- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07544316
Investigating the Barriers and Possibilities for Improving the Healthcare Service of Female Survivors of Gender-based Violence in Upper Egypt
Barriers and Opportunities in Delivering Healthcare Services for Survivors of Gender-Based Violence: Experience From a Safe Women's Unit in Upper Egypt
Study Overview
Status
Conditions
Detailed Description
Gender-based violence (GBV) constitutes a major public health and human rights issue worldwide, defined as physical, psychological, sexual, or economic acts that cause harm based on gender. GBV disproportionately affects women. An estimated 35% of women globally have experienced domestic or sexual abuse in their lifetime, with female survivors experiencing higher rates of injury and long-term physical and mental health sequelae compared to men. Healthcare providers are uniquely positioned to identify, manage, and refer affected women, as many survivors seek care within hospital settings.
The OB-GYN department serves as a critical entry point for survivors seeking reproductive health services, antenatal care, and emergency obstetric interventions, often representing the first opportunity for intervention. Violence during pregnancy is associated with adverse maternal and fetal outcomes, underscoring the need for survivor-centered services in Egypt. Since 2019, UNFPA, the National Council for Women, and the Egyptian Ministry of Health and Population have established 33 Safe Women Clinics across Egypt, providing multidisciplinary care, though barriers such as limited training, resources, stigma, and inadequate coordination persist. The 2022 launch of the Arabic Protocol on Healthcare for Women Subjected to Gender-Based Violence strengthened provider response by establishing standardized guidance on clinical management, screening, and referral.
Given that survivors utilize health services more frequently than any other form of assistance, health professionals are uniquely positioned to recognize and respond to abuse; however, they often inadequately address such cases. This study presents data and professional recommendations on identifying and managing GBV in clinical settings, with attention to the needs of Indigenous women exposed to violence or abuse.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Tarek A Hussein, MBChB
- Phone Number: +201013888833
- Email: Tarek.16266338@med.aun.edu.eg
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Healthcare providers
- Female survivors of Violence
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Identification of key barriers affecting healthcare service delivery for women survivors of gender-based violence.
Time Frame: Within 1 year
|
Within 1 year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Development of recommendations to improve Women's Safe Units in Egypt.
Time Frame: Within 1 year
|
Within 1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Tarek A Hussein, MBChB, Assiut University
- Study Chair: Kamal M Zahran, Professor, Assiut University
- Study Director: Sherif M Badran, Lecturer, Assiut University
- Study Director: Abdulrahman M Rageh, Lecturer, Assiut University
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
Keywords
Other Study ID Numbers
- Gender-Based Violence(GBV)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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