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NCT Number: NCT06947798

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

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

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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

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

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."

Treatment and study plan

Motivational Interviewing

Behavioral

motivational interviewing four times

Diet

Other

A calorie-restricted diet was implemented in both the intervention and control groups.

Physical exercise

Behavioral

A moderate-intensity aerobic exercise program, consisting of 30-minute sessions five days per week, was implemented in both groups

Primary outcomes

  1. CMI

    Time frame: three months

    Cardiometabolic index

Study contacts

Contact information is provided by the study sponsor or research team.

ORHUN DONMEZ

CONTACT

[email protected]

+905057397294

Sponsors and collaborators

Lead sponsor

Saltuklu Aile Sağlığı Merkezi

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Apr 27, 2025
Registry last updated
Apr 27, 2025

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.

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