- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06755749
Effects of Family Planning Education Given to Illiterate Women Via Visual Material Support
Effects of Family Planning (FP) Education Given to Married Illiterate Women of Reproductive Age Via Visual Material Support on FP-Related Attitudes and Contraceptive Preferences: the Case of Viranşehir
This study was conducted to determine the effects of family planning education given to married illiterate women of reproductive age via visual material support on their family planning attitudes and contraceptive preferences.in this study, it was aimed to provide education to married illiterate women of reproductive age using visual materials to change their FP-related attitudes in a positive direction and transform these attitudes into positive fertility behaviors.
The hypotheses of the study were as follows:
H1a: FP education given with visual materials increases positive attitudes toward FP in illiterate women.
H1b: FP education given with visual materials affects the contraceptive preferences of illiterate women.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study was conducted to determine the effects of family planning education given to married illiterate women of reproductive age via visual material support on their family planning attitudes and contraceptive preferences.
Method: The randomized controlled study was carried out between 31 January and 31 July 2023. The sample of the study consisted of 148 women, including 74 in the experimental group and 74 in the control group. Using a Family Planning Education Booklet prepared for illiterate women, an education program lasting a week in total was held in three sessions. No intervention was made in the control group. Data were collected using a Personal Information Form, a Family Planning Assessment Form, and the Family Planning Attitude Scale. No intervention was made in the control group. The same data collection instruments were administered to the participants in the control group simultaneously with the experimental group in the pretest (day 1) and posttest (day 7) phases.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Malatya, Turkey
- Inonu University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being able to communicate,
- Not having any visual or auditory problems that could prevent communication,
- Being aged 15-49 and married,
- Not having a diagnosis of chronic illness (e.g., cardiovascular diseases, asthma, epilepsy),
- Not receiving any FP-related education within the last 21 days.
Exclusion Criteria:
- - Being currently pregnant,
- Planning to get pregnant soon,
- Receiving medical treatment for any diagnosed chronic illness.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control Group
No intervention was made in the control group.
|
|
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Experimental: Group receiving Family Planning Education with Visual Material Support
Using a Family Planning Education Booklet prepared for illiterate women, an education program lasting a week in total was held in three sessions.
|
Stage 1 (Day 1, 10-15 min): The education content for Session 1 in the FP Education Booklet prepared by the researchers was provided to the participants using the face-to-face interview method. After making an appointment for Stage 2 (Day 3) to be carried out at the FHC, the first stage of the data collection process was complete. Stage 2 (Day 3, 10-15 min): The education content for Session 2 in the FP Education Booklet was provided to the participants who arrived at the FHC on their predetermined appointment days using the face-to-face interview method. After making an appointment for Stage 3 (Day 7) to be carried out at the FHC, the second stage of the data collection process was complete. Stage 3 (Day 7, 1-5 min): The data collection forms were administered again to the participants who arrived at the FHC on their appointment days assigned at Stage 2, and the data collection process was complete. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Family Planning Attitude
Time Frame: 7 days
|
Its total score range is 34-170, and higher scores indicate more positive attitudes toward FP.
The subscales of the scale are Attitudes of Society toward Family Planning (score range: 15-75), Attitudes of Respondent toward Family Planning (score range: 11-55), and Attitudes of Respondent toward Pregnancy (score range: 8-40).
|
7 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Family Planning Assessment
Time Frame: 7 days
|
The form, which was created by the researchers by reviewing the literature, included questions about the characteristics of the participants such as the contraceptive methods they were currently using, their reasons for using (preferring) the current method, the person (self or spouse) selecting the method, previously used FP methods and reasons for quitting, the person (self or spouse) choosing to quit the method, and whether they were satisfied with the methods they used.
|
7 days
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Esra Güney, Inonu University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Other Study ID Numbers
- 2022/3724
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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