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Impact of a Diabetes Risk Score on Lifestyle Education and Patient Adherence (IDEA Trial)
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.
Age
30 - 75 years
Sex
ALL
Healthy Volunteers
No
David Grant Medical Center
Travis AFB, California, United States
Andrews Military Medical Center
Andrews Air Force Base Census Designated Place, Maryland, United States
Nellis Family Medicine
Nellis Air Force Base, Nevada, United States
Wright Patterson Medical Center
Wright-Patterson AFB, Ohio, United States
Wilford Hall Ambulatory Surgical Center
Lackland Air Force Base, Texas, United States
Start Date
June 1, 2010
Primary Completion Date
June 1, 2013
Completion Date
June 1, 2013
Last Updated
August 30, 2013
223
ACTUAL participants
diabetic risk score
OTHER
Lead Sponsor
59th Medical Wing
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05041491