IT-Supported Early Treatment Of Childhood Overweight
- Conditions
- Technology Based Obesity InterventionChildhood Obesity
- Registration Number
- NCT01188616
- Lead Sponsor
- Boston Medical Center
- Brief Summary
The goal of this exploratory/ developmental study is to develop and evaluate an integrated information system, Healthy Eating and Activity Today (HEAT), for promoting self-care in overweight children. HEAT is comprised of two components: 1)Telephone Linked Care-HEAT (TLC-HEAT), a self-care intervention delivered at home through totally automated telephone conversations; and 2) Primary Care-HEAT (PC-HEAT), a primary care intervention linked with TLC-HEAT and delivered through an electronic health record (EHR). The HEAT system will guide children in the early stages of overweight, i.e., children with Body Mass Index (BMI) 0-3 BMI points above the 95th percentile for age and gender, toward healthy weight management and assist the child's parent(s) and primary care provider (PCP) to support the child's efforts.
- Detailed Description
For this project we will: 1) develop TLC-HEAT for use by children in the earliest stage of overweight and their parents; 2) integrate TLC-HEAT with an electronic health record to provide child- and parent-reported behavior summaries combined with evidence-based decision support to primary care providers (PCPs) at the point-of-care (PC-HEAT); and 3) conduct a pilot study of the combined HEAT system to explore the appropriateness of conducting a larger, randomized clinical trial in the future.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- Not specified
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Children will be enrolled in the study if they meet a set of eligibility criteria which includes:
- 0-3 BMI points above the 95th %ile for age and gender
- age 9-12 years old
- a PCP at BMC
- an English speaking child and parent (based on interviewer assessment).
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Children will be considered ineligible for the study if they:
- have a health condition for which dietary recommendations in TLC-HEAT would be contraindicated
- have cognitive impairment (not in a mainstream academic class in school)
- have a terminal illness, current or former diagnosis of an eating disorder, or other diagnosis that the PCP deems should exclude them from participation
- plan to move away from the Boston area in less than 12 months
- are participating in another clinical weight treatment program.
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Initial screening will be done by research assistants over the phone.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Boston Medical Center
🇺🇸Boston, Massachusetts, United States