Ireland
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Recruiting Not applicable

The Effectiveness of an Occupation-Based Lifestyle Program in Individuals With Type 2 Diabetes

NCT07847294 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-09-01
Last updated
2026-09-29

Condition(s) studied

Diabete Type 2Diabetes in Adults

Investigational drug(s) / intervention(s)

Occupation-Based Lifestyle Program

Occupation-Based Lifestyle Program: An online, 5-module (8 sessions, 60 minutes each, twice weekly via Zoom) intervention led by occupational therapy staff. The program incorporates diabetes awareness, structured problem-solving, stress management (mindfulness), energy conservation, safe physical activity integration, and goal setting using the Canadian Occupational Performance Measure (COPM)

Study summary

This study aims to investigate the effect of an occupation-focused lifestyle program on occupational performance, self-management, occupational balance, diabetes symptoms, and quality of life in individuals with Type 2 diabetes.

Type 2 diabetes requires continuous daily management, yet conventional interventions often show limited long-term behavioral sustainability. Occupation-focused lifestyle interventions offer a holistic approach by addressing daily routines, self-management skills, and personal goals.

In this non-invasive, quasi-experimental study, participants aged 18-74 with Type 2 diabetes will be invited via social media announcements. Participants will be divided into an intervention group and a control group. The intervention group will receive an online, 5-module (8 sessions) Occupation-Focused Lifestyle Program via Zoom, covering diabetes awareness, problem-solving, stress management (mindfulness), energy conservation/physical activity, and goal review. The control group will receive an informative brochure after the intervention group completes the program. Outcomes will be measured online before and after the program using structured scales to evaluate changes in daily functioning, self-care, and overall well-being

Eligibility

Sex
ALL
Min age
18 Years
Max age
74 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosed with Type 2 Diabetes Mellitus for at least 12 months * Aged between 18 and 74 years * Ability to provide documented proof of Type 2 diabetes diagnosis (e.g., medical report or official documentation) * Having access to a smartphone, tablet, or computer with an internet connection to attend online Zoom sessions and complete online questionnaires -Voluntary agreement to participate in the study and submission of an online informed consent form Exclusion Criteria: * Presence of severe diabetic complications that significantly impair independent daily function (e.g., severe proliferative retinopathy, end-stage renal disease, active foot ulcers, or severe diabetic neuropathy) * Cognitive impairment, acute psychiatric conditions, or sensory deficits (uncorrected visual or hearing impairments) that impede active participation in group sessions or online communication * Participation in another structured diabetes self-management program or lifestyle intervention trial simultaneously

Primary outcome measure(s)

  • Canadian Occupational Performance Measure (COPM) — Baseline (Week 0) and Post-intervention (Week 4)
    Assesses individual occupational performance and satisfaction in self-care, productivity, and leisure domains. Scores range from 1 to 10 for both subscales, with higher scores indicating higher self-perceived performance and satisfaction.
  • Diabetes Self-Management Questionnaire (DSMQ) — Baseline (Week 0) and Post-intervention (Week 4)
    Evaluates self-care behaviors related to glycemic control, where higher scores indicate better self-management practices.
  • Occupational Balance Questionnaire (OBQ11) — Baseline (Week 0) and Post-intervention (Week 4)
    Measures satisfaction with the balance of daily activities and roles, with higher scores reflecting greater occupational balance.
  • Diabetes Symptom Checklist-Revised (DSC-R) — Baseline (Week 0) and Post-intervention (Week 4)
    Evaluates the presence and perceived burden of diabetes-related physical and psychological symptoms.
  • Short Form-36 Health Survey (SF-36) — Baseline (Week 0) and Post-intervention (Week 4)
    Measures health-related quality of life across physical and mental health domains, with higher scores reflecting better health status.

Trial sites (2)

FacilityCityRegionStatus
Ankara Medipol University Ankara Turkey (Türkiye) Recruiting
Ankara Medipol University Ankara Turkey (Türkiye) Recruiting
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 NCT07847294 on ClinicalTrials.gov ↗ ← All trials in Turkey