Investigation of the Effect of Sexuality-Based Family Planning Education Given to Women Via Podcast on Contraceptive Method Selection and Sexual Life Quality

March 19, 2024 updated by: Zeynep Dilşah Karaçam Yılmaz, Marmara University

In this study, it was aimed to examine the effect of Sexuality-Based Family Planning Education given to women of childbearing age via Podcast on contraceptive method selection and sexual life quality.

Accordingly, the hypotheses of the study are as follows:

Hypotheses of the Project H1: Sexuality-based family planning education via podcast has an effect on women's conscious and appropriate contraceptive method selection.

H2: Sexuality-based family planning education via podcast has a positive effect on women's sexual life quality.

H3: Sexuality-based family planning education via podcast has a positive effect on the quality of sexual life of women by increasing their level of contraceptive knowledge.

H4: Sexuality-based family planning education via podcast has a positive effect on women's attitudes towards family planning.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

The aim of this study was to examine the effect of sexuality-based family planning education given to women of childbearing age via podcast on contraceptive method selection and sexual life quality.

The study is planned to be conducted as a randomized controlled experimental study and women of childbearing age within the borders of Istanbul will be included in the study. The research will be conducted between November 2023 and May 2024 and a total of 176 women will be included in the study. The included women will be divided into two groups as experimental and control groups. Data will be collected by applying the Personal Information Form, Contraceptive Knowledge Rating Scale-Turkish Form (CKRA-TR), Sexual Quality of Life Scale-Woman (SQLS-W) and Family Planning Attitude Scale (FPAS). Women in the experimental group will be given sexuality-based family planning education consisting of 5 modules via podcasts. In addition, a brochure on family planning and education will be shared with the women in the experimental and control groups. The data obtained in the research will be entered into the database in IBM SPSS 29.0 (Statistical Package for the Social Sciences) program and all necessary statistical analyzes will be performed in the same program.

Study Type

Interventional

Enrollment (Estimated)

176

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

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:

  • Volunteer to participate in the study,
  • 15-49 years old,
  • Does not have any physical or mental disability,
  • At least primary school education,
  • At least one sexual partner,
  • Sexually active women will be included in the study.

Exclusion Criteria:

  • Not sexually active in the last 4 weeks,
  • Trained in the use of contraceptive methods,
  • Being treated for any sexual dysfunction,
  • Women with any psychiatric illness will be 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: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control group
Control
Experimental: Experimental group
Sexuality-based family planning education will be provided through podcasts.
Behavioral: Sexuality-Based Family Planning Education via Podcast
The training program is planned to consist of 5 modules. These trainings will be shared module by module on a daily basis through an application (Spotify) where podcasts are shared. These modules are as follows: 1. Sexual and Reproductive Health / Sexual Rights / Female-Male / Physiology of Sexual Functions, 2. Sexual Myths, 3. Contraceptive Methods-1, 4. Contraceptive Methods-2, 5. Sexually Transmitted Diseases / Safe Sexual Intercourse As a result of randomization, the links of the podcasts will be shared with the women in the experimental group one by one on a daily basis. Podcasts are planned to last an average of 10 minutes. This training content is planned for 5 days and the second tests will be applied by the researcher to the women who finish the podcasts. The 3rd tests will be applied 4 weeks after the second tests.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Contraceptive Knowledge Assessment Scale-Turkish Form
Time Frame: Through study completion, an average of 6 months
It will be used to measure contraception knowledge levels.
Through study completion, an average of 6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Sexual Quality of Life Scale-Female
Time Frame: Through study completion, an average of 6 months
It will be used to measure quality of life.
Through study completion, an average of 6 months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Family Planning Attitudes Scale
Time Frame: Through study completion, an average of 6 months
It will be used for the measurement of family planning attitudes.
Through study completion, an average of 6 months

Collaborators and Investigators

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

Sponsor

Marmara 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.

General Publications

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)

February 9, 2024

Primary Completion (Estimated)

June 10, 2024

Study Completion (Estimated)

August 10, 2024

Study Registration Dates

First Submitted

March 12, 2024

First Submitted That Met QC Criteria

March 19, 2024

First Posted (Actual)

March 26, 2024

Study Record Updates

Last Update Posted (Actual)

March 26, 2024

Last Update Submitted That Met QC Criteria

March 19, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • MU-Ebe-ZDKY-02

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

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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