Status:
COMPLETED
Reducing Disparities in Diabetes Risk Through Lifestyle Changes in Community Settings
Lead Sponsor:
University of California, San Francisco
Collaborating Sponsors:
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Conditions:
Diabetes
Eligibility:
All Genders
25+ years
Phase:
NA
Brief Summary
This study aims to design and test the effectiveness of a lifestyle diabetes risk reduction program, Live Well, Be Well, in reducing risk of diabetes in persons at risk with a focus on reaching lower-...
Detailed Description
To design and test the effectiveness of a lifestyle diabetes risk reduction program, Live Well, Be Well, to increase physical activity, decrease weight, and improve diet, offered in community-based se...
Eligibility Criteria
Inclusion
- age 25 and older
- moderate- to high-risk score on a Diabetes Risk Appraisal (DRA) (assessing sedentary behavior, family history of diabetes, race/ethnicity, gestational diabetes, hypertension, and high cholesterol) and a fasting fingerstick glucose level of 95-140 mg/dL (indicating high risk of diabetes).
- conversant in English or Spanish
Exclusion
- diabetes, assessed by self-report of having ever been told by a physician that they have diabetes (other than gestational) OR use of an oral hypoglycemic medication or insulin, OR a fingerstick fasting glucose level of \>150 mg/dl;
- unstable chronic or serious condition that could limit participation in unsupervised light to moderate physical activity (e.g. unstable angina, diagnosed with or hospitalized for chest pain, heart surgery, stroke, or myocardial infarction in the past 6 months);
- uncontrolled hypertension (systolic \>180 mmHg or diastolic \>105 mmHg);
- current pregnancy or attempting to conceive;
- plans to move from the area within 1 year;
- insufficient cognitive functioning to complete program procedures,
- implanted defibrillator,
- a hip or knee replacement in the past 3 months.
Key Trial Info
Start Date :
September 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2013
Estimated Enrollment :
230 Patients enrolled
Trial Details
Trial ID
NCT00770926
Start Date
September 1 2006
End Date
May 1 2013
Last Update
May 21 2013
Active Locations (1)
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1
University of California San Francisco
San Francisco, California, United States, 94118