Challenge!, a Health Promotion/ Obesity Prevention Program for Teens

Sponsor
University of Maryland, Baltimore (Other)
Overall Status
Completed
CT.gov ID
NCT00746083
Collaborator
Annie E. Casey Foundation (Other), The Thomas Wilson Sanitarium for Children of Baltimore City (Other), Johns Hopkins Bloomberg School of Public Health (Other), University of Massachusetts, Worcester (Other)
235
1
2
69
3.4

Study Details

Study Description

Brief Summary

The purpose of Challenge! is to determine if adolescents enrolled in a health promotion/ obesity prevention program will have a healthier BMI-for-age z-score and body composition (body fat %), will consume a healthier diet, and engage in higher levels of physical activity compared to those that did not receive the intervention over time.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Challenge!
N/A

Detailed Description

Pediatric overweight is a major public health problem in the US, with the prevalence of overweight among children of all ages increasing dramatically over the past several decades. Interventions aimed at reducing the increased weight gain during adolescence have produced mixed results.

Challenge! is a randomized controlled trial for health promotion/ obesity prevention targeting low-income, urban, African American adolescents. Healthy adolescents were recruited from an urban medical center and from local middle schools. Weight status was not part of the inclusion criteria.

The intervention was home- and community-based and delivered one-on-one to each adolescent by a college-age "personal trainer". The intervention focused on goal-setting, consuming a healthy diet (increase fruits, vegetables, and water, and decrease high-fat snack and convenience foods), and increasing physical activity. We hypothesized that the teens enrolled in the intervention would have a healthier BMI-for-age z-score and a healthier body composition (body fat %) compared to those that did not receive the intervention over time. Additionally, we hypothesized that those enrolled in the intervention would consume healthier diets and have higher levels of physical activity compared to those that did not receive the intervention over time.

Study Design

Study Type:
Interventional
Actual Enrollment :
235 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Randomized Controlled Trial for Health Promotion/ Obesity Prevention Targeting Low-income, Urban, African-American Adolescents
Study Start Date :
Apr 1, 2001
Actual Primary Completion Date :
Jul 1, 2005
Actual Study Completion Date :
Jan 1, 2007

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention group

Behavioral: Challenge!
Each adolescent in the intervention group received 12 lessons administered in adolescent's home or community by a "personal trainer" (a college-aged mentor). The lessons focused on behavior change relating to diet and physical activity and was based on social cognitive theory. At the end of each lesson the adolescent set a behavior change goal for themselves. The adolescents were taught how to track their goals and they discussed thir ability/inability to meet their goals at each meeting with their personal trainer.
Other Names:
  • Obesity prevention
  • Goal setting
  • Diet
  • Physical activity
  • No Intervention: Control group

    Outcome Measures

    Primary Outcome Measures

    1. BMI-for-age z-score and percentiles (measured weight and height, self-reported gender and date of birth)and Body composition (Dual Energy X-ray Absorptiometry, and Bioelectrical Impedance Analysis) [2 years]

    Secondary Outcome Measures

    1. Physical Activity (accelerometry and self-report) Diet (Food frequency questionnaire) [2 years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    11 Years to 16 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Ages 11-16, willing to participate in a randomized controlled trial for health promotion
    Exclusion Criteria:
    • Outside of age range

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Maryland School of Medicine Baltimore Maryland United States 21201

    Sponsors and Collaborators

    • University of Maryland, Baltimore
    • Annie E. Casey Foundation
    • The Thomas Wilson Sanitarium for Children of Baltimore City
    • Johns Hopkins Bloomberg School of Public Health
    • University of Massachusetts, Worcester

    Investigators

    • Principal Investigator: Maureen M Black, PhD, University of Maryland School of Medicine, Department of Pediatrics, United States

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Maureen Black, Professor, University of Maryland, Baltimore
    ClinicalTrials.gov Identifier:
    NCT00746083
    Other Study ID Numbers:
    • H-21033
    • R40MC00241, M01 RR16500
    First Posted:
    Sep 3, 2008
    Last Update Posted:
    Aug 16, 2019
    Last Verified:
    Aug 1, 2019
    Keywords provided by Maureen Black, Professor, University of Maryland, Baltimore
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 16, 2019