Clinical Trials Directory

Trials / Completed

CompletedNCT03177148

Population Effects of MI on Pediatric Obesity in Primary Care

Population Effects of Motivational Interviewing on Pediatric Obesity in Primary Care

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
352 (actual)
Sponsor
University of Michigan · Academic / Other
Sex
All
Age
3 Years – 11 Years
Healthy volunteers
Accepted

Summary

In this cluster randomized effectiveness trial, pediatric primary care practices will be recruited from the American Academy of Pediatrics' national Pediatric Research in Office Settings (PROS) practice-based research network, as well as the client database of the Physician's Computer Company (PCC) - an Electronic Health Record (EHR) vendor. We will recruit 18 practices. 9 practices will be randomized to the Intervention arm and 9 practices to Usual Care. Intervention arm practices will select 1-2 pediatric clinicians, including pediatricians (PED) and nurse practitioners (NP), to receive in-person training in Motivational Interviewing (MI), behavioral therapy, billing and coding, and study procedures. Usual Care practices will select 1-2 pediatric clinicians to receive billing / coding and study protocol training only, via telephone and webinar; they will be offered in-person MI training at the close of the trial. Around 316 parents of overweight or obese children (BMI \> 85th percentile for age and gender) between 3 and 11 years of age at baseline that are patients of participating Intervention arm clinicians will be enrolled. Over 24 months, these parents may receive up to 4 in-person, MI-based counseling sessions with a trained pediatric clinician and up to 6 telephone counseling sessions with an MI-trained Registered Dietician (RD). There will be no study-specific contact with parents or their children in Usual Care practices during the trial - they will continue to receive usual care. EHR and billing data for all 3-11 year old children within all participating practices will be extracted by PCC to permit determination of the effectiveness of the intervention versus usual care on change in BMI z-score among 3 groups: 1) all eligible children in the Intervention arm), 2) all eligible children whose parent actively participates in the trial , and 3) all 3-11 year old children in all participating practices.

Conditions

Interventions

TypeNameDescription
BEHAVIORALIntervention by Clinicians•Parents will complete surveys after enrollment and at the end of intervention and participate in intervention visits by pediatric clinicians and telephonic counseling with Registered Dietitians (RDs). Intervention by pediatric clinicians: up to 4 sessions of MI, in-person Intervention by RDs: up to 6 sessions of MI via telephone.
BEHAVIORALUsual CarePediatric clinicians provide care as normal

Timeline

Start date
2017-07-01
Primary completion
2021-01-31
Completion
2021-08-31
First posted
2017-06-06
Last updated
2024-07-16
Results posted
2024-07-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03177148. Inclusion in this directory is not an endorsement.