- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06808542
Pelvic Floor Dysfunction Among Female Physiotherapy Students: A Cross-Sectional Study
This study aims to:
- estimate the prevalence of pelvic floor dysfunction among female physiotherapy students at Cairo University.
- identify potential risk factors that may be associated with pelvic floor dysfunction in this student population.
- assess the level of awareness regarding pelvic floor health among female physiotherapy students at Cairo University.
- explore how female physiotherapy students at Cairo University utilize available healthcare resources for managing pelvic floor-related concerns.
Study Overview
Detailed Description
Pelvic floor dysfunction (PFD) is a global health problem that affects millions of women worldwide. It encompasses a broad range of interrelated disorders affecting the pelvic region, including urinary incontinence, pelvic pain, constipation, sexual dysfunction, and pelvic organ prolapse. While PFD is often associated with pregnancy, childbirth, and aging, recent studies suggest that these conditions may also affect younger populations, including nulliparous women.
Pelvic floor health is crucial for supporting pelvic organs, maintaining continence, and facilitating sexual function. However, the impact of PFD on women's health and quality of life is significant, with important consequences for physical and mental well-being. These disorders often coexist and compound each other's impact, leading to disabling symptoms, embarrassment, social isolation, impaired task performance, loss of personal and intimate relationships, and reduced participation in leisure activities.
Despite the substantial burden of PFD, there is a lack of comprehensive data on the prevalence, risk factors, and awareness levels of these conditions among specific populations, particularly young women pursuing higher education. Physiotherapy students, who are expected to have a good understanding of musculoskeletal and pelvic health, represent an important group to study in this context.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Doaa A. Osman, PhD
- Phone Number: 01115792245
- Email: Doaa.osman@cu.edu.eg
Study Contact Backup
- Name: Amira Nagy Abdellatif Hamad, PhD
Study Locations
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-
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Giza, Egypt
- Recruiting
- Cairo University
-
Contact:
- Doaa A. Osman, PhD
- Phone Number: 01115792245
- Email: Doaa.osman@cu.edu.eg
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Principal Investigator:
- Amira Nagy Abdellatif Hamad, PhD
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Principal Investigator:
- Azza Mohamed Abd El-Mohsen, PhD
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Sub-Investigator:
- Arwa Nady Abd El Ghafar Ibrahim, Student
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Sub-Investigator:
- Doha Yousry Ibrahim Mohamed, Student
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Sub-Investigator:
- Farida Khaled Foad Ibrahim, Student
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Virgin undergraduate physiotherapy students.
- Their age will range from 18-25 years.
Exclusion Criteria:
- Neurological disorders or injuries that may affect pelvic floor function (e.g., fibromyalgia and multiple sclerosis).
- Mental health or cognitive disorders that could affect data collection.
- Females who have undergone any form of abdominal surgery prior to the time of the study.
- Females with current use of medications that may affect pelvic floor function (e.g., anticholinergics, opioids, antidepressants).
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Modified Australian pelvic floor questionnaire
Time Frame: 2 months
|
It will be used to estimate the prevalence of pelvic floor disorders through assessing their bladder function, bowel function, and pelvic organ prolapse.
This questionnaire will be administered electronically via online survey platforms.
|
2 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
A self-administered survey
Time Frame: 2 months
|
A self-administered survey will be used to assess potential associated risk factors, including lifestyle habits, weight, BMI, family history, mental health factors (stress, anxiety, depression), physical health factors (sleep, exercise, dietary habits).
Also, it will assess students' awareness of pelvic floor health and their utilization of available healthcare resources for managing pelvic floor-related concerns.
|
2 months
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Doaa A. Osman, PhD, Assistant Professor, Cairo university
Study record dates
Study Major Dates
Study Start (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/005385
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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