Brief Motivational Interviewing to Reduce Child Body Mass Index

NCT01335308 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 645

Last updated 2023-10-13

Study results available
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Summary

BMi 2 is a study that tests a behavioral counseling approach to reduce obesity in children. Practitioners (Pediatricians, Nurse Practitioners) were randomly assigned to one of three groups. The first group continued with standard care; in group 2, each practitioner delivered four study Motivational Interviewing visits with the parent/caregiver, and in group 3 in addition to the practitioner, a registered dietitian delivered 6 Motivational Interviewing visits. The primary outcome will be the child's percentile BMI change between the baseline and 2-year follow-up. Secondary outcomes will include behavior change around fruits and vegetables, sweetened beverages and exercise. Our hypothesis is that there will be a larger decrease in BMI percentile for children in group 3 than in group 2, and that children in group 2 will have a decrease in BMI percentile when compared to group one.

Conditions

  • Childhood Obesity

Interventions

BEHAVIORAL

Standard Care

Practitioners will receive 2 hour obesity lecture and ½ day protocol training. Families recruited are given parent education materials. Outcomes will be collected at 1 year and 2 years after enrollment

BEHAVIORAL

Moderate Dose Motivational Interviewing

Practitioners receive 2 days of Motivational Interviewing and Behavioral Therapy Training and ½ day protocol training. Families recruited receive 4 x MI visits with the pediatric practitioner. Outcomes will be collected at 1 year and 2 years after enrollment

BEHAVIORAL

Higher Dose Motivational Interviewing

Practitioners receive 2 days of Motivational Interviewing and Behavioral Therapy Training and ½ day protocol training. Families recruited receive 4 x MI visits with the pediatric practitioner and 6 x visits (in phone or in person) with a Registered Dietitian, also trained in Motivational Interviewing. Outcomes will be collected at 1 year and 2 years after enrollment

Sponsors & Collaborators

Principal Investigators

  • Ken Resnicow, PhD · University of Michigan

  • Richard Wasserman, MD, MPH · University of Vermont, American Academy of Pediatrics

  • Erica Slora, PhD · American Academy of Pediatrics

  • Linda G Snetselaar, PhD · University of Iowa

  • Esther Myers, PhD · Academy of Nutrition and Dietetics

  • Fiona McMaster, MA, MPH · University of Michigan

  • Alison Bocian, MSc · American Academy of Pediatrics

  • Donna Harris, MA · American Academy of Pediatrics

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
2 Years
Max Age
10 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-10-31
Primary Completion
2013-07-31
Completion
2013-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01335308 on ClinicalTrials.gov