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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
Children's Hospital of Philadelphia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring Adolescents, Obesity, Weight Management, Family-based Lifestyle Modification

Eligibility Criteria

12 Years - 16 Years (Child)All SexesDoes not accept healthy volunteers

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

    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
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    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

    We'll reach out to this number within 24 hrs