NCT07745231

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

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
54

participants targeted

Target at P25-P50 for not_applicable

Timeline
19mo left

Started Sep 2026

Geographic Reach
1 country

3 active sites

Status
not yet recruiting

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

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 4, 2026

Completed
28 days until next milestone

Study Start

First participant enrolled

September 1, 2026

Expected
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2027

1.2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2028

Last Updated

August 4, 2026

Status Verified

July 1, 2026

Enrollment Period

4 months

First QC Date

July 30, 2026

Last Update Submit

July 30, 2026

Conditions

Keywords

Motivational InterviewingeHealth LiteracyHealthy EatingNutrition CounselingWeight ManagementRandomized Controlled TrialPrimary Health CareHealthy Life CenterBehavioral Intervention

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

EXPERIMENTAL

Participants 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.

Behavioral: Motivational InterviewingBehavioral: Routine Nutrition Counseling

Control Group

ACTIVE COMPARATOR

Participants will receive routine nutrition counseling according to standard Healthy Life Center practice without motivational interviewing.

Behavioral: Routine Nutrition Counseling

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.

Experimental Group

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

Control GroupExperimental Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (3)

Adapazarı Healthy Life Center

Sakarya, Adapazarı, Turkey (Türkiye)

Location

Sapanca Healthy Life Center

Sakarya, Sapanca, Turkey (Türkiye)

Location

Serdivan Healthy Life Center

Sakarya, Serdivan, Turkey (Türkiye)

Location

MeSH Terms

Conditions

OverweightObesity

Interventions

Motivational Interviewing

Condition Hierarchy (Ancestors)

OvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Directive CounselingCounselingMental Health ServicesBehavioral Disciplines and ActivitiesHealth ServicesHealth Care Facilities Workforce and Services

Central Study Contacts

Rıdvan ATICI, MSc

CONTACT

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
Model Details: Participants will be randomly assigned in a 1:1 ratio to either a motivational interviewing intervention group or a routine nutrition counseling control group. The intervention group will receive four structured motivational interviewing sessions in addition to routine care, while the control group will receive routine nutrition counseling only. Both groups will be followed in parallel throughout the study.
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

Locations