NCT07307430Not yet recruiting
Effect of Narrative Education on Glycemic Control in Adults With Type 2 Diabetes in Primary Care
Effect of a Structured Narrative Education Program on Glycemic Control in Adults With Type 2 Diabetes in Primary Care: A Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 31 Dec 2025
Brief summary (registry, in English)
Type 2 diabetes is common in primary care, and daily self-care behaviors are essential for achieving blood sugar targets. This randomized, two-arm clinical trial will evaluate whether a structured narrative education program added to usual diabetes care improves glycemic control compared with usual care alone in adults with type 2 diabetes. Eligible participants (age ≥18 years) with suboptimal glycemic control (HbA1c ≥7.0% in the last 3 months) will be randomized 1:1 to either standard care or standard care plus narrative education. The narrative education program will be delivered by a family physician over 3 months and includes two individual face-to-face sessions (approximately 20-30 minutes) at Day 0 and Day 15 and four brief telephone reinforcement calls (approximately 3-5 minutes) on Days 30, 45, 60, and 75. The primary outcome is the absolute change in HbA1c from baseline (Day 0) to Day 90. Secondary outcomes include changes in diabetes self-care activities (SDSCA-TR), diabetes-related distress (PAID-5-TR), and body mass index (BMI) from Day 0 to Day 90.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 226 (estimated)
- First submitted
- 13 Dec 2025
- Start date
- 15 Feb 2026
- Primary completion date
- 15 Nov 2026
- Lead sponsor
- Mustafa Kemal University
- Diseases
- Type 2 diabetes
- NCT number
- NCT07307430
What you commit to
- Study type: Interventional
- Planned participants: 226
- From 15 Feb 2026 to the primary completion date, 15 Nov 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Major surgery or blood transfusion within the last 3 months
Other illness
- Type 1 diabetes, gestational diabetes, or secondary diabetes
- Acute infection or hospitalization within the last 2 weeks
- Active malignancy or current systemic steroid/immunosuppressive therapy
- Significant cognitive impairment preventing participation
- Current participation in another structured diabetes education program
Who the study is looking for
- Age ≥ 18 years
- Diagnosis of type 2 diabetes mellitus for at least 1 year
- HbA1c ≥ 7.0% measured within the last 3 months prior to enrollment
- Followed in the study family health center and reachable by telephone
- Able to read and write (or able to complete questionnaires with investigator assistance)
- Provides written informed consent
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Ozerli Family Health Center No. 4 Coordinator of this site? Confirm its status | Antakya | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.