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The Impact of a Mobile Application-based Support and Counseling Program on Women's Knowledge, Attitudes and Self-efficacy in the Preconceptional Period

NCT07279857 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 110

Last updated 2025-12-12

No results posted yet for this study

Summary

This randomized controlled trial aims to evaluate the effect of a mobile application-based support and counseling program on women in the preconception period. The study includes women aged 18 to 49 who plan to conceive within two years and meet the eligibility criteria. Participants are randomly assigned to an intervention group receiving structured preconception counseling through a mobile application or a control group receiving standard information via a booklet. The intervention consists of weekly educational modules delivered over four weeks, followed by follow-up assessments at 4 and 12 weeks. Primary outcomes include changes in preconception knowledge, attitudes, and self-efficacy. The study seeks to determine whether mobile health-based counseling enhances preconception preparedness compared with standard information.

Conditions

  • Preconception Period

Interventions

BEHAVIORAL

Mobile Application-Based Preconception Counseling Program

A structured digital education and counseling program delivered through a mobile application, including weekly modules, reminders, and in-app messaging support.

BEHAVIORAL

Standard Preconception Information Booklet

A printed booklet providing standard guideline-based preconception information without digital follow-up.

Sponsors & Collaborators

  • Selinay Aktaş Demir

    lead OTHER

Principal Investigators

  • Selinay Aktaş Demir, RN, PhD Student · Atlas Üniversitesi

  • Ümran Oskay, PhD, Prof. · Istanbul University - Cerrahpasa

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
49 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-01-01
Primary Completion
2026-09-01
Completion
2026-12-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07279857 on ClinicalTrials.gov