Primary Care Research Network for the Treatment of Adolescent Obesity (TEENS)
Primary Purpose
Obesity
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Family-Based Lifestyle Modification
Family-Based Lifestyle Modification Program
Sponsored by
About this trial
This is an interventional treatment trial for Obesity focused on measuring Adolescents, Obesity, Weight Management, Family-based Lifestyle Modification
Eligibility Criteria
Inclusion Criteria:
- Male or female adolescents
- Age 12 to 16 years
- Body Mass Index (BMI) of 28 kg/m2
- Adolescent expresses desire to lose weight
- Parent willing to participate
- Live within 40 minutes from study clinic at CHOP or 60 minutes at Geisinger
Exclusion Criteria:
- Uncontrolled hypertension (blood pressure > 140/90 mm HG)
- Diabetes mellitus (fasting glucose > 126 mg/dl)
- Any serious uncontrolled medical disorder that would complicate participation in a weight loss program
- Bipolar disorder or psychosis (depression ok if adolescent is receiving treatment)
- Use of any medication affecting body weight, appetite or metabolism within 30 days prior to the start of treatment
- Positive pregnancy test at medical evaluation
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Group Condition
Self-Guided Condition
Arm Description
Outcomes
Primary Outcome Measures
Percentage change in initial body mass index (BMI) at 12 months
Secondary Outcome Measures
Compare mean reduction in percentage of initial BMI in the two treatments within each ethnic group/site (CHOP: urban African American adolescents and GHS: rural Caucasian adolescents
Compare the effectiveness of the two treatment approaches on improving risk factors for cardiovascular disease and diabetes (Total, HDL, and LDL cholesterol, triglycerides, glucose, insulin, and blood pressure) and on improving liver function
Compare mean reduction in percentage of initial BMI in each treatment group at month 6
Full Information
NCT ID
NCT01073215
First Posted
February 19, 2010
Last Updated
February 17, 2012
Sponsor
Children's Hospital of Philadelphia
Collaborators
Pennsylvania Department of Health, Geisinger Clinic, University of Pennsylvania
1. Study Identification
Unique Protocol Identification Number
NCT01073215
Brief Title
Primary Care Research Network for the Treatment of Adolescent Obesity
Acronym
TEENS
Official Title
Primary Care Research Network for the Treatment of Adolescent Obesity
Study Type
Interventional
2. Study Status
Record Verification Date
February 2012
Overall Recruitment Status
Completed
Study Start Date
July 2006 (undefined)
Primary Completion Date
May 2010 (Actual)
Study Completion Date
May 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Hospital of Philadelphia
Collaborators
Pennsylvania Department of Health, Geisinger Clinic, University of Pennsylvania
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The "Primary Care Research Network for the Treatment of Adolescent Obesity" will establish infrastructure within the primary care setting to support programmatic research on weight loss for underserved adolescents, primarily urban African Americans, rural Caucasians, and Latinos. Using primary care settings, to which many youths already have entry, may increase access for underserved adolescents to participate in obesity treatment and research. The primary project will be a 12 month randomized controlled study comparing the relative effectiveness of two interventions for weight reduction: Group Condition (a family based lifestyle modification program delivered by health care providers in 23 sessions); Self-Guided Condition (a family based lifestyle modification program that combines a self-guided, home-based approach with 6 sessions delivered by health care providers).
Detailed Description
The broad objective is to establish a Center of Excellence for Research on Obesity at The Children's Hospital of Philadelphia (CHOP) that will create a statewide, collaborative research network to develop and test effective treatments for reducing adolescent obesity and related medical co-morbidities in underserved populations. Collaborating institutions include Lincoln University (LU), Geisinger Health System (GHS), and the University of Pennsylvania (UPenn). Given the locations of these institutions, we will focus on urban African Americans and Latinos and rural Caucasian adolescents. The novelty of this program will be the use of a family-based, lifestyle modification program within the pediatric primary care setting with interdisciplinary teams trained to treat obese adolescents. Specific aims are to: a) design, implement, and evaluate improved treatments for obese teenagers, b) conduct focus groups and treatment development projects to better understand the needs of these populations and c) train, minority students and faculty to become healthcare research professionals. The primary research project will be a randomized clinical trial occurring at two sites: CHOP and GHS. In a four-year study, 156 adolescents (ages 12-16) will be randomized to either a one-year, 23 session, multi-family, group based Lifestyle Modification Program known as the Group Condition, or to a one-year, six-session Self-Guided Condition. Both Group and Self-Guided will be tested as possible treatment protocols for primary care pediatric practice.
The primary aim is to compare the effectiveness of these two treatments in reducing body mass index (BMI) at 12 months. Secondary aims will compare impact of the treatments on reduction of risk factors related to cardiovascular disease and diabetes, including lipids, glucose and insulin, waist circumference, blood pressure, and measures of appetite. Further, the effectiveness of these two treatments in reducing BMI at 15 and 18 months will also be analyzed. Training aims will be met through collaboration with Lincoln University to set up undergraduate summer internships, graduate assistantships, and faculty development. Other methods for achieving the objectives of the Center include: a) establishing a multidisciplinary advisory board consisting of parents, providers, and researchers; b) providing clinical training in obesity treatment for doctors, nurses, dieticians, and behavioral interventionists at our collaborating institutions (CHOP and GHS); c) making all protocols and materials culturally sensitive to the populations they serve; and d) carrying out treatment development activities to tailor the manuals for Latino youth and their families.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
Keywords
Adolescents, Obesity, Weight Management, Family-based Lifestyle Modification
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
173 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group Condition
Arm Type
Active Comparator
Arm Title
Self-Guided Condition
Arm Type
Experimental
Intervention Type
Behavioral
Intervention Name(s)
Family-Based Lifestyle Modification
Other Intervention Name(s)
TEENS Study
Intervention Description
The Self-Guided condition will receive the same manual content and recommendations for eating and physical activity as the Group Condition. Since this approach is primarily home-based, participants in this condition will also receive additional tips and guidelines to assist the family in following the program at home. There will be 6 visits with the health coach at weeks 01, 04, 08, 24, 40, and 52. Participants will receive 2 phone calls from health coach at weeks 16 and 32. Parents and teens will be encouraged to hold weekly meetings at home to discuss program goals and progress.
Intervention Type
Behavioral
Intervention Name(s)
Family-Based Lifestyle Modification Program
Other Intervention Name(s)
TEENS Study
Intervention Description
The Group condition will consist of a comprehensive family based lifestyle modification program of 23 visits (8 weekly, 8 bi-weekly, 7 monthly).
Intervention visits include a combination of 17 group sessions and 6 individual meetings with health coach. There will be 7 phone calls two weeks after each monthly visit. Adolescents and their parents attend concurrent group meetings. The content of the sessions will include topics related to nutrition, physical activity, and behavior modification for weight management.
Primary Outcome Measure Information:
Title
Percentage change in initial body mass index (BMI) at 12 months
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Compare mean reduction in percentage of initial BMI in the two treatments within each ethnic group/site (CHOP: urban African American adolescents and GHS: rural Caucasian adolescents
Time Frame
12 months
Title
Compare the effectiveness of the two treatment approaches on improving risk factors for cardiovascular disease and diabetes (Total, HDL, and LDL cholesterol, triglycerides, glucose, insulin, and blood pressure) and on improving liver function
Time Frame
12 months
Title
Compare mean reduction in percentage of initial BMI in each treatment group at month 6
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male or female adolescents
Age 12 to 16 years
Body Mass Index (BMI) of 28 kg/m2
Adolescent expresses desire to lose weight
Parent willing to participate
Live within 40 minutes from study clinic at CHOP or 60 minutes at Geisinger
Exclusion Criteria:
Uncontrolled hypertension (blood pressure > 140/90 mm HG)
Diabetes mellitus (fasting glucose > 126 mg/dl)
Any serious uncontrolled medical disorder that would complicate participation in a weight loss program
Bipolar disorder or psychosis (depression ok if adolescent is receiving treatment)
Use of any medication affecting body weight, appetite or metabolism within 30 days prior to the start of treatment
Positive pregnancy test at medical evaluation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert I Berkowitz, MD
Organizational Affiliation
Children's Hospital of Philadelphia and University of Pennsylvania
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Primary Care Research Network for the Treatment of Adolescent Obesity
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