PACEAdol: PACE+: Counseling Adolescents for Exercise and Nutrition

Sponsor
University of California, San Diego (Other)
Overall Status
Completed
CT.gov ID
NCT01657422
Collaborator
San Diego State University (Other)
819
2
2
68
409.5
6

Study Details

Study Description

Brief Summary

PACE+ was developed to address the increased number of adolescents in our country that are at risk for cardiovascular disease, cancer, and other diseases due to inactivity, obesity, and malnourishment. PACE+ will evaluate the efficacy of an integrated clinical and home-based intervention to improve physical activity and nutrition behaviors in adolescents ages 11-15 over a period of 2 years.

This study is unique in that it will be one of the first to evaluate a combined physical activity and nutrition intervention for youth that revolves around the primary health care setting. The PACE+ intervention is particularly innovative in that three components - computer, provider counseling, and an extended home-based intervention - are unified through a common theoretical framework.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: PACE+
N/A

Detailed Description

Improved physical activity (PA) and nutrition behaviors in adolescents show great promise to reduce risk of cancers and other diseases. Fewer than 20% of adolescents meet recommendations for fat or fruits & vegetables consumption, and only 50% of adolescent girls and 67% of boys meet recommendations for vigorous PA. PACE+ will evaluate an integrated clinical and home-based intervention to improve physical activity (PA) and nutrition behaviors in adolescents. The intervention has three integrated components: a computer assessment and action planner; provider counseling; and 24 months of extended phone & mail contact. 768 male and female adolescents age 11 through 15; will be recruited from six healthcare settings. Subjects will be randomly assigned within practices to two successive one-year "doses" of PACE+ or a comparison condition involving counseling for sun protection behaviors. PACE+ assesses four behaviors: 1) dietary fat, 2) fruits & vegetable consumption, 3) physical activity, and 4) sedentary behavior. Primary behavioral outcomes, secondary outcomes, and selected mediators and process variables will be measured prior to the first office visit and at 6, 12 and 24 months. Primary outcomes will be measured by the 7-day physical activity recall and 3-day food record of fruits & vegetables and fat at 12 months. Secondary outcomes include adiposity, fitness, BMI, psychosocial mediators of change, and body image. Potential risks are psychological and physical, however the risks are slight and of low likelihood. Benefits include helping bring about healthier lifestyles to prevent weight gain and reduce premature morbidity and mortality due to cancer, cardiovascular disease and other health problems. This study will be the first to evaluate a combined physical activity and nutrition intervention for youth that revolves around the primary health care setting.

Study Design

Study Type:
Interventional
Actual Enrollment :
819 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
PACE+: Counseling Adolescents for Exercise and Nutrition
Study Start Date :
Aug 1, 2000
Actual Primary Completion Date :
Nov 1, 2004
Actual Study Completion Date :
Apr 1, 2006

Arms and Interventions

Arm Intervention/Treatment
Experimental: PACE+ Intervention

Intervention Group

Behavioral: PACE+
Patients assigned to the intervention group will receive intervention strategies over a the course of 2 years including: (1) completion of a 45-minute office-based computer program resulting in an assessment and action plan for improvement in physical activity and nutrition behaviors; (2) a provider counseling session immediately following the computerized assessment, followed by (3) 12 phone calls and 24 mailings over a 24-month period conducted by PACE+ staff members
Other Names:
  • PACE+ Intervention
  • No Intervention: Sun Protection

    Control / Comparison group. Patients assigned to the comparison group will receive intervention strategies over a the course of 2 years including: (1) completion of a 30-minute office-based computer program resulting in on-screen feedback to address excess sun exposure prevention, and (2) 4 phone calls and 4 mailings over a 24-month period conducted by PACE+ staff members.

    Outcome Measures

    Primary Outcome Measures

    1. Dietary fat, fruits & vegetable consumption [12months]

      Equal in importance to the other two primary outcome measures, physical activity and sedentary behaviors

    2. Physical activity [12 months]

      Equal in importance to the other two primary outcome measures, dietary fat, fruits and vegetables, and sedentary behaviors

    3. sedentary behavior [12 months]

      equal in importance to the other two primary outcome measures: physical activity and diet fat, fruits and vegetable consumption

    Secondary Outcome Measures

    1. dietary fat, fruits and vegetables [24 months]

      All were equal in terms of importance

    2. physical activity [24 months]

    3. sedentary behavior [24 months]

    Other Outcome Measures

    1. weight status [12 and 24 months]

      Both time points equally important

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    11 Years to 15 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Subjects must be in good general health and have the ability to read and speak English.
    Exclusion Criteria:
    • A known eating disorder,

    • pregnancy,

    • any cardiovascular or musculoskeletal problems that would limit their ability to comply with physical activity recommendations, and

    • being in foster care (due to difficulty in obtaining follow-up measures).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of California, San Diego La Jolla California United States 92093
    2 San Diego State University Foundation San Diego California United States 92128

    Sponsors and Collaborators

    • University of California, San Diego
    • San Diego State University

    Investigators

    • Principal Investigator: Kevin Patrick, MD, UCSD

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Kevin Patrick, MD, MS, Kevin Patrick, MD, MS, Principal Investigaor and Professor, University of California, San Diego
    ClinicalTrials.gov Identifier:
    NCT01657422
    Other Study ID Numbers:
    • 7R01CA081495-04
    First Posted:
    Aug 6, 2012
    Last Update Posted:
    Aug 6, 2012
    Last Verified:
    Aug 1, 2012
    Keywords provided by Kevin Patrick, MD, MS, Kevin Patrick, MD, MS, Principal Investigaor and Professor, University of California, San Diego

    Study Results

    No Results Posted as of Aug 6, 2012