The Effect of Motivational Interviewing on Anthropometric Measurements, Eating Attitudes, and Cardiometabolic Index in Overweight and Obese Patients

April 24, 2025 updated by: ORHUN DÖNMEZ, Saltuklu Aile Sağlığı Merkezi
The Effect of Motivational Interviewing on Anthropometric Measurements, Eating Attitudes, and Cardiometabolic Index in Overweight and Obese Patients

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

Participants were randomly assigned into two groups-an Intervention Group (n = 40) and a Control Group (n = 40)-using block randomization through the website "random.org." Data were collected using a Personal Information Form, the Eating Behavior Disorder Scale, Anthropometric Measurements (body weight, body mass index, waist circumference, waist/hip ratio), and the Cardiometabolic Index. Both groups received routine recommendations, which included a daily caloric restriction of 500 kcal and moderate-intensity aerobic exercise for 30 minutes, five days a week.Motivational interviewing was administered to the intervention group through individual sessions, held once every two weeks, for a total of four sessions, each lasting 15 minutes. The interviews were conducted in the Education Room of the Saltuklu Family Health Center. After the motivational interviewing intervention was completed, post-tests (Eating Behavior Disorder Scale, Anthropometric Measurements, and Cardiometabolic Index) were administered to both groups. All participants were followed for a period of three months.

Study Type

Interventional

Enrollment (Estimated)

80

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Body Mass Index (BMI) in the range of 25 to 34.9 kg/m² was considered as an inclusion criterion

  • Being between 20 and 40 years of age (corresponding to the young adulthood period according to Erikson)

    -- Participants were required to be registered with the Saltuklu Family Health Center.

  • Willingness to participate in the study and provision of informed consent were required

Exclusion Criteria:

  • Current use of medications known to induce weight gain or loss
  • Presence of a diagnosed chronic illness
  • Pregnancy or being in the lactation period."

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: experimental group
In addition to the procedures applied to the control group, the experimental group was also subjected to motivational interviewing
Behavioral: motivational interviewing
motivational interviewing four times
Other: Diet
A calorie-restricted diet was implemented in both the intervention and control groups.
Behavioral: Physical exercise
A moderate-intensity aerobic exercise program, consisting of 30-minute sessions five days per week, was implemented in both groups
Active Comparator: Control
The control group received a dietary intervention involving a daily caloric restriction and was instructed to engage in moderate-intensity aerobic exercise for 30 minutes, five times per week.
Other: Diet
A calorie-restricted diet was implemented in both the intervention and control groups.
Behavioral: Physical exercise
A moderate-intensity aerobic exercise program, consisting of 30-minute sessions five days per week, was implemented in both groups

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
CMI
Time Frame: three months
Cardiometabolic index
three months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Saltuklu Aile Sağlığı Merkezi

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

May 1, 2025

Primary Completion (Estimated)

August 1, 2025

Study Completion (Estimated)

August 1, 2025

Study Registration Dates

First Submitted

April 17, 2025

First Submitted That Met QC Criteria

April 24, 2025

First Posted (Actual)

April 27, 2025

Study Record Updates

Last Update Posted (Actual)

April 27, 2025

Last Update Submitted That Met QC Criteria

April 24, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Saltuklu ASM

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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