Pelvic Floor Dysfunction and Quality of Life in Patient Undergoing Gynecological Surgery

NCT ID: NCT06875635

Last Updated: 2025-12-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-04-25

Study Completion Date

2025-11-25

Brief Summary

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The purpose of the study is to assess the pelvic floor dysfunction and quality of life in patient undergoing gynecological surgery.Common gynecological surgeries done for prolapse, fibroids, and cervical abnormality and also for Gynecological cancer.Early physiotherapy after gynecological surgery improves recovery by managing pain, restoring movement, and strengthening muscles, especially the pelvic floor.Conservative treatments like pelvic floor muscle exercises, biofeedback, and lifestyle changes can help with pelvic symptoms, including urinary incontinence and mild to moderate prolapse.

Detailed Description

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This is a randomized control trial to see the effects of pelvic floor training on pelvic floor dysfunction and quality of life in patient undergoing gynecological surgery. Females meeting the inclusion and exclusion criteria will be divided into three groups by convenient sampling technique. A sample size of 48 females with 16 females in each group. Group A will be treated four weeks pre and 8 weeks post op pelvic floor training exercises, group B will be treated only 8 weeks post op pelvic floor training exercises and group C will receive basic post op nursing care. Group A and B will have three treatment sessions per week Assessment will be done at 0 week (1month prior to surgery), 1 day before surgery, 2nd , 4th, 6th and 8th week after surgery. Females will be screened by Pelvic organ distress inventory (PFDI-20) and Pelvic floor impact questionnaire (PFIQ-7).

Conditions

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Pelvic Floor Dysfunction

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

There will be comparison between 3 groups.Two intervention group and 1 control group
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Investigators
The Principal investigator or the researcher will be kept blind about the group allocation and intervention or assessment of patients.

Study Groups

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Prepost PFMT Group

Routine medical care and pre \& post-op - op protocol of pelvic floor muscle training .1 month prior and 8 weeks post op protocol in patient undergoing gynecological surgery

Group Type EXPERIMENTAL

Pre and Post op pelvic floor muscle training

Intervention Type OTHER

pre op exercises: Breathing exercise ,Kegel exercise ,Abdominals exercise include pelvic tilt ,knee rolling with abdominal contraction post op exercise :breathing exercise, circulatory exercise i.e ankle pump and heel slides, and bed mobility along with pre op exercise

Post PFMT Group

Only Post-op pelvic floor muscle training for 8 weeks along with Routine medical care

Group Type EXPERIMENTAL

Only post op pelvic floor muscle training

Intervention Type OTHER

post op exercise :breathing exercise, circulatory exercise i.e ankle pump and heel slides, and bed mobility along with pre op protocol

Control

Routine medical care was given

Group Type OTHER

Routine medical care

Intervention Type OTHER

Circulatory exercise Breathing exercise Administrating analgesic Nursing care

Interventions

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Pre and Post op pelvic floor muscle training

pre op exercises: Breathing exercise ,Kegel exercise ,Abdominals exercise include pelvic tilt ,knee rolling with abdominal contraction post op exercise :breathing exercise, circulatory exercise i.e ankle pump and heel slides, and bed mobility along with pre op exercise

Intervention Type OTHER

Only post op pelvic floor muscle training

post op exercise :breathing exercise, circulatory exercise i.e ankle pump and heel slides, and bed mobility along with pre op protocol

Intervention Type OTHER

Routine medical care

Circulatory exercise Breathing exercise Administrating analgesic Nursing care

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Women age:40 -60yrs
* undergoing vaginal or laparoscopic-assisted vaginal surgery for either POP repair (primary or recurrent), and/or hysterectomy

Exclusion Criteria

* Emergency Surgery
* Chronic Illness
* Unstable Mental State
Minimum Eligible Age

40 Years

Maximum Eligible Age

60 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Riphah International University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Huma Riaz, PhD

Role: PRINCIPAL_INVESTIGATOR

Riphah International University, Islamabad, Pakistan

Locations

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Lady Reading Hospital MTI

Peshawar, KPK, Pakistan

Site Status

Countries

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Pakistan

Other Identifiers

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Majida zaffar

Identifier Type: -

Identifier Source: org_study_id

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