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Motivational Interviewing for Overweight and Obese Adults at Healthy Life Centers

NCT07745231 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-09
Last updated
2026-08-04

Condition(s) studied

OverweightObesity

Investigational drug(s) / intervention(s)

Motivational InterviewingRoutine Nutrition Counseling

Motivational Interviewing: 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.

Routine Nutrition Counseling: Participants will receive routine nutrition counseling provided by Healthy Life Centers according to standard clinical practice without motivational interviewing.

Study 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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * 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. Exclusion Criteria: * 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.

Primary outcome measure(s)

  • Change in Body Weight — Baseline and 12 weeks
    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.

Trial sites (3)

FacilityCityRegionStatus
Adapazarı Healthy Life Center Sakarya Adapazarı
Sapanca Healthy Life Center Sakarya Sapanca
Serdivan Healthy Life Center Sakarya Serdivan
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07745231 on ClinicalTrials.gov ↗ ← All trials in Turkey