- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01657422
PACE+: Counseling Adolescents for Exercise and Nutrition (PACEAdol)
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.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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California
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La Jolla, California, United States, 92093
- University of California, San Diego
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San Diego, California, United States, 92128
- San Diego State University Foundation
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: PACE+ Intervention
Intervention Group
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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:
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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.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dietary fat, fruits & vegetable consumption
Time Frame: 12months
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Equal in importance to the other two primary outcome measures, physical activity and sedentary behaviors
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12months
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Physical activity
Time Frame: 12 months
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Equal in importance to the other two primary outcome measures, dietary fat, fruits and vegetables, and sedentary behaviors
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12 months
|
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sedentary behavior
Time Frame: 12 months
|
equal in importance to the other two primary outcome measures: physical activity and diet fat, fruits and vegetable consumption
|
12 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
dietary fat, fruits and vegetables
Time Frame: 24 months
|
All were equal in terms of importance
|
24 months
|
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physical activity
Time Frame: 24 months
|
24 months
|
|
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sedentary behavior
Time Frame: 24 months
|
24 months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
weight status
Time Frame: 12 and 24 months
|
Both time points equally important
|
12 and 24 months
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Kevin Patrick, MD, UCSD
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 7R01CA081495-04 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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-
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