Kegel Exercises Prior to Strength Training to Improvestress Urinary Incontinence

NCT ID: NCT05527639

Last Updated: 2023-08-07

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

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-05-18

Study Completion Date

2019-12-18

Brief Summary

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This comparative pre-post intervention study investigates the feasibility and benefits of Kegel exercises amongst incontinent women, prior to commencing resistance training, to reduce the risk of stress urinary incontinence compared to a group of women without prior Kegel exercises.

Detailed Description

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The aim of the study is to determine whether a program of Kegel exercises prior to a resistance training program will result in reduction of stress urinary incontinence and whether this should be prescribed to incontinent women prior to performing resistance training. It is hypothesized that performing kegel exercises prior to resistance training would improve pelvic floor muscle strength and reduces the odds of experiencing SUI during resistance training.

Conditions

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Urinary Incontinence,Stress

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

A comparative study using data from 2 separate studies. Data used for the resistance training (RT) group from a foundational single cohort that investigated impact of RT on stress urinary incontinence (SUI) in a group of women participating in a RT program who had not previously done Kegel exercises (KE). New data for the KE+RT group was from 2 consecutive studies where the women completed a program of supervised / unsupervised KE. These 19 women took part in 12 weeks of RT to compare against the KE group. The findings of two separate studies in which the effect of RT on SUI and pelvic floor muscle strength was compared between women who completed 12 weeks of RT with or without prior KE. The RT group consisted of 14 women who did not have an experience in RT or KE and completed 12 weeks of RT. Women in the KE plus RT group (n=19) completed 12 weeks of Kegel exercise under the supervision of a qualified pelvic floor specialist; then completed the identical RT program as the RT group
Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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intervention group during study

all participants completed a 12 week strength training program consisting of warm up exercises, dead-lifts and squats. They had all completed a program of Kegel exercise prior.

Group Type OTHER

strength training program

Intervention Type BEHAVIORAL

12-weeks of strength training consisting of warm ups, dead-lifts, squats and cool down exercises

control group during study

all participants completed a 12 week strength training program consisting of warm up exercises, dead-lifts and squats

Group Type OTHER

strength training program

Intervention Type BEHAVIORAL

12-weeks of strength training consisting of warm ups, dead-lifts, squats and cool down exercises

Interventions

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strength training program

12-weeks of strength training consisting of warm ups, dead-lifts, squats and cool down exercises

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* being female
* over eighteen years of age
* suffer from stress urinary incontinence
* did not perform Kegel exercises
* had no experience in regular resistance/strength training
* completed a physical activity readiness questionnaire (PAR-Q) form.

Exclusion Criteria

* pregnancy, 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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CharlesDarwinU

Identifier Type: -

Identifier Source: org_study_id

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