Improving Risk Factors for Diabetes Complications in Primary Care
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00482768|
Recruitment Status : Completed
First Posted : June 5, 2007
Last Update Posted : March 19, 2018
|Condition or disease||Intervention/treatment||Phase|
|Type 2 Diabetes||Behavioral: Practice Facilitation||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||2493 participants|
|Intervention Model:||Crossover Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Health Services Research|
|Official Title:||Improving Risk Factors for Diabetes Complications in Primary Care|
|Study Start Date :||June 2007|
|Actual Primary Completion Date :||April 2012|
|Actual Study Completion Date :||May 2013|
Intervention clinics will receive practice facilitation visits at regular intervals over a 12-month period.
Behavioral: Practice Facilitation
Clinics in the experimental arm will meet with a trained facilitator to work on change strategies that will improve risk factors for diabetes complications.
No Intervention: 2
Control clinics will deliver usual care for patients with diabetes.
- glycosylated hemoglobin [ Time Frame: 36 months ]
- systolic blood pressure [ Time Frame: 36 months ]
- LDL-cholesterol [ Time Frame: 36 months ]
- Change in risk of coronary heart disease [ Time Frame: 36 months ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00482768
|United States, Texas|
|University of Texas Health Sciences Center|
|San Antonio, Texas, United States, 78229-4404|
|Principal Investigator:||Polly H Noel, PhD||University of Texas Health Science Center-San Antonio|