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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05527639
Other study ID # CharlesDarwinU
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 18, 2019
Est. completion date December 18, 2019

Study information

Verified date August 2023
Source Charles Darwin University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date December 18, 2019
Est. primary completion date December 18, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

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

Locations

Country Name City State
Australia Charles Darwin University Darwin Northern Territory

Sponsors (1)

Lead Sponsor Collaborator
Charles Darwin University

Country where clinical trial is conducted

Australia, 

Outcome

Type Measure Description Time frame Safety issue
Primary incontinence severity index (ISI) tool questionnaire for self-reported frequency and severity of urinary incontinence. the higher the score, the higher the impact of incontinence Week 0
Primary incontinence severity index (ISI) tool questionnaire for self-reported frequency and severity of urinary incontinence. the higher the score, the higher the impact of incontinence Week 12
Primary pelvic floor muscle strength physiotherapist report from digital palpation and perineometry week 0
Primary pelvic floor muscle strength physiotherapist report from digital palpation and perineometry week 12
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