Family Program for Weight Gain Prevention

Not Applicable

Completed

• Conditions: Overweight; Obesity
• Interventions: Behavioral: Control Group; Behavioral: Family Program for the Prevention of Weight Gain

• Registration Number: NCT00989170
• Lead Sponsor: University of Colorado, Denver

Brief Summary

The long-term goal of this project is to develop, evaluate, and disseminate to Extension Service families across the state of Colorado, an engaging, interactive, and evidence-based Family Program in order to prevent weight gain in adults and excess weight gain in children. Excess weight gain in children is defined as an increase in body weight beyond the increase in weight associated with normal growth and development. The program will focus on small, easily adopted, sustainable, lifestyle changes.

Project Objectives include:

1. Enhancing a Family Program by including food and physical activity environmental assessments, an online social network, and a pre-programmed health-based text messaging system, and by gaining feedback from extension families through a series of 6 focus groups.

2. Conducting a randomized trial to evaluate the impact of the enhanced Family Program on the prevention of weight gain in families with overweight children. The investigators hypothesize that excess weight gain will be prevented in subjects in the intervention group, while those in the control group will gain excess weight.

3. Disseminating the Family Program through USDA Cooperative Extension Services in Colorado and evaluate the usefulness/effectiveness of the program for USDA Extension agents and participating families. The investigators will conduct 4 additional focus groups at the end of this objective to gain feedback on its usefulness in a "real-life" setting. This objective is different from objective 2 in that the investigators are evaluating the program in a real-life setting, using qualitative and self-reported data, rather than conducting a clinical trial.

By conducting focus groups with Extension families during both objectives #1 and 3, the Family Program will help to improve knowledge regarding behavioral and environmental factors influencing obesity. After enhancing the Family Program (Objective #1), the investigators will test its effectiveness in a randomized study of 200 families (Objective #2). Finally, after having developed and tested this effective intervention strategy, the investigators will disseminate it through Extension Agents throughout the state to evaluate its usefulness in a "real-life" setting (Objective #3).

Detailed Description

Not available

Study Timeline

• Study Start: 2009-07
• Study First Submitted: 2009-10-01
• Study First Submitted QC: 2009-10-01
• Study First Posted: 2009-10-02
• Primary Completion: 2012-12
• Study Completion: 2012-12
• Status Verified: 2016-02
• Last Update Submitted: 2016-02-09
• Last Update Posted: 2016-02-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 418

Inclusion Criteria

• Families with at least one overweight child (8-12 years of age, BMI for age between the 84.6th and 95.4th percentile)

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Exclusion Criteria

• Individuals with physical or medical limitations that prevent them from engaging in physical activity. We will screen potential subjects and exclude subjects with an underlying disease that would inhibit activity using the Physical Activity Readiness Questionnaire (PAR-Q)
• Individuals using medication that influences body weight and appetite such as ADHD medication (e.g. Ritalin) and medication for depression.
• Pregnant and lactating women because their patterns of physical activity and eating may be different from their usual baseline. In the event a woman becomes pregnant during the study her data will not be included in the final analyses.
• Adults or children who are weight unstable due to weight loss surgery, weight loss medication, or dietary behavior.
• Families who do not have access to the internet at home or are not willing or able to use public access computers e.g., libraries and schools.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
No enhanced Family Program	Control Group	-
Family Program for the Prevention of Weight Gain	Family Program for the Prevention of Weight Gain	Use of an enhanced Family Program on the prevention of weight gain in families with overweight children.

Primary Outcome Measures

Name	Time	Method
The primary outcome of the randomized study is the proportion of overweight children who gain BMIp during the 6-month study period.	6 months

Trial Locations

Locations (1)

Center for Human Nutrition; 🇺🇸 Denver, Colorado, United States