NOURISH+: Nourishing Our Understanding of Role Modeling to Improve Support and Health

Not Applicable

Completed

• Conditions: Overweight and Obesity

• Registration Number: NCT01361243
• Lead Sponsor: Virginia Commonwealth University

Brief Summary

The purpose of this study is to evaluate the efficacy of a parent intervention (NOURISH+) aimed at reducing the problem of overweight and obesity in children.

Detailed Description

Pediatric overweight is a national public health concern. The percentage of overweight children in the U.S. between the ages of 5 and 11 has nearly tripled in the last 3 decades. African American children are particularly at risk. Pediatric overweight is associated with numerous physical and psychological health problems. Moreover, overweight children are at significant risk for obesity in adulthood. Thus, a focus on pediatric overweight is an important step in the prevention of adult obesity.

Despite the urgent need for pediatric overweight interventions, outcomes of some of the most rigorous treatments are, at best, mixed. Although research has found that including parents in interventions for pediatric overweight has positive effects on outcomes, parental involvement is usually limited. Moreover, relatively few studies have included sufficient numbers of lower-SES, African American participants, a group at increased risk for pediatric overweight and associated complications. This study will evaluate the efficacy of an intensive intervention targeting ethnically diverse parents of overweight, children ages 5-11 (NOURISH-Nourishing Our Understanding of Role Modeling to Improve Support and Health).

Study Timeline

• Study Start: 2011-04
• Study First Submitted: 2011-05-24
• Study First Submitted QC: 2011-05-24
• Study First Posted: 2011-05-26
• Primary Completion: 2018-01-31
• Study Completion: 2018-01-31
• Status Verified: 2018-02
• Last Update Submitted: 2018-02-21
• Last Update Posted: 2018-02-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 730

Inclusion Criteria

• Parents/caregivers must be at least 18 years old
• Parents/caregivers must have a child between the ages of 5 and 11 with a BMI > the 85th percentile, who primarily resides in the caregiver's home
• Parents/caregivers need to speak English, be able to follow basic instructions, and perform simple exercises

Exclusion Criteria

• Non-ambulatory parents/caregivers
• Pregnant parents/caregivers
• Parents/caregivers who have a medical condition that might be negatively impacted by exercise
• Parents/caregivers who have a psychiatric diagnosis that would impair their ability to respond to assessments or participate in a group
• Parents whose children have a medical or developmental condition that precludes weight loss using conventional diet and exercise methods

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Child BMI	baseline, post-testing, 4-month, and 10-month follow-up

Secondary Outcome Measures

Name	Time	Method
Parental BMI, dietary intake, and physical activity levels	baseline, post-testing, 4-month, and 10-month follow-up
Child dietary intake, quality of life, and physical activity	baseline, post-testing, 4-month, and 10-month follow-up

Trial Locations

Locations (1)

Virginia Commonwealth University; 🇺🇸 Richmond, Virginia, United States