Brief Motivational Interviewing to Reduce Child Body Mass Index

Not Applicable

Completed

• Conditions: Childhood Obesity
• Interventions: Behavioral: Moderate Dose Motivational Interviewing; Behavioral: Higher Dose Motivational Interviewing; Behavioral: Standard Care

• Registration Number: NCT01335308
• Lead Sponsor: University of Michigan

Brief 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.

Detailed Description

The study is a cluster-randomized intervention trial with clinical practices serving as the unit of randomization and analysis. The investigators are testing two increasingly intensive interventions compared to a minimal intensity/Usual Care Group. Group 1 (Usual Care) includes determination of BMI percentile at baseline, 1-year, and 2-year follow-up. Usual Care (UC) practitioners provide parents with educational materials and routine care. UC pediatricians and their study staff received a ½ day study orientation session which included a brief CME-type workshop addressing obesity treatment.. Group 2 (Pediatric Practitioner only) includes the same assessment points as UC. In addition, Group 2 Pediatric Practitioners (PPs) received 2 days of in-person training in Motivational Interviewing (MI) and Behavior Therapy (BT) as well as an interactive DVD MI booster training system focusing on pediatric obesity. PPs in Group 2 are asked to schedule 3 proactive counseling sessions with a parent of the index child in Year 1 and one additional "booster" visit in year 2. To guide their counseling they are provided with a food and activity screening tool. In addition, Group 2 practices are provided with educational materials written in a style consistent with Motivational Interviewing and Self Determination Theory. Unlike in Group 1, where all of the educational materials are provided proactively to each parent, in Groups 2 and 3, materials are distributed on a more selective tailored basis depending on parent needs. Group 3 (PP+RD) includes the same intervention components as Group 2, but adds MI-based counseling from a trained and registered dietitian (RD) who is linked to that practice. RDs deliver 6 MI-based counseling sessions over 2 years. The intervention is front loaded with 4 sessions in Year 1 and the remaining 2 in Year 2. The RD sessions are delivered both in-person (required for visit 1) and optionally by telephone or in-person, subsequently. Similar to MDs, RDs received 2.0 days of in-person MI and BT training, and the interactive DVD MI booster training system.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2009-10
• Study First Submitted: 2011-04-12
• Study First Submitted QC: 2011-04-13
• Study First Posted: 2011-04-14
• Primary Completion: 2013-07
• Study Completion: 2013-12
• Results First Submitted: 2016-10-28
• Results First Submitted QC: 2017-04-26
• Results First Posted: 2017-06-27
• Status Verified: 2023-10
• Last Update Submitted: 2023-10-11
• Last Update Posted: 2023-10-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 645

Inclusion Criteria

• 85th - 97th percentile BMI
• parent/care giver ability to converse in English
• working telephone

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Exclusion Criteria

• child under current subspecialty care for overweight/obesity
• child currently taking weight-altering medication (at enrollment)

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Moderate Dose Motivational Interviewing	Moderate Dose Motivational Interviewing	MI delivered by PCP, 4 sessions
Higher Dose Motivational Interviewing	Higher Dose Motivational Interviewing	MI delivered by PCP, 4 sessions plus MI delivered by RD, 6 sessions
Standard Care with Education Materials	Standard Care	Measure height and weight only. usual care

Primary Outcome Measures

Name	Time	Method
Child BMI Percentile	2 years after recruitment

Secondary Outcome Measures

Name	Time	Method
Change in Physical Activity	2 years after enrollment
Sweetened Beverage Consumption	2 years after enrollment
Fruit/Vegetable Consumption	2 years after enrollment

Trial Locations

Locations (1)

Pediatric Research in Office Settings; 🇺🇸 Elk Grove Village, Illinois, United States