating level and at least one time duration.

[134] Once the patient has placed the third part (300) against the plurality of external vaginal muscles, the patient selects one of the levels from the plurality of vibrating levels and a time duration from the plurality of time durations. The training module (1004) analyses the selected vibrating level and compares the selected vibrating level with the third threshold value, wherein the training module (1004) checks with the patient if the selected level is to be applied or the third threshold value to be applied. Depending on the patient’s selection, the plurality of vibrators (1012) is vibrated at a level corresponding to the patient’s selection for the selected time duration.

[135] Further, the method (30) includes tracking, by a tracking module (1020), progress achieved by a user, wherein tracking progress achieved by the user is based on, including but not limited to, the first sensed data, the second sensed data, the revised first and second threshold, respectively, reduction in liquid from the first part (100) and the second part (200), reduction in one or more adhesions, achieved toned plurality of internal and external vaginal muscles.

[136] Further, the method (30) includes notifying, by a notification module (1022), via a communication module, at least one of tracked data and the analysed data to the patient and/or the medical practitioner.

[137] The training module (1004) also includes a notification module (1022), wherein the training module (1004) is operatively coupled to the notification module (1022). The notification module (1022) is configured to notify, including but not limited to, tracked data and analysed data to, including but not limited to, the medical practitioner and/or the patient. The analysed data represents data utilized to build the personalised the support model. The medical practitioner and/or patient are notified in the form of, including but not limited to, reports, wherein the reports are notified to the medical practitioner and/or the patient via, including but not limited to, an email, a text message and a provision for the user, that is patient and the medical practitioner, to receive at least one notification via the internet. For example, the provision represents hospital website wherein the patient is enabled to retrieve medical reports, from the database (1014), provided by the medical practitioner. [138] The notification module (1022) also notifies the medical practitioner and/or the patient if there is no sufficient liquid in the first part (100) and/or the second part (200) of the vaginal exerciser, wherein the training module (1004) is configured to check if there is sufficient liquid in the first part (100) and/or the second part (200) of the vaginal exerciser. The processor is operatively coupled to the training module (1004) and the interface unit (1000).

[139] Further, the method (30) also includes checking, via an error management module, statuses of the components present in vaginal exerciser, wherein the components are, including but not limited to, the first set of sensors, the second set of sensors (1018), the liquid discharging unit (1006) and the communication module.

[140] The method (30) also includes alerting, by the error management module, the user if the training module (1004) detects the first set of sensors, second set of sensors (1018) and the plurality of vibrators (1012) to be inactive when the user selects at least one option from the one or more options.

[141] The method (30) also includes alerting, by the error management module, the user if one or more of the sensors from the first set of sensors (1016)and the second set of sensors (1018) are not functioning. Similarly, the error management module is configured to alert the user if one of the vibrators from the plurality of vibrators (1012) are not functioning.

[142] The method (30) also includes assessing, by the error management module, the conditions of the first set of openings (1008) and the second set of openings (1010). If the error management module detects, including but not limited to, blockage of one or more of the first set of openings (1008) and the second set of openings (1010), the error management module alerts the user of the same.

[143] The method (30) also includes checking, by the error management module, the condition of, including but not limited to, the actuator. If any malfunction is detected, then the user is alerted of the same by the error management module.

[144] In one embodiment, if the user does not select any option displayed to the user, where the user decision is required, then the error management module may temporarily shut down the system.

[145] The method (30) also includes alerting, by the error management module, the user the time of cleaning, wherein the user is enabled to select a time and a time duration of cleaning of the vaginal exerciser. In one embodiment, if the error management module detects the statuses of the components of the vaginal exerciser to be in a functioning condition, then the error management module initiates the cleaning process. In another embodiment, the error management module may wait for predefined time duration before initiating the cleaning process of the vaginal exerciser after the vaginal exerciser is used by the user.

[146] The method (30) also includes activating, by the training module in a hibernation mode, wherein the training module activates the hibernation mode for the purposes of, including but not limited to, rebuilding or reopening the vaginal passage of the patient. In the hibernation mode, for rebuilding the vaginal passage, the training module (1004) may only activate, including not limited to, the liquid discharging unit (1006) and the first set of sensors (1016), wherein the liquid discharging unit (1006) is configured to push the liquid out of the vaginal exerciser. In one embodiment, the liquid discharging unit (1006) may push out the liquid of the vaginal exerciser based on the amount of force sensed by the first set of sensors (1016).

[147] The method (30) also includes displaying, by a display unit, including but not limited to, the amount of force applied by the first part (100), the amount of force applied to the second part (200), the amount of liquid discharged by the at least one of the first part (100) and the second part (200), and the plurality of vibrating levels provided for the plurality of vibrators (1012). The display unit also displays, including but not limited, to one or more apparatus configuration settings, such as, including but not limited to, saving options for patient treatment data, new treatment options, alerts and connection settings.

[148] Further, the training module (1004), after creating a Personalize module for a patient, may suggest to the medical practitioner at least one future course of treatment for a selected patient(s). In addition, the training module (1004) may predict at least one clinical pattern for cervical cancer treatment. In some cases, the medical practitioner may keep the system on an auto mode, observing the treatment of the patient(s), thereby provides ease in handling patient’s load as well as the system may help in increasing the quality of life of the patient(s) by reducing probabilities of linked complications, including but not limited to, fistula.

[149] In one embodiment, the medical practitioner may request the training module (1004) to present analytical modular view of a patient’s progress or failure. The training module (1004) after displaying at least one report may suggest a new course of treatment based on the analyses of at least one failure respect to the patient based on the patient’s personalize model. Therefore, the training module may guide/suggest/help the medical practitioner in providing expert treatment(s) to the patient(s) in challenging scenarios.

[150] The present disclosure provides various advantages, including but not limited to, help a patient get rid of adhesions without causing injuries, to help stiffen and strengthen the internal and external muscles of the patient’s vagina. Further, the present disclosure also provides for keeping a track of the patient’s progress and builds a personalised support model for each patient.

[151] While specific language has been used to describe the disclosure, any limitations arising on account of the same are not intended. As would be apparent to a person skilled in the art, various working modifications may be made to the method in order to implement the inventive concept as taught herein.

[152] The figures and the foregoing description give examples of embodiments. Those skilled in the art will appreciate that one or more of the described elements may well be combined into a single functional element. Alternatively, certain elements may be split into multiple functional elements. Elements from one embodiment may be added to another embodiment. For example, order of processes described herein may be changed and are not limited to the manner described herein. Moreover, the actions of any flow diagram need not be implemented in the order shown; nor do all of the acts need to be necessarily performed. Also, those acts that are not dependant on other acts may be performed in parallel with the other acts. The scope of embodiments is by no means limited by these specific examples.