- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06578364
Effect of Educational Program About Preconception Care on Knowledge and Attitude of Adolescents University Students
September 13, 2024 updated by: Amira Hussin Hussin Mohammed, Delta University for Science and Technology
This quasi-experimental study used a pre-test-post-test design to assess the effectiveness of the teaching program.
A sample of 400 students from El Mansoura University was selected using a simple random sample.
The participants were given a pre-test questionnaire to evaluate their knowledge and attitude towards PCC.
The educational program consisted of a single session, which included a lecture, pictures, videos, and discussions.
The post-test was administered immediately after the program
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
400
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Gamasa, Egypt, 35712
- Amira Hussin Mohammed
-
-
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
Yes
Description
Inclusion Criteria:
- The study included males and females from the targeted colleges.
- Students from grade 1 to grade 4.
- Students who accepted to participate in the study.
Exclusion Criteria:
- Students from the medical sector.
- Students who refused to participate were excluded from 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
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Educational Program about Preconception Care
|
The educational program consisted of a single session, which included a lecture, pictures, videos, and discussions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
knowledge and attitude towards Preconception care (PCC)
Time Frame: The educational program consisted of a single session, which included a lecture, pictures, videos, and discussions. The post-test was administered immediately after the program.
|
The questionnaire includes sections on socio-demographic factors, obstetrics, family planning, and disease-related factors, as well as sections for knowledge and attitude questions
|
The educational program consisted of a single session, which included a lecture, pictures, videos, and discussions. The post-test was administered immediately after the program.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Actual)
January 1, 2023
Primary Completion (Actual)
June 30, 2024
Study Completion (Actual)
June 30, 2024
Study Registration Dates
First Submitted
August 26, 2024
First Submitted That Met QC Criteria
August 27, 2024
First Posted (Actual)
August 29, 2024
Study Record Updates
Last Update Posted (Estimated)
September 19, 2024
Last Update Submitted That Met QC Criteria
September 13, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- Preconception Care
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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