Success in Health: Impacting Families Together (SHIFT)
Parents as Peer Interventionists in Treatment for Pediatric Weight Management
Study Overview
Status
Conditions
Detailed Description
The high prevalence of pediatric overweight and obesity in the U.S. necessitates the development of efficacious, but cost-effective and easily disseminable interventions that improve and sustain better pediatric weight outcomes. Accumulated evidence finds initial and long-term efficacy of moderate-to-high intensity (>25 contact hours) family-based treatment (FBT) for elementary school-aged children, but such treatment is prohibitively expensive because of high personnel costs (delivery by behavioral health professionals) and therefore limited in availability, reach, and impact. Very few overweight/obese children receive evidence-based treatment to improve their weight status or health.
The pilot data suggest a new model, peer-based delivery FBT with FBT-treated parents trained and subsequently delivering FBT to other families, is feasible and demonstrates initial efficacy. This delivery model could dramatically reduce FBT costs and increase FBT availability. Preliminary data also suggest that serving as a peer interventionist may also benefit the peers themselves and their children in better sustaining their own weight outcomes. The present study aims to provide a more definitive test of the short- and long-term efficacy of peer- versus professionally-delivered FBT on child weight outcomes. Embedded in this comparison is an examination of the feasibility of peer-based FBT delivery, investigating the impact of serving as a peer interventionist on the peers' own and their child's long- term weight status, and a more comprehensive examination of differential costs of professional- versus peer- based FBT delivery.
The present study will also test potential dissemination and sustainability by examining the efficacy of peer-delivered FBT among peer interventionists who themselves received FBT from other peers and not from professional interventionists. Moderation of treatment outcome is also examined, focusing on peer interventionist and child characteristics. This multi-phase trial will enroll 304 families with 7-11 year old overweight/obese children in multiple sites throughout the region, and include short-term (post-treatment) and long-term (up through 1 year after treatment cessation) assessments. This investigation of an innovative approach that could significantly reduce FBT delivery costs, while also improving the maintenance of treatment effects, is critical to improving the health of the many already overweight children at risk for chronic disease.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Washington
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Seattle, Washington, United States, 98121
- Seattle Children's
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Child age: 7-11 years at time of enrollment
- Overweight child: at or above 85th percentile for age- and gender-specific BMI.
- At least one overweight parent (BMI≥ 25.0).
- Parent is willing and able to actively participate in treatment including willingness to serve as a peer interventionist following treatment.
- Must live within 50 miles of the treatment center.
Exclusion Criteria:
- Current enrollment in another weight control program for the participating child or parent.
- The participating parent is pregnant.
- Thought disorder, suicidality, or substance abuse disorder in either the participating parent or the participating child.
- Inability of the child to comprehend English at a 1st-grade level or participating parent to comprehend English at an 8th-grade level.
- Physical disability or illness in either the participating parent or the child that precludes moderate intensity physical activity.
- Medication regimen for the child that affects his or her weight.
- Conditions known to promote obesity in the participating child (e.g. Prader-Willi).
- Diagnosed eating disorder (i.e., anorexia nervosa, bulimia nervosa, binge eating disorder) in either parent (participating and nonparticipating) and/or the participating child.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Pro.Treatment, Not a Peer
Families receive FBT for Pediatric Weight Management by Professionals interventionists and parents are NOT Peer Interventionists
|
This behavioral treatment includes behavioral skills training and accountability, including food and activity self-monitoring, goal setting, and home environment change.
This 20 week treatment is adapted from our existing evidence-based interventions and is delivered by PROFESSIONAL interventionists.
|
|
Experimental: Pro.Treatment, Peer
Families receive FBT for Pediatric Weight Management by Professionals and parents ARE Peer Interventionists
|
This behavioral treatment includes behavioral skills training and accountability, including food and activity self-monitoring, goal setting, and home environment change.
This 20 week treatment is adapted from our existing evidence-based interventions and is delivered by PROFESSIONAL interventionists.
Parents who receive FBT complete 6 weeks of training and then serve as peer interventionists to a new group of families.
|
|
Experimental: Peer Treatment, Not a Peer
Families receive FBT for Pediatric Weight Management by Peers and parents are NOT Peer Interventionists
|
This behavioral treatment includes behavioral skills training and accountability, including food and activity self-monitoring, goal setting, and home environment change.
This 20 week treatment is adapted from our existing evidence-based interventions and is provided by PEER interventionists.
|
|
Experimental: Peer Treatment, Peer
Families receive FBT for Pediatric Weight Management by Peers and parents ARE Peer Interventionists
|
Parents who receive FBT complete 6 weeks of training and then serve as peer interventionists to a new group of families.
This behavioral treatment includes behavioral skills training and accountability, including food and activity self-monitoring, goal setting, and home environment change.
This 20 week treatment is adapted from our existing evidence-based interventions and is provided by PEER interventionists.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Child BMI z-score
Time Frame: Baseline, 20 Weeks (post treatment), 6 and 12 months post treatment
|
BMI will be calculated as kg/m2 and children's BMI z-scores will be calculated using CDC growth charts.
|
Baseline, 20 Weeks (post treatment), 6 and 12 months post treatment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Costs of Peer Versus Professional Treatment
Time Frame: 20 weeks
|
Direct and indirect costs of associated with intervention using peer or professional interventionists.
Direct costs will be estimated using hours spent providing treatment of both peers and professionals who will track their time using an online application.
Costs associated with hours spent will be based on professional salaries or stipends provided to peer interventionists.
|
20 weeks
|
|
Change in Parent BMI
Time Frame: Baseline, 20 Weeks (post treatment), 6 and 12 months post treatment
|
BMI of parent will be calculated as kg/m2.
|
Baseline, 20 Weeks (post treatment), 6 and 12 months post treatment
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Brian E Saelens, PhD, Seattle Children's
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1R01DK104863-01A1 (U.S. NIH Grant/Contract)
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