- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05846048
Marital Rape:Knowledge, Attitudes and Prevalence in Asample of Married Women in Sohag Governorate
January 6, 2024 updated by: Alaa Mohamed Mahmoud, Sohag University
this study aims at estimation of prevalence of marital rape attitudes and knowledge towards it using semi structured questionnaire
Study Overview
Status
Not yet recruiting
Intervention / Treatment
Detailed Description
this study trying to estimate knowledge of married women in sohag about marital rape attitudes towards it the size of the problem psychological , mental ,physical health consequences if the problem deserve criminalization
Study Type
Observational
Enrollment (Estimated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Alaa M Mazen, demonstrator
- Phone Number: 01016516767
- Email: alaamazen@med.sohag.edu.eg
Study Contact Backup
- Name: soheir A Mohamed, professor
Study Locations
-
-
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Sohag, Egypt
- Sohag University Hospital
-
Contact:
- Magdy M Amin, professor
-
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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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
married females in sohag governorate
Description
Inclusion Criteria:
- married or previously married females
Exclusion Criteria:
- mentally disabled or who with low IQ
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
attitudes to marital rape questionnaire
Time Frame: 6 months
|
married waomen know about marital rape or not
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
prevalence of marital rape questionnaire
Time Frame: 6 months
|
size of the proplem
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Basile KC. Prevalence of wife rape and other intimate partner sexual coercion in a nationally representative sample of women. Violence Vict. 2002 Oct;17(5):511-24. doi: 10.1891/vivi.17.5.511.33717.
- Bergen RK, Bukovec P. Men and intimate partner rape: characteristics of men who sexually abuse their partner. J Interpers Violence. 2006 Oct;21(10):1375-84. doi: 10.1177/0886260506291652.
- Jackson AL. State contexts and the criminalization of marital rape across the United States. Soc Sci Res. 2015 May;51:290-306. doi: 10.1016/j.ssresearch.2014.10.001. Epub 2014 Oct 14.
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 (Estimated)
February 1, 2024
Primary Completion (Estimated)
April 1, 2024
Study Completion (Estimated)
June 30, 2024
Study Registration Dates
First Submitted
April 26, 2023
First Submitted That Met QC Criteria
May 4, 2023
First Posted (Actual)
May 6, 2023
Study Record Updates
Last Update Posted (Actual)
January 9, 2024
Last Update Submitted That Met QC Criteria
January 6, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- Soh-Med-23-11-03MS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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