Effects of Family Planning Education Given to Illiterate Women Via Visual Material Support

January 1, 2025 updated by: ESRA GUNEY, PhD, Inonu University

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

Completed

Conditions

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

Interventional

Enrollment (Actual)

74

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

      • Malatya, Turkey
        • Inonu University

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

Accepts Healthy Volunteers

Yes

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

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: 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.
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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Esra Güney, Inonu University

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.

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 31, 2023

Primary Completion (Actual)

May 31, 2023

Study Completion (Actual)

July 31, 2023

Study Registration Dates

First Submitted

December 24, 2024

First Submitted That Met QC Criteria

December 24, 2024

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 1, 2025

Last Verified

January 1, 2025

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)?

NO

IPD Plan Description

Research results will be shared

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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