The Effect of Motivational Interviewing on Anthropometric Measurements, Eating Attitudes, and Cardiometabolic Index in Overweight and Obese Patients
1 other identifier
interventional
80
0 countries
N/A
Brief Summary
The Effect of Motivational Interviewing on Anthropometric Measurements, Eating Attitudes, and Cardiometabolic Index in Overweight and Obese Patients
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2025
Shorter than P25 for not_applicable
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
April 17, 2025
CompletedFirst Posted
Study publicly available on registry
April 27, 2025
CompletedStudy Start
First participant enrolled
May 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2025
CompletedApril 27, 2025
April 1, 2025
3 months
April 17, 2025
April 24, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
CMI
Cardiometabolic index
three months
Study Arms (2)
experimental group
ACTIVE COMPARATORIn addition to the procedures applied to the control group, the experimental group was also subjected to motivational interviewing
Control
ACTIVE COMPARATORThe 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.
Interventions
A calorie-restricted diet was implemented in both the intervention and control groups.
A moderate-intensity aerobic exercise program, consisting of 30-minute sessions five days per week, was implemented in both groups
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- Current use of medications known to induce weight gain or loss
- Presence of a diagnosed chronic illness
- Pregnancy or being in the lactation period."
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
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
- Principal Investigator
Study Record Dates
First Submitted
April 17, 2025
First Posted
April 27, 2025
Study Start
May 1, 2025
Primary Completion
August 1, 2025
Study Completion
August 1, 2025
Last Updated
April 27, 2025
Record last verified: 2025-04