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Clinical Trials/NCT01040975
NCT01040975
Completed
N/A

Teen CHAT: Improving Physician Communication With Adolescents About Healthy Weight

Duke University1 site in 1 country684 target enrollmentSeptember 2009

Overview

Phase
N/A
Intervention
Not specified
Conditions
Communication
Sponsor
Duke University
Enrollment
684
Locations
1
Primary Endpoint
Physician communication
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to teach primary care physicians effective ways to counsel overweight and obese adolescent patients to attain a healthy weight. Fifty physicians and up to 660 adolescent patients from Duke University Health System (DUHS) Primary Care Clinics will take part in this study.

Patients will be identified by research study staff and asked if they would be willing to have their clinic visit audio recorded for research purposes. There are three phases of data collection. First, baseline encounters (n=200, 4 per physician) are audio recorded. Then, half of the physicians will be randomized to receive a tailored web-based intervention containing information about evidence-based techniques to help adolescents attain a healthy weight. A new set of 200 encounters (4 per physician) will be audio recorded. Then, all physicians will receive a Summary Report that outlines the adolescent's high risk behaviors that contribute to weight (sweetened beverages, fast food, breakfast, physical activity, screen time, and sleep) and a new set of 200 encounters will be audio recorded.

Data will be collected by trained data technicians, in-person and over the phone. Data is collected on laptop computers and then downloaded into password protected electronic files on a secure network server. All participants (adolescent patients and physicians) will be assigned a code number that is the sole identifier on all study data forms. Prior to and after coding, digital files will be stored in password protected directories to which only the data technicians and project manager have access. The web-based intervention will be password protected.

Registry
clinicaltrials.gov
Start Date
September 2009
End Date
February 2014
Last Updated
9 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Physician communication

Time Frame: after CD-ROM phase

Secondary Outcomes

  • Summary Report(After Summary Report Phase)
  • Adolescent Nutrition, Physical Activity, and BMI Z-score(3 months post-visit)

Study Sites (1)

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