Obesity Clinical Trial
Official title:
PACE-PC: Primary Care Management of Adolescent Obesity
This 12-month randomized controlled trial, sponsored by NIH/NCI, aims to reduce BMI in obese
adolescents (ages 11 -13) by intervening on physical activity and nutrition behaviors within
primary care settings.
PACE-PC is a theory-based stepped care program that enables pediatricians and primary care
providers to intervene with obese adolescents to improve their anthropometric, metabolic,
physiological, behavioral, and quality of life outcomes over a one-year period. The program
integrates clinician counseling, health educator counseling, and phone and mail contact. It
supports tailoring to the needs of obese adolescents and family members and promotes
improved diet and physical activity behaviors, weight loss, and ultimately weight loss
maintenance.
Participants will be randomly assigned to the Enhanced Usual Care or the PACE-PC stepped
care condition. The Enhanced Standard Care condition includes an initial visit and
counseling by a physician, 3 visits with a health educator, and materials on how to improve
weight related behaviors.
The PACE-PC Stepped Care condition includes 3 steps (each lasting 4 months), with the first
step being the most intensive:
Step 1 includes: a physician visit, monthly health educator visits, biweekly phone
counseling, and weekly dissemination of nutrition and physical activity information
Step 2 includes: a health educator visits every other month, biweekly phone counseling, and
weekly dissemination of nutrition and physical activity information
Step 3 includes: monthly phone counseling and weekly dissemination of nutrition and physical
activity information
Participants randomized to the PACE-PC condition will be enrolled in Step 1 (the most
intensive) for the first 4 months. Depending upon response at the end of Step 1, for the
next 4 months adolescents will be triaged to Step 2 (less intensive) or will repeat Step 1.
At 8 months, again based upon treatment response, triage will occur to either Step 3 (least
intensive) or repetition of the previous step.
| Status | Completed |
| Enrollment | 106 |
| Est. completion date | February 2011 |
| Est. primary completion date | February 2011 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 11 Years to 13 Years |
| Eligibility |
Inclusion Criteria: - Males and Females, ages 11-13 who are obese (> 95% Body Mass Index for age and gender). Participants must have: - a home telephone and permanent residence with the intent to stay in the San Diego area over the entire study period; - willingness to return to the pediatrician for counseling sessions; - ability to attend measurement visits at the PACE research office. Exclusion Criteria: - Any prospective participant with any comorbidities of obesity that require immediate sub-specialist referral including pseudotumor cerebri, sleep apnea, obesity hypoventilation syndrome, and orthopedic problems will be excluded from the study. - Additionally, participants will also be excluded if they are over 285 pounds (limits of DXA machine), have any pulmonary, cardiovascular or musculoskeletal problem that would limit ability to comply with moderate-level physical activity (e.g. walking), have a history of substance abuse, or other psychiatric disorder that would impair compliance with the study protocol, or are using any medications which alter body weight. - Patients in foster care will be ineligible due to difficulty in obtaining follow-up measures should they move from home to home. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
| Country | Name | City | State |
|---|---|---|---|
| United States | UCSD - CALIT2- Atkinson Hall | La Jolla | California |
| Lead Sponsor | Collaborator |
|---|---|
| University of California, San Diego |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Primary: The primary outcome of this study is to compare at 12 months, the effects of the PACE-PC intervention and enhanced standard care on BMI z-score among obese (> 95 percentile for age) male and female adolescents aged 11 -13. | baseline, 4 months, 8 months, 12 months | No | |
| Secondary | Secondary: Secondary outcomes will be: 1) anthropometric measures (BMI, waist circumference, body fat); 2) metabolic and physiological manifestations of obesity (fasting insulin, fasting blood glucose and blood lipid levels); 3) behavioral measurement | baseline, 4 mos, 8 mos, 12 mos | No |
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