Skip to main content
OpenTrials
Completed

NCT Number: NCT06632171

CBT-based and Motivational Interviewing Supported Psychoeducation in Obese Individuals

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Muş State Hospital and Muş Central Healthy Life Center

Muş, 49000, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

Cognitive Behavioral Therapy- Based and Motivational Interviewing-Supported Psychoeducation

Behavioral

An 8-week structured psychoeducation program based on cognitive behavioral therapy principles and supported by motivational interviewing techniques.

Primary outcomes

  1. Emotional Eating Scale

    Time frame: Baseline; end of week 8 (post-intervention); 2-month follow-up

    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).

  2. Resilience scale

    Time frame: Baseline; post-intervention (end of week 8); 2-month follow-up

    Resilience was assessed using a resilience scale. Scores range from 0 to 84; higher scores indicate greater resilience (better outcome).

Sponsors and collaborators

Lead sponsor

Inonu University

Other

Registry information

Official study title

The Effect of Cognitive Behavioral Therapy-Based and Motivational Interviewing-Supported Psychoeducation on Emotional Eating and Psychological Resilience in Individuals With Obesity

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Oct 8, 2024
Registry last updated
Mar 3, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.