NCT06632171Completed
CBT-based and Motivational Interviewing Supported Psychoeducation in Obese Individuals
The Effect of Cognitive Behavioral Therapy-Based and Motivational Interviewing-Supported Psychoeducation on Emotional Eating and Psychological Resilience in Individuals With Obesity
Source: ClinicalTrials.gov · Last updated 4 Nov 2026
Brief summary (registry, in English)
The aim of this study was to examine the effects of cognitive-behavioral and motivational interviewing-supported psychoeducation on emotional eating and psychological resilience in individuals with obesity. The study was conducted using a randomized controlled experimental design. The initial planned sample size was 102 individuals, with 51 participants allocated to each group. However, due to difficulties in participant recruitment, a subsequent power analysis was conducted, which indicated a minimum total sample size of 32 participants. Ultimately, 84 individuals who met the inclusion criteria were randomized into the experimental (n = 42) and control (n = 42) groups, and 81 participants completed the study (experimental: n = 40; control: n = 41). A cognitive-behavioral and motivational interviewing-supported psychoeducation program was applied to the experimental group. Participants were evaluated at three time points: pre-test (baseline), post-test (8 weeks), and follow-up test (2 months after the post-test). No intervention was applied to the control group. The Emotional Eating Scale and Psychological Resilience Scale were used as data collection tools in the study. The study tested the hypothesis that the cognitive-behavioral and motivational interviewing-supported psychoeducation program would be effective in reducing emotional eating levels and increasing psychological resilience in individuals with obesity. The findings of the study may contribute to understanding the potential importance of psychological approaches in the treatment of obesity.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 84 (actual)
- First submitted
- 6 Oct 2024
- Start date
- 25 Nov 2024
- Primary completion date
- 5 Aug 2025
- Lead sponsor
- Inonu University
- Diseases
- Obesity
- NCT number
- NCT06632171
What you commit to
- Study type: Interventional
- Participants enrolled: 84
- From 25 Nov 2024 to the primary completion date, 5 Aug 2025
- 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.
Other illness
- Having a medical condition (e.g. Cushing syndrome, hypothyroidism) or taking medication that causes obesity
- Having a psychiatric diagnosis (e.g. depression, anxiety disorder, eating disorder) or taking psychotropic medication
Other
- Having communication problems
- Being pregnant or breastfeeding
- Participating in another diet or exercise program
Who the study is looking for
- Obese individuals (body mass index 30 kg/m2 or more)
- Between the ages of 18-65
- Not having any psychiatric disorder or not using psychiatric medication
- Volunteering to participate in psychoeducation
- Being in a physical and mental condition that will allow them to adapt to treatment
- Signing the informed consent form
Age in the registry: 18 years to 65 years · 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 |
|---|---|---|---|
| Muş State Hospital and Muş Central Healthy Life Center Coordinator of this site? Confirm its status | Muş | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.