Parent Partnership Project

NCT ID: NCT01789944

Last Updated: 2015-05-20

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 34 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-01-31
• Study Completion Date: 2014-08-31

Brief Summary

To evaluate the acceptability and feasibility of peers as interventionists in delivering family-based behavioral pediatric weight control intervention.

Detailed Description

A new model of delivering family-based pediatric overweight treatment that decreases costs but sustains short- and long-term efficacy is needed. One possible opportunity for this is a peer intervention model in which families receiving professionally-led intervention then subsequently providing intervention to other families. In addition, peer interventionists' continued engagement in the behavior change process through providing intervention to others could improve their own long-term efficacy. The project begins with the standard approach of having professional interventionists provide family-based behavioral pediatric overweight treatment to overweight children and their parent (1st generation families; n=30). Subsequently, half of 1st generation families will be randomly assigned to serve as peer interventionists to other overweight parents and children (2nd generation families; n=30). The remaining 1st generation families will neither receive nor provide any additional treatment. This project aims to develop the peer intervention training and delivery and then to examine the feasibility and acceptability of the peer intervention. This project also aims to derive an estimate of the efficacy of peer intervention (receiving and providing) both at the end of receiving treatment and 6 months later, as well as the impact of providing intervention on peer interventionists' weight outcomes.

Conditions

Childhood Obesity

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Provide Treatment

Peers provide treatment to 2nd generation following receipt of the intervention.

Group Type: EXPERIMENTAL

Behavioral: Family-based behavioral intervention

Intervention Type: BEHAVIORAL

This behavioral treatment includes behavioral skills training and accountability, including food and activity self-monitoring, goal setting, and home environment change

Treatment Only

Peers receive treatment and return for a 6-month follow-up

Group Type: EXPERIMENTAL

Behavioral: Family-based behavioral intervention

Intervention Type: BEHAVIORAL

This behavioral treatment includes behavioral skills training and accountability, including food and activity self-monitoring, goal setting, and home environment change

Interventions

Behavioral: Family-based behavioral intervention

This behavioral treatment includes behavioral skills training and accountability, including food and activity self-monitoring, goal setting, and home environment change

Intervention Type: BEHAVIORAL

Eligibility Criteria

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.

• Minimum Eligible Age: 7 Years
• Maximum Eligible Age: 11 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Seattle Children's Hospital

OTHER

Sponsor Role: lead

Responsible Party

Brian Saelens

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Seattle Children's

Seattle, Washington, United States

Countries

United States

Other Identifiers

1R21DK095676-01

Identifier Type: NIH

Identifier Source: org_study_id

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