- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06924905
Exploring Pelvic Floor Dysfunction Among Egyptian Female Athletes
Exploring Pelvic Floor Dysfunction Among Egyptian Female Athletes: Prevalence, Risk Factors, and Implications for Performance
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
RESEARCH QUESTION:
Is there high prevalence of pelvic floor dysfunction among athletic females in Egypt and if there is specific sports contributing to that? the Sample are the Females recruited from different clubs across Egypt, female athletes who participated in previous studies and got thier contact and consent and by a Google form sent via links through social media aiming to reach a wide varieties of athletes across egypt . They will be selected according to the following eligibility criteria. the pelvic floor disability index will be used to evaluate pelvic floor. The questionnaire, transferred to Google Form, consists of 20 questions divided into three sections: Pelvic Organ prolapse Distress Inventory 6 (POPDI-6), Colorectal-Anal distress Inventory 8 (CRAD-8) and Urinary distress Inventory 6 (UDI-6). Fifteen participants, randomly selected by administrative staff, academics, and students of the Faculty of Physiotherapy at Cairo University, will test the questionnaire to identify any issues with language or format.
Data will be analyzed using IBM SPSS (version 22) for Windows. Demographic data will be analyzed using ANOVA. Bivariate correlation will be used to assess relationships between pelvic floor dysfunction and risk factors and demographic data. A p-value less than 0.05 will be considered statistically significant.
our criteria consists of
Inclusion Criteria:
- Their age will range from 16 to 60 years.
- Female gender only.
- Females engaged in regular sports or athletic activities..
- Currently residing in Egypt
Exclusion Criteria:
- Not currently involved in sports or physical activities.
- Egyptian females living outside Egypt.
- Participants involved in para-athletics. the concent from the participants is taken either verbally or Via the google form sent as mentioned above there will be a consent declaration at the beginning of the form for the participants to approve to participate.
as for the participant withdrawl : A thorough description of the procedure will be explained and they understand they may withdraw their consent and discontinue participation in this research and no consequences for the participant in withdrawing. Their data will be removed.
Study Type
Enrollment (Estimated)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Their age will range from 16 to 60 years.
- Female gender only.
- Females engaged in regular sports or athletic activities..
- Currently residing in Egypt
Exclusion Criteria:
- Not currently involved in sports or physical activities.
- Egyptian females living outside Egypt.
- Participants involved in para-athletics.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
pelvic floor disability index
Time Frame: 2 months
|
the pelvic floor disability index will be used to evaluate pelvic floor.
The questionnaire, transferred to Google Form, consists of 20 questions divided into three sections: Pelvic Organ prolapse Distress Inventory 6 (POPDI-6), Colorectal-Anal distress Inventory 8 (CRAD-8) and Urinary distress Inventory 6 (UDI-6).
|
2 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- P.T.REC/012/005380
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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