Motivational Interviewing for Overweight and Obese Adults at Healthy Life Centers
MI-HLC
Effect of Motivational Interviewing on Anthropometric Measurements, eHealth Literacy, and Healthy Eating Attitudes Among Overweight and Obese Adults Attending Healthy Life Centers: A Randomized Controlled Trial
1 other identifier
interventional
54
1 country
3
Brief Summary
Overweight and obesity are major public health problems associated with increased morbidity and mortality. Motivational interviewing is a patient-centered counseling approach that may improve lifestyle behaviors and weight management. This randomized controlled trial aims to evaluate the effect of motivational interviewing on anthropometric measurements, eHealth literacy, and healthy eating attitudes among overweight and obese adults attending Healthy Life Centers in Sakarya, Türkiye. Participants will be randomly assigned to either a motivational interviewing intervention group or a routine nutrition counseling control group. Outcomes will be assessed at baseline and after the intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Sep 2026
3 active sites
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
July 30, 2026
CompletedFirst Posted
Study publicly available on registry
August 4, 2026
CompletedStudy Start
First participant enrolled
September 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2027
Study Completion
Last participant's last visit for all outcomes
April 1, 2028
August 4, 2026
July 1, 2026
4 months
July 30, 2026
July 30, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Body Weight
Body weight (kg) will be measured at baseline and after completion of the 12-week intervention using standardized anthropometric procedures. The primary outcome is the change in body weight from baseline to post-intervention.
Baseline and 12 weeks
Secondary Outcomes (5)
Change in Body Mass Index (BMI)
Baseline and 12 weeks
Change in Waist Circumference
Baseline and 12 weeks
Change in Waist-to-Hip Ratio
Baseline and 12 weeks
Change in eHealth Literacy
Baseline and 12 weeks
Change in Healthy Nutrition Attitudes
Baseline and 12 weeks
Study Arms (2)
Experimental Group
EXPERIMENTALParticipants will receive four structured motivational interviewing sessions in addition to routine nutrition counseling provided by Healthy Life Centers. The first and fourth sessions will be conducted face-to-face, and the second and third sessions will be delivered by telephone or online.
Control Group
ACTIVE COMPARATORParticipants will receive routine nutrition counseling according to standard Healthy Life Center practice without motivational interviewing.
Interventions
Participants will receive four structured motivational interviewing sessions in addition to routine nutrition counseling. The first and fourth sessions will be delivered face-to-face, while the second and third sessions will be conducted by telephone or online. The intervention is based on motivational interviewing principles and aims to improve healthy eating behaviors, eHealth literacy, and anthropometric outcomes among overweight and obese adults.
Participants will receive routine nutrition counseling provided by Healthy Life Centers according to standard clinical practice without motivational interviewing.
Eligibility Criteria
You may qualify if:
- Adults aged 18 years and older.
- Body mass index (BMI) ≥25 kg/m² (overweight or obese).
- Registered at one of the participating Healthy Life Centers in Sakarya Province.
- Able to communicate in Turkish.
- Willing to participate and provide written informed consent.
- Able to participate in face-to-face and telephone/online counseling sessions.
You may not qualify if:
- Pregnancy or breastfeeding.
- Severe psychiatric disorders or cognitive impairment affecting participation.
- Serious medical conditions preventing participation in lifestyle counseling.
- Currently participating in another behavioral or weight management intervention.
- Inability to complete follow-up assessments.
- Withdrawal of informed consent at any time.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sakarya Universitylead
- Sakarya Provincial Health Directoratecollaborator
Study Sites (3)
Adapazarı Healthy Life Center
Sakarya, Adapazarı, Turkey (Türkiye)
Sapanca Healthy Life Center
Sakarya, Sapanca, Turkey (Türkiye)
Serdivan Healthy Life Center
Sakarya, Serdivan, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- Outcome assessors will be blinded to group allocation to minimize assessment bias.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 30, 2026
First Posted
August 4, 2026
Study Start (Estimated)
September 1, 2026
Primary Completion (Estimated)
January 1, 2027
Study Completion (Estimated)
April 1, 2028
Last Updated
August 4, 2026
Record last verified: 2026-07