Kegel Exercises for Stress Urinary Incontinence

NCT ID: NCT05529238

Last Updated: 2023-02-08

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

29 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-06-18

Study Completion Date

2019-08-18

Brief Summary

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Study about a targeted group of women suffering from self-reported stress urinary incontinence, attend a Kegel exercise training program. The group was divided into two; supervised and unsupervised. Whilst both groups benefited from initially seeing a women's health physiotherapist for a pelvic floor muscle assessment and a bespoke Kegel exercise program, only the supervised group continued to see the physiotherapist for monthly bio-feedback training. The unsupervised group relied on their own motivation to perform their Kegel exercises as prescribed. At the end of the twelve week program, both groups had a final pelvic floor muscle strength assessment by the physiotherapist to determine any changes and subsequent improvements in urinary incontinence.

Aim : Investigate and compare the efficacy of supervised Kegel exercises with biofeedback on Stress Urinary Incontinence (SUI) and Pelvic Floor Muscle Strength (PFMS) compared to unsupervised Kegel exercises.

The primary goal of this study was to determine the effectiveness of supervised Kegel exercises using BT versus unsupervised Kegel exercises without biofeedback training, on SUI. A secondary outcome was to establish whether an improvement was observed in PFMS and subsequently, the effect of this on SUI. It was hypothesized that regular support and visual motivation and direction of BT from the physiotherapist, would provide greater results.

Detailed Description

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Conditions

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Urinary Incontinence,Stress

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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supervised group during study

monthly physiotherapist appointment for half of the cohort including pelvic floor examination by physiotherapist including digital palpation and perineometry.

Group Type OTHER

biofeedback training

Intervention Type BEHAVIORAL

participants received biofeedback training for kegel exercises in the supervised group. the unsupervised group practised their Kegel exercises at home

unsupervised group during study

No intervention. Participants to practice kegel exercises at home.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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biofeedback training

participants received biofeedback training for kegel exercises in the supervised group. the unsupervised group practised their Kegel exercises at home

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* being female
* aged over 18 years
* suffer from SUI (their subjective disclosure was based on a description provided for their reference)
* did not perform Kegel exercises
* be available for duration of 12-week program

Exclusion Criteria

* pregnancy and breastfeeding
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Charles Darwin University

OTHER

Sponsor Role lead

Responsible Party

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Donelle Cross

Lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Charles Darwin University

Darwin, Northern Territory, Australia

Site Status

Countries

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Australia

Other Identifiers

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Interventional

Identifier Type: -

Identifier Source: org_study_id

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