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

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ClinicalTrials.gov IDNCT07847294

PhaseNA

Enrollment42

SponsorAnkara Medipol University

Age18 Years – 74 Years

SexALL

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Conditions studied

Diabete Type 2, Diabetes in Adults

About this study

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

Interventions

Behavioral: 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)

Primary outcomes

Canadian Occupational Performance Measure (COPM) (Baseline (Week 0) and Post-intervention (Week 4))
Diabetes Self-Management Questionnaire (DSMQ) (Baseline (Week 0) and Post-intervention (Week 4))
Occupational Balance Questionnaire (OBQ11) (Baseline (Week 0) and Post-intervention (Week 4))
Diabetes Symptom Checklist-Revised (DSC-R) (Baseline (Week 0) and Post-intervention (Week 4))
Short Form-36 Health Survey (SF-36) (Baseline (Week 0) and Post-intervention (Week 4))

Eligibility information

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

Study locations

Ankara Medipol University, Ankara, Turkey (Türkiye)
Ankara Medipol University, Ankara, Turkey (Türkiye)

Before you participate: Varda Clinical is an independent discovery tool, not the study sponsor or a medical provider. Eligibility can only be determined by the official study team. Discuss potential risks and benefits with a qualified healthcare professional.

Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-11-09.