NCT06632171

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
81

participants targeted

Target at P50-P75 for not_applicable obesity

Timeline
Completed

Started Nov 2024

Shorter than P25 for not_applicable obesity

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
2 days until next milestone

First Posted

Study publicly available on registry

October 8, 2024

Completed
2 months until next milestone

Study Start

First participant enrolled

November 25, 2024

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 5, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 5, 2025

Completed
Last Updated

March 3, 2026

Status Verified

February 1, 2026

Enrollment Period

6 months

First QC Date

October 6, 2024

Last Update Submit

February 27, 2026

Conditions

Keywords

Emotional EatingResilienceObesityCognitive Behavioral TherapyMotivational Interviewing

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

EXPERIMENTAL

Obese individuals in this group receive the structured cognitive behavioral therapy-based and motivational interviewing-supported psychoeducation program.

Behavioral: Cognitive Behavioral Therapy- Based and Motivational Interviewing-Supported Psychoeducation

Control Group

NO INTERVENTION

Obese 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.

Psychoeducation Group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Muş State Hospital and Muş Central Healthy Life Center

Muş, Muş, 49000, Turkey (Türkiye)

Location

MeSH Terms

Conditions

ObesityEmotional Eating

Condition Hierarchy (Ancestors)

OverweightOvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and SymptomsFeeding BehaviorBehavior

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

Locations