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Not yet recruiting NCT07082140

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

No phase Interventional Social Media Based Education

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Social media based education.
Who it may be relevant to
Registry conditions: Social Media Based Education. Basic parameters: from 18 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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.

Interventions

  • Other Social media based education
    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 a

Primary outcome measures

  • Introductory Information Form [Time frame: 10 minutes]
  • Healthy Lifestyle Behaviors Scale (HLBS-II) [Time frame: 10 minutes]
  • Preconceptional Knowledge and Attitude Scale [Time frame: 10 minutes]
Secondary outcome measures (3)
  • Introductory Information Form [Time frame: 10 minutes]
  • Healthy Lifestyle Behaviors Scale (HLBS-II) [Time frame: 10 minutes]
  • Preconceptional Knowledge and Attitude Scale [Time frame: 10 minutes]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Other

Study locations

Turkey (Türkiye) · 1 center
  • University of Health Sciences — Istanbul

Identifiers

NCT: NCT07082140 · SBU-AYDINKARTAL-012

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗