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Clinical Trials in Turkey / NCT07318740
Active, not recruiting Not applicable

Effectiveness of Mobile Application-Supported Education and Counseling in Pregnant Women With Gestational Diabetes

NCT07318740 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-08-18
Last updated
2026-01-06

Condition(s) studied

Gestational Diabetes Mellitus (GDM)

Investigational drug(s) / intervention(s)

Mobile Application-Based Education and Counseling ProgramStandard Face-to-Face Gestational Diabetes Education

Mobile Application-Based Education and Counseling Program: A two-week structured education and counseling program delivered via the SugarMoms mobile application for gestational diabetes management. Education is provided by a certified diabetes nurse educator and includes topics such as gestational diabetes management, blood glucose monitoring, insulin therapy, management of hypo/hyperglycemia, healthy nutrition, physical activity, and pregnancy health recommendations. Each module includes audio support, a question-and-answer component, and daily motivational notifications. Participants will log daily blood glucose, dietary intake, and physical activity in the app and continue app use throughout the study. Follow-up assessments and questionnaires are delivered through the app, and progress is monitored via the administrator panel.

Standard Face-to-Face Gestational Diabetes Education: A two-week standard face-to-face gestational diabetes education program provided by a certified diabetes nurse educator in accordance with hospital protocol. The program covers the same topics as the intervention group's app-based program. Blood glucose monitoring is recorded using paper-based forms.

Study summary

This randomized controlled trial aims to evaluate the impact of mobile application-supported education and counseling on the intention, attitude, behavior, and self-efficacy of pregnant women diagnosed with gestational diabetes. The study will be conducted at Ankara Bilkent City Hospital, with participants assigned to intervention and control groups. The intervention group will receive planned education and counseling via a mobile application, while the control group will receive standard hospital education. Data will be collected at predetermined intervals, and outcomes will be compared between the groups. The study seeks to determine the effectiveness of a mobile application-supported approach in the management of gestational diabetes.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
45 Years
Healthy volunteers
No
Inclusion Criteria: Pregnant women aged ≥18 years. Minimum education level: primary school graduate. Singleton pregnancy. No prior diagnosis of gestational diabetes mellitus (GDM). Newly diagnosed with GDM based on oral glucose tolerance test (OGTT) results. Currently receiving insulin treatment as part of the clinical management plan. Absence of comorbid conditions such as hypertension, preeclampsia, or other chronic diseases. Ability to read and understand Turkish. Ownership of a smartphone (iOS/Android) with internet access. Willingness to participate and provide written informed consent. Exclusion Criteria: Development of pregnancy-related complications during the follow-up period. Incomplete or missing data in the study forms. Non-compliance with study protocol. Withdrawal from the study at the participant's request.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ankara Bilkent City Hospital Ankara Turkey (Türkiye)

More Saglik Bilimleri Universitesi trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07318740 on ClinicalTrials.gov ↗ ← All trials in Turkey