Reducing Clinical Inertia in Hypertension Treatment: A Pragmatic Trial
- Conditions
- Hypertension
- Interventions
- Other: Active Outreach to Patients and Providers
- Registration Number
- NCT01145391
- Lead Sponsor
- University of Colorado, Denver
- Brief Summary
The goal of this project is to use health information technology and team-based care in novel ways to support the establishment of a Patient-Centered Medical Home model of care aimed at improving the diagnosis and management of hypertension. Compared with patients who receive usual care, patients who receive intervention will have a lower average systolic blood pressure 9 months after randomization.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 591
- Adult men and women age 18-79
- At least 2 Blood Pressure readings from separate days on record
- Average of last 3 Blood Pressure readings (or last 2 if only 2 available) with (Systolic Blood Pressure ≥140 or Diastolic Blood Pressure ≥90) and (last Systolic Blood Pressure ≥135 or last Diastolic Blood Pressure ≥85), recorded by any University of Colorado Hospital clinic within the last 18 months
- No clinic visit in the past month
- At least one Primary Care Physician visit in the past 18 months
- First Primary Care Physician visit at least 6 months in the past
- Serious comorbidities, including active cancer diagnosis, hospice care, nursing home residence
- Diagnosis of diabetes (these patients are enrolled in a separate study that also targets Blood Pressure control)
- End-stage renal disease / hemodialysis
- Primary Care Physician appointment pending
- Patient instructed to monitor Blood Pressure at home / documentation of white coat hypertension
- Blood Pressure managed by specialist or outside provider
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intervention Active Outreach to Patients and Providers An outreach coordinator raised patient and provider awareness of unmet Blood Pressure goals, arranged Blood Pressure-focused clinic visits, and furnished providers with treatment decision support.
- Primary Outcome Measures
Name Time Method Blood Pressure Baseline, 9 months Hypothesis: compared with patients who receive usual care, patients who receive intervention will have an average systolic blood pressure that is at least 5 points lower 9 months after randomization.
- Secondary Outcome Measures
Name Time Method Clinical Inertia Baseline, 9 months Definition of clinical inertia: failure of a primary care physician to initiate/intensify anti-hypertensive medications AND the failure to provide behavioral counseling to lower blood pressure during a clinic visit where blood pressure is elevated above 140/90 mm Hg. The clinical inertia measure is the percentage of clinic visits with clinical inertia present divided by the total number of clinic visits.
We report a change in group mean levels of clinical inertia from baseline to 9 months post-randomization. Negative values for clinical inertia represent a decrease in the percentage of clinic visits where clinical inertia was present. Pre-randomization clinical inertia was assessed in the last 2 clinic visits prior to randomization, and post-randomization inertia was assessed in the first 2 post-randomization visits.
Hypothesis: clinical inertia will be significantly greater in the usual care compared with intervention group in the post-randomization period.
Trial Locations
- Locations (1)
University of Colorado Denver
🇺🇸Aurora, Colorado, United States