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Impact of a Diabetes Risk Score on Lifestyle Education and Patient Adherence — IDEA  

Pre-diabetes Clinical Trial

Official title:
Impact of a Diabetes Risk Score on Lifestyle Education and Patient Adherence (IDEA Trial)

Clinical Trial Summary

The purpose of this randomized, controlled study is to evaluate whether the knowledge of a personalized diabetes risk score affects adherence to a 12-week diet and exercise lifestyle change program in prediabetic patients. The intervention group will receive diabetes risk score results at the beginning of the twelve weeks, and the control group will not receive these results. Both groups will review their baseline and 12-week diabetes risk score results at the conclusion of the program and will be followed for an additional twelve weeks. Attendance rates and changes in weight, BMI, abdominal circumference, blood pressure, HgA1c, fasting blood glucose, cholesterol, and diabetes risk score will be compared between the groups.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01932866
Study type Interventional
Source Wilford Hall Medical Center
Contact
Status Completed
Phase N/A
Start date June 2010
Completion date June 2013
View Details
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