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
1 other identifier
interventional
81
1 country
1
Brief Summary
The aim of this study is to examine the effects of cognitive-behavioral and motivational interview-supported psychoeducation on emotional eating and psychological resilience in obese individuals. The study will be conducted with a randomized controlled experimental design. The sample of the study will consist of 102 obese individuals in total, 51 in the experimental group and 51 in the control group, who meet the inclusion criteria. A cognitive-behavioral and motivational interview-supported psychoeducation program will be applied to the experimental group. All patients will be evaluated at three time points: pre-test (baseline), post-test (8 weeks), and follow-up test (3 months after the post-test). No intervention will be applied to the control group. The Emotional Eating Scale and Psychological Resilience Scale will be used as data collection tools in the study. As a result of the study, the hypothesis that the cognitive-behavioral and motivational interview-supported psychoeducation program is effective in reducing the emotional eating levels of obese individuals and increasing their psychological resilience levels will be tested. The findings of the study will contribute to the importance and effectiveness of psychological approaches in the treatment of obesity.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable obesity
Started Nov 2024
Shorter than P25 for not_applicable obesity
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 6, 2024
CompletedFirst Posted
Study publicly available on registry
October 8, 2024
CompletedStudy Start
First participant enrolled
November 25, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 5, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
August 5, 2025
CompletedMarch 3, 2026
February 1, 2026
6 months
October 6, 2024
February 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Emotional Eating Scale
Emotional eating was assessed using the Emotional Eating Scale (EES). Scores range from 0 to 30; higher scores indicate a worse outcome (greater emotional eating).
Baseline; end of week 8 (post-intervention); 2-month follow-up
Resilience scale
Resilience was assessed using a resilience scale. Scores range from 0 to 84; higher scores indicate greater resilience (better outcome).
Baseline; post-intervention (end of week 8); 2-month follow-up
Study Arms (2)
Psychoeducation Group
EXPERIMENTALObese individuals in this group receive the structured cognitive behavioral therapy-based and motivational interviewing-supported psychoeducation program.
Control Group
NO INTERVENTIONObese individuals in this group did not receive any interventional procedure during the study period. Only assessment measurements were conducted for research purposes. After completion of follow-up assessments, the psychoeducation program was offered to those who requested it.
Interventions
An 8-week structured psychoeducation program based on cognitive behavioral therapy principles and supported by motivational interviewing techniques.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- Having communication problems
- 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
- Being pregnant or breastfeeding
- Participating in another diet or exercise program
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Inonu Universitylead
Study Sites (1)
Muş State Hospital and Muş Central Healthy Life Center
Muş, Muş, 49000, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer
Study Record Dates
First Submitted
October 6, 2024
First Posted
October 8, 2024
Study Start
November 25, 2024
Primary Completion
June 5, 2025
Study Completion
August 5, 2025
Last Updated
March 3, 2026
Record last verified: 2026-02