Cardiovascular Diseases Clinical Trial
— H3Official title:
Midwest Small Practice Care Transformation Research Alliance (MSPCTRA)
NCT number | NCT02598284 |
Other study ID # | HS 023921-01 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | January 2016 |
Est. completion date | December 2018 |
Verified date | June 2019 |
Source | Northwestern University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study evaluates the ability of small primary care practices to 1) implement point-of-care and population management quality improvement strategies to improve cardiovascular quality of care (e.g., clinical decision support, patient education and counseling, or referral to smoking quit lines), and 2) implement the PopHealth performance measurement software to evaluate performance on the ABCS (aspirin when appropriate, blood pressure control, cholesterol management, and when applicable, smoking cessation) and allow regional benchmarking. This minimal risk study is a practice-randomized trial to determine a) whether point of care strategies improve ABCS performance measures compared to baseline, and b) whether adding locally tailored population management strategies to POC strategies improves performance on the ABCS measures more than POC strategies alone.
Status | Completed |
Enrollment | 226 |
Est. completion date | December 2018 |
Est. primary completion date | May 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 89 Years |
Eligibility |
Inclusion Criteria: - Providers practicing in Wisconsin, Illinois, and Indiana. - Practice is adult primary care-focused; [Further defined: health care organization dedicated to the provision of primary care, and a significant proportion of their patients are adults. Includes, but not limited to, family medicine, general internal medicine, general practice, geriatricians, nurse practitioners and physician assistants.] - Practice has 20 or fewer primary care providers; [Community health centers with 20 or fewer lead clinicians may be included; multi-specialty practices that provide primary care and have = 20 lead clinicians may be included.] - Providers must provide informed consent. Exclusion Criteria: - Non-English speaking providers |
Country | Name | City | State |
---|---|---|---|
United States | Northwestern University | Chicago | Illinois |
United States | Northern Illinois University (NIU) | DeKalb | Illinois |
United States | MetaStar | Madison | Wisconsin |
United States | Telligen | Oak Brook | Illinois |
United States | Purdue University | West Lafayette | Indiana |
Lead Sponsor | Collaborator |
---|---|
Northwestern University | Agency for Healthcare Research and Quality (AHRQ), Alliance of Chicago Community Health Services, American Medical Association, Illinois Department of Public Health, MetaStar, Inc., Northern Illinois University, Northwestern Medical Group, Purdue University, Telligen, Inc., University of Chicago |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in appropriate aspirin prescribing from baseline to 12 months | Measured using electronic health record data. Patients age = 18 with eligible encounters during measurement period (year prior and including measurement date) with IVD diagnosis on active problem list (on measurement date) or visit diagnosis (on or within 1 year prior to measurement date) who have aspirin prescribed. | 12 months | |
Primary | Change in clinical performance on blood pressure control from baseline to 12 months | Measured using electronic health record data. The proportion of adult (age 18-85) patients with hypertension with blood pressure <140/90 | 12 months | |
Primary | Change in clinical performance on cholesterol management from baseline to 12 months | Measured using electronic health record data. The proportion of adult patients who are eligible for statins with a stain prescription on active medication list. Eligible patients for this measure are (1) Patients age = 21 with an ASCVD diagnosis on problem list and (2) Patients age 40-75 with eligible encounters during the study period and diabetes on active problem list or as a visit diagnosis. | 12 months | |
Primary | Change in clinical performance on smoking cessation from baseline to 12 months | Measured using electronic health record data. The proportion of patients = 18 with eligible encounters during the study period who have an assessment of tobacco use recorded. Then, among patients who report using tobacco, the proportion who have received a tobacco cessation intervention. | 12 months | |
Secondary | Capacity for Quality Improvement | Collected via Change Process Capability Questionnaire (CPCQ) | 12 months |
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