- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06269016
Effect of Hip Strengthening Exercises and Pelvic Floor Exercises on Stress Urinary Incontinence in Postnatal Women
February 17, 2024 updated by: Mai Mohamed Sherif Mohamed Hassan, Cairo University
this study will investigate effect of hip strengthening exercises and pelvic floor exercises on stress urinary incontinence in postnatal women.
Clinical practice guidelines recommend PFMT as the first-line treatment for female SUI .
Also, it has been speculated that the hip muscles are involved in the continence mechanism and that their deficiency could destabilize the normal function of the system.
The addition of hip muscle exercises, regardless of PFM contractions, aimed to improve muscular condition for the motor or synergic strategies in PFM contraction.
Secondary effects of these techniques, such as the influence of passive lumbar rotational mobilization in improving hip flexor strength, have been of high interest in physiotherapy in general
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
120
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Cairo, Egypt
- Mai Mohamed Sherif Mohamed Hassan
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Their ages will be ranged from 30 to 35 years old.
- Their BMI will not exceed 35 Kg/m2.
- All patients will be multipara women.
- Their deliveries were normal vaginal delivery.
- All patients will be diagnosed by gynecologist as mild or moderate degree of SUI.
- All patients will have the same medical treatment and free from any pathological conditions that might affect the result.
Exclusion Criteria:
- Recurrent urinary tract infections.
- Hypertension.
- Diabetes mellitus.
- Intra uterine device.
- Hysterectomy.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: control group no intervention
no intervention for 3 months with assessment for maximum vaginal squeeze pre and post experiment using bio feedback device and urinary distress inventory UDI-6 short form.
|
effect of strengthening exercise of combined hip strengthening exercises and pelvic floor exercises
|
Experimental: study group hip muscles strengthening exercise.
hip muscles exercises (hip abductors, adductors and gluteus maximus) for 3 months with assessment for maximum vaginal squeeze pre and post experiment using bio feedback device and urinary distress inventory UDI-6 short form.
|
effect of strengthening exercise of combined hip strengthening exercises and pelvic floor exercises
|
Experimental: study group hip muscles strengthening exercise combined with pelvic floor muscles exercise.
hip muscles exercises (hip abductors, adductors and gluteus maximus) combined with pelvic floor muscles exercises for 3 months with assessment for maximum vaginal squeeze pre and post experiment using bio feedback device and urinary distress inventory UDI-6 short form.
|
effect of strengthening exercise of combined hip strengthening exercises and pelvic floor exercises
|
Experimental: study group pelvic floor muscles exercise.
pelvic floor muscles exercises for 3 months with assessment for maximum vaginal squeeze pre and post experiment using bio feedback device and urinary distress inventory UDI-6 short form.
|
effect of strengthening exercise of combined hip strengthening exercises and pelvic floor exercises
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
hip muscles strengthening exercise.
Time Frame: 3 months
|
measure the muscle power and endurance for pelvic floor muscles by using bio feedback device to measure maximum vaginal squeeze
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 20, 2023
Primary Completion (Actual)
August 25, 2023
Study Completion (Estimated)
April 20, 2024
Study Registration Dates
First Submitted
January 27, 2024
First Submitted That Met QC Criteria
February 17, 2024
First Posted (Estimated)
February 21, 2024
Study Record Updates
Last Update Posted (Estimated)
February 21, 2024
Last Update Submitted That Met QC Criteria
February 17, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Behavioral Symptoms
- Mental Disorders
- Urologic Diseases
- Lower Urinary Tract Symptoms
- Urological Manifestations
- Urination Disorders
- Elimination Disorders
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Urogenital Diseases
- Male Urogenital Diseases
- Urinary Incontinence
- Enuresis
- Urinary Incontinence, Stress
Other Study ID Numbers
- P.T.REC/012/003888
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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