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Dissemination and Implementation of the Bright Bodies Intervention for Childhood Obesity

Primary Purpose

Obesity, Childhood

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Bright Bodies
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity, Childhood focused on measuring Implementation science, Intensive lifestyle intervention, Pediatric obesity, Behavior modification, Body mass index

Eligibility Criteria

8 Years - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children ages 8-12 years with BMI ≥95th percentile and their parents;
  • Child-parent dyads enrolled in the Bright Bodies intervention at each site will be eligible for inclusion in the evaluation study.

Exclusion Criteria:

  • Children and/or parents who do not speak the language in which the program will be delivered at each site;
  • Children and/or parents who plan to move away from the area within the next 15 months;
  • Children with a history of purging and/or dramatic weight loss prior to the trial;
  • Children who are currently participating in another high-intensity lifestyle intervention or other similar research study, or are planning to have bariatric surgery within the next six months
  • Children whose EHR data cannot be accessed by the study teams;
  • Children with chronic medical conditions limiting their ability to take food by mouth (e.g., g-tube fed, total parenteral nutrition), participate in physical activity (e.g., wheelchair bound), or meaningfully participate in group sessions (e.g., cognitive impairment);
  • Children with a sibling enrolled in the trial

Sites / Locations

  • University of Alabama at BirminghamRecruiting
  • University of California San FranciscoRecruiting
  • Maine Medical CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intervention

Arm Description

Bright Bodies

Outcomes

Primary Outcome Measures

Change in %BMIp95
Change in %BMIp95, calculated from height and weight. A negative percentage indicates that the participant's BMI has decreased since enrollment.

Secondary Outcome Measures

Change in parent BMI
Change in BMI, calculated from height and weight measured as part of the Bright Bodies program. A negative change in parent BMI indicates that the parent's BMI has decreased since enrollment.
Change in weight-related quality of life
Sizing Them Up is a validated, parent-proxy reported instrument assessing weight-related quality of life for children aged 5-13 years. Possible score ranges from 1 (never) to 4 (always). Higher score indicates a higher quality of life.
Change in weight-related health behaviors.
Parent-proxy responses to the Bright Bodies Healthy Lifestyles Questionnaire about vegetable and fruit intake [scores range from 1 (none) to 4 (three or more); Higher score indicates healthier behavior]; sugar-sweetened beverage intake [scores range from 1 (none) to 4 (three or more); Lower score indicates healthy behavior]; intake of sweets/desserts [scores range from 1 (none) to 4 (seven or more); Lower score indicates healthy behavior]; physical activity [scores range from 1 (less than 30 minutes) to 4 (more than 2 hours); higher score indicates healthy behavior.]; screen time [scores range from 1 (more than 4 hours) to 4 (1 hour or less); higher score indicates healthy behavior.]; sleep [scores range from 1 (6 hours or less) to 3 (9 hours or more) for the amount a child sleeps each night and from 1 (no) to 2 (yes) for the question about a regular bedtime; Higher score indicates healthy behavior].
Change in binge eating behaviors.
Children's Brief Binge-Eating Questionnaire will be parent-proxy reported. Possible score ranges from 1 (definitely false) to 3 (definitely true). Higher scores indicate greater concern for binge eating behavior.
Change in parent conversations about weight.
Parent conversation about weight is measured with three questions using a parent self-report instrument from the New Moves, a school-based intervention designed to prevent obesity and other weight-related problems. Possible scores range from 1 (never) to 5 (very often). Lower score indicates less weight talk.
Per patient cost for participation in Bright Bodies
Calculated based on data regarding resource utilization of the Bright Bodies program and participants' use of relevant medical and non-medical resources.

Full Information

First Posted
October 20, 2022
Last Updated
April 28, 2023
Sponsor
Yale University
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT05595161
Brief Title
Dissemination and Implementation of the Bright Bodies Intervention for Childhood Obesity
Official Title
Dissemination and Implementation of the Bright Bodies Intervention for Childhood Obesity
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 11, 2022 (Actual)
Primary Completion Date
August 1, 2025 (Anticipated)
Study Completion Date
August 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yale University
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will evaluate the effectiveness of the Bright Bodies intervention in improving body mass index (BMI) among 8-12 year-old children with obesity simultaneously with the impact of the implementation strategy on adoption, reach, fidelity, cost, and maintenance of the intervention in three heterogenous settings serving patients disproportionately affected by obesity.
Detailed Description
The demonstrated efficacy of Bright Bodies in a well-designed randomized controlled trial (RCT) and a real-world effectiveness study reduce equipoise and challenge the ethics of a prospective RCT of implementing Bright Bodies in other settings. As such, this study is an observational, multiphase mixed methods design to evaluate effectiveness and implementation among three purposively selected heterogeneous sites serving low-income populations with racial and ethnic, rural-urban, and geographic diversity. Children ages 8-12 years with BMI ≥95th percentile and their parent/caregivers hereafter referred to as parent will be recruited to participate in the evaluation study from among participants in the newly-established Bright Bodies programs at each of the three implementation sites. The aim is for each site to recruit approximately 40 children and their parents (a total of 120 children and 120 parents) to participate in the Bright Bodies program over the study's enrollment period. The primary outcome is change in BMI expressed as a percentage of the 95th percentile (%BMIp95) using EHR data collected as part of routine clinical care up to 36 months before and up to 15 months after enrollment in the intervention. Secondary outcomes include: (a) change in %BMIp95 at three and six months, (b) changes in parent BMI at three and six months, (d) parent-reported changes in health behaviors (sleep, physical activity, screen time, eating behaviors), via surveys at 3, 6 and 12 months, and (e) changes in parent-proxy reported weight-related quality of life, parent stress, and parent talk about weight via surveys at baseline, 6, and 12 months after enrollment. We will also describe implementation outcomes (reach, adoption, fidelity/adaptation, and cost) through qualitative and quantitative data collection from members of our study team throughout the process of implementation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Childhood
Keywords
Implementation science, Intensive lifestyle intervention, Pediatric obesity, Behavior modification, Body mass index

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
240 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Bright Bodies
Intervention Type
Behavioral
Intervention Name(s)
Bright Bodies
Other Intervention Name(s)
SmartMoves TM (name of the curriculum used in the Bright Bodies intervention)
Intervention Description
The Bright Bodies intensive, family-based lifestyle intervention uses group sessions including nutrition education, behavior modification, and exercise to improve weight and weight-related outcomes among children and adolescents with obesity.
Primary Outcome Measure Information:
Title
Change in %BMIp95
Description
Change in %BMIp95, calculated from height and weight. A negative percentage indicates that the participant's BMI has decreased since enrollment.
Time Frame
Up to 36 months prior to baseline through up to 15 months after enrollment
Secondary Outcome Measure Information:
Title
Change in parent BMI
Description
Change in BMI, calculated from height and weight measured as part of the Bright Bodies program. A negative change in parent BMI indicates that the parent's BMI has decreased since enrollment.
Time Frame
Baseline through 6 months after enrollment
Title
Change in weight-related quality of life
Description
Sizing Them Up is a validated, parent-proxy reported instrument assessing weight-related quality of life for children aged 5-13 years. Possible score ranges from 1 (never) to 4 (always). Higher score indicates a higher quality of life.
Time Frame
Baseline through 12 months after enrollment
Title
Change in weight-related health behaviors.
Description
Parent-proxy responses to the Bright Bodies Healthy Lifestyles Questionnaire about vegetable and fruit intake [scores range from 1 (none) to 4 (three or more); Higher score indicates healthier behavior]; sugar-sweetened beverage intake [scores range from 1 (none) to 4 (three or more); Lower score indicates healthy behavior]; intake of sweets/desserts [scores range from 1 (none) to 4 (seven or more); Lower score indicates healthy behavior]; physical activity [scores range from 1 (less than 30 minutes) to 4 (more than 2 hours); higher score indicates healthy behavior.]; screen time [scores range from 1 (more than 4 hours) to 4 (1 hour or less); higher score indicates healthy behavior.]; sleep [scores range from 1 (6 hours or less) to 3 (9 hours or more) for the amount a child sleeps each night and from 1 (no) to 2 (yes) for the question about a regular bedtime; Higher score indicates healthy behavior].
Time Frame
Baseline through 12 months after enrollment
Title
Change in binge eating behaviors.
Description
Children's Brief Binge-Eating Questionnaire will be parent-proxy reported. Possible score ranges from 1 (definitely false) to 3 (definitely true). Higher scores indicate greater concern for binge eating behavior.
Time Frame
Baseline through 12 months after enrollment
Title
Change in parent conversations about weight.
Description
Parent conversation about weight is measured with three questions using a parent self-report instrument from the New Moves, a school-based intervention designed to prevent obesity and other weight-related problems. Possible scores range from 1 (never) to 5 (very often). Lower score indicates less weight talk.
Time Frame
Baseline through 12 months after enrollment
Title
Per patient cost for participation in Bright Bodies
Description
Calculated based on data regarding resource utilization of the Bright Bodies program and participants' use of relevant medical and non-medical resources.
Time Frame
From enrollment through 12 months after enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children ages 8-12 years with BMI ≥95th percentile and their parents; Child-parent dyads enrolled in the Bright Bodies intervention at each site will be eligible for inclusion in the evaluation study. Exclusion Criteria: Children and/or parents who do not speak the language in which the program will be delivered at each site; Children and/or parents who plan to move away from the area within the next 15 months; Children with a history of purging and/or dramatic weight loss prior to the trial; Children who are currently participating in another high-intensity lifestyle intervention or other similar research study, or are planning to have bariatric surgery within the next six months Children whose EHR data cannot be accessed by the study teams; Children with chronic medical conditions limiting their ability to take food by mouth (e.g., g-tube fed, total parenteral nutrition), participate in physical activity (e.g., wheelchair bound), or meaningfully participate in group sessions (e.g., cognitive impairment); Children with a sibling enrolled in the trial
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mahnoosh (Mona) Sharifi, MD, MPH
Phone
(203) 785-7821
Email
mona.sharifi@yale.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Emily B Finn, MPH
Email
e.finn@yale.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mahnoosh (Mona) Sharifi, MD, MPH
Organizational Affiliation
Yale University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alabama at Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233-1711
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Heather A Austin, PhD
Email
heatheraustin@uabmc.edu
Facility Name
University of California San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Amy L Beck, MD, MPH
Phone
415-476-3368
Email
amy.beck@ucsf.edu
Facility Name
Maine Medical Center
City
Portland
State/Province
Maine
ZIP/Postal Code
04101
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Abby Fleisch, MD, MPH
Phone
207-661-7602
Email
Abby.Fleisch@mainehealth.org

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Dissemination and Implementation of the Bright Bodies Intervention for Childhood Obesity

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