- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07464067
Family Planning Methods Among Women in Assuit Egypt
March 5, 2026 updated by: Kerols Tarek Fathy, Assiut University
Knowledge, Attitude and Practice of Different Family Planning Methods Among Women in Assiut,Egypt: a Cross Sectional Study
- To assess the knowledge , attitude and practices of different types of family planning method among women of reproductive age group, and their correlation with socidemographic and socioeconomic factors .
- To identify the reasons which withhold the practices of contraceptive methods .
- To provide baseline information that may help in improving family planning education and counseling services.
Study Overview
Status
Not yet recruiting
Conditions
Detailed Description
Family planning is a key aspect of reproductive health that enables individuals and couples to decide freely on the number and spacing of their children.
Effective use of contraceptive methods helps prevent unintended pregnancies and supports maternal and child well-being .
Despite its importance, many women lack sufficient knowledge about the variety of contraceptive options available.
Limited awareness about how to use these methods correctly can reduce their effectiveness and lead to irregular or incorrect use.
Socioeconomic and reproductive factors play a crucial role in shaping women's use of family planning, as elements such as educational level, income, occupation, age at marriage, source of information, number of pregnancies, and number of living children can all influence both attitudes and practical use of contraceptives .
Access to healthcare services, including counseling and education, is another critical factor affecting the uptake of family planning methods, and women who receive proper guidance are more likely to choose and continue using suitable contraceptives .
Community expectations and family support also impact contraceptive practices, as influence from friends and close social circles can either encourage or discourage women from using family planning methods .
Local assessments in Egypt, including in Assiut, show differences in knowledge and practice among population groups, and understanding these variations is essential for designing effective educational programs and interventions to improve family planning utilization .
Study Type
Observational
Enrollment (Estimated)
350
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: kerols tarek fathy, MBBCh
- Phone Number: +201276590406
- Email: kerotarek049@gmail.com
Study Locations
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Asyut, Egypt
- Assuit University Hospital
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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
- Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
married women between 18 - 49 years
Description
Inclusion Criteria:
- Married women aged between ( 18- 49 ) .
- Attending antenatal care (ANC) at selected health facilities.
- Willing to give informed consent
Exclusion Criteria:
- Women with known psychiatric or cognitive impairments affecting judgment..
- Women outside the reproductive age range (<18 or >49 years).
- Women who refuse to give consent or withdraw during the study
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 |
|---|---|---|
|
-Questionnaire to evaluate the overall knowledge, perceptions, and actual use of family planning methods among married women in the selected areas of Egypt
Time Frame: through study completion, an average of 1 year
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Questionnaire between married women aged 18-49 years
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through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
To explore sociocultural and economic factors that influence the decision to adopt or avoid specific family planning methods.
Time Frame: through study completion, an average of 1 year
|
questionnaire to assess sociocultural and economic factors
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through study completion, an average of 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: ahmed mohamed abo el hasn, MD, Faculty of medicine
- Principal Investigator: Ali Haroun ali, MD, Faculty of medicine
- Principal Investigator: ahmed aboelsoud abden, MD, Faculty of medicine
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.
Helpful Links
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)
June 1, 2026
Primary Completion (Estimated)
June 1, 2027
Study Completion (Estimated)
September 1, 2027
Study Registration Dates
First Submitted
March 2, 2026
First Submitted That Met QC Criteria
March 5, 2026
First Posted (Actual)
March 11, 2026
Study Record Updates
Last Update Posted (Actual)
March 11, 2026
Last Update Submitted That Met QC Criteria
March 5, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- family planning methods
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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