The Effect of Social Media-Based Education on the Knowledge and Attitudes of Women of Childbearing Age in the Preconception Period and on Healthy Lifestyle Behaviors

July 21, 2025 updated by: YASEMİN AYDIN KARTAL, Saglik Bilimleri Universitesi
In order to determine the effect of education provided through social media on the knowledge and attitudes of women of childbearing age during the preconceptional period and its relationship with healthy lifestyle behaviors, a randomized controlled pre-test and post-test design and control group was planned. The research universe will consist of women of childbearing age who applied to Ümraniye Education and Research Hospital, agreed to participate in the study and met the inclusion criteria (N: 80). In this randomized controlled pre-test and post-test design and control group study, in order to determine the sample size; the data were normally distributed, the standard deviation of the main mass was estimated as 1 and the effect size (difference) was estimated as 0.8. For the analysis to be conducted, it was calculated that the highest power value of the study would be 0.942182 if two independent n₁=40, n₂=40 samples were taken at a significance level of 5%. The G-power analysis result is given below. In addition, after the data collection, the adequacy of the sample size in the study will be evaluated with a post hoc power analysis. Women who volunteer to participate in the study will be assigned to the intervention and control groups using a computer-aided simple random sampling method. Computer-aided randomization will be used in the study, and the number of cases will be entered through the program with the URL address https://www.randomizer.org and random assignment will be made to the intervention and control groups. Preconceptional period education will be provided to the women in the intervention group via social media. No application will be made to the control group.

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

80

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 Contact

Study Contact Backup

Study Locations

      • Istanbul, Turkey
        • University of Health Sciences

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
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Being willing to participate in the study.
  • Being a woman of childbearing age
  • Planning to get pregnant within 1 year
  • Using Instagram and WhatsApp

Exclusion Criteria:

- Being pregnant

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention group (n:40)
Participants in the intervention group will be required to follow the Instagram account created specifically for the training. The Instagram account will be made private to prevent women in the control group from accessing Instagram posts. The training provided via Instagram will last 2 weeks, including the process of sharing all posts and videos. After the completion of the training, the "Healthy Lifestyle Behaviors Scale" and the "Preconceptional Knowledge and Attitude Scale" will be applied as a post-test.
Participants in the intervention group will be required to follow the Instagram account created specifically for the training. The Instagram account will be made private to prevent women in the control group from accessing Instagram posts. The training provided via Instagram will last 2 weeks, including the process of sharing all posts and videos. After the completion of the training, the "Healthy Lifestyle Behaviors Scale" and the "Preconceptional Knowledge and Attitude Scale" will be applied as a post-test.
No Intervention: Control group (n:40
No application will be made. After all stages of the research are completed, training will be applied to the control group participants. After the research is completed, all participants will be given a brochure containing the information in the training content.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Introductory Information Form
Time Frame: 10 minutes
This form, created by researchers based on literature, includes questions about the participants' age, obstetric history, healthy lifestyle behaviors, etc.
10 minutes
Healthy Lifestyle Behaviors Scale (HLBS-II)
Time Frame: 10 minutes
The scale, whose validity and reliability study was conducted in our country by Bahar et al. in 2008, was developed by Walker et al. in 1996 to measure the health-enhancing behaviors of the individual in relation to a healthy lifestyle. The scale has six sub-dimensions: health responsibility (3,9,15,21,27,33,39,45,51), physical activity (4,10,16,22,28,34,40,46), nutrition (2,8,14,20,26,32,38,44,50), spiritual development (6,12,18,24,30,36,42,48,52), interpersonal relations (1,7,13,19,25,31,37,43,49) and stress management (5,11,17,23,29,35,41,47) and consists of a total of 52 items. The interpersonal relations scale sub-dimension evaluates the relationships between the individual and the environment. Communication is necessary in a healthy relationship.
10 minutes
Preconceptional Knowledge and Attitude Scale
Time Frame: 10 minutes
It was developed by Gökdemir and Eryılmaz in 2022. The original language of the scale is Turkish and it is a 5-point Likert type. The scale can be applied to married and single women between the ages of 18-45 who are of childbearing age. The Preconceptional Knowledge and Attitude Scale consists of a total of 43 items, 42 positive (straight) and 1 negative (reverse) item, and 7 sub-dimensions (factors). The distribution of the items in the scale to the factors is as follows. Factor 1 (Attitudes Towards Preconceptional Health Protection and Development): There are a total of 10 items in this dimension, consisting of items 10, 15, 17, 18, 19, 21, 23, 25, 26, and 31. Factor 2 (Attitudes Towards Fertility Planning): This dimension consists of items 28, 30, 32, 34, 38, 39, and 40, and has a total of 7 items. Factor 3 (Attitudes Towards Living Conditions Before Having Children): This dimension consists of items 27, 29, 41, 35, and 42, and has a total of 5 items.
10 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Introductory Information Form
Time Frame: 10 minutes
This form, created by researchers based on literature, includes questions about the participants' age, obstetric history, healthy lifestyle behaviors, etc.
10 minutes
Healthy Lifestyle Behaviors Scale (HLBS-II)
Time Frame: 10 minutes
The scale, whose validity and reliability study was conducted in our country by Bahar et al. in 2008, was developed by Walker et al. in 1996 to measure the health-enhancing behaviors of the individual in relation to a healthy lifestyle. The scale has six sub-dimensions: health responsibility (3,9,15,21,27,33,39,45,51), physical activity (4,10,16,22,28,34,40,46), nutrition (2,8,14,20,26,32,38,44,50), spiritual development (6,12,18,24,30,36,42,48,52), interpersonal relations (1,7,13,19,25,31,37,43,49) and stress management (5,11,17,23,29,35,41,47) and consists of a total of 52 items. The interpersonal relations scale sub-dimension evaluates the relationships between the individual and the environment. Communication is necessary in a healthy relationship.
10 minutes
Preconceptional Knowledge and Attitude Scale
Time Frame: 10 minutes
It was developed by Gökdemir and Eryılmaz in 2022. The original language of the scale is Turkish and it is a 5-point Likert type. The scale can be applied to married and single women between the ages of 18-45 who are of childbearing age. The Preconceptional Knowledge and Attitude Scale consists of a total of 43 items, 42 positive (straight) and 1 negative (reverse) item, and 7 sub-dimensions (factors). The distribution of the items in the scale to the factors is as follows. Factor 1 (Attitudes Towards Preconceptional Health Protection and Development): There are a total of 10 items in this dimension, consisting of items 10, 15, 17, 18, 19, 21, 23, 25, 26, and 31. Factor 2 (Attitudes Towards Fertility Planning): This dimension consists of items 28, 30, 32, 34, 38, 39, and 40, and has a total of 7 items. Factor 3 (Attitudes Towards Living Conditions Before Having Children): This dimension consists of items 27, 29, 41, 35, and 42, and has a total of 5 items.
10 minutes

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 (Estimated)

October 5, 2025

Primary Completion (Estimated)

December 5, 2025

Study Completion (Estimated)

February 5, 2026

Study Registration Dates

First Submitted

December 7, 2024

First Submitted That Met QC Criteria

July 21, 2025

First Posted (Actual)

July 24, 2025

Study Record Updates

Last Update Posted (Actual)

July 24, 2025

Last Update Submitted That Met QC Criteria

July 21, 2025

Last Verified

July 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • SBU-AYDINKARTAL-012

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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