Impact of Computerized Decision Support on Racial/Ethnic Disparities in Hypertension Outcomes

Sponsor
Brigham and Women's Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT01083940
Collaborator
Robert Wood Johnson Foundation (Other)
3,600
1
2
12
300.2

Study Details

Study Description

Brief Summary

In response to the Finding Answers: Disparities Research for Change call for proposals by the Robert Wood Johnson Foundation, we were funded to evaluate the effectiveness of a planned computerized decision support (CDS) intervention aimed at medical providers to overcome clinical inertia when treating blood pressure for hypertensive patients. Based on prior evaluation of the Brigham and Women's Hospital (BWH) adult primary care clinics, we hypothesize that racial and ethnic differences in blood pressure outcomes are largely attributable in differences in providers' aggressiveness in managing patients with hypertension based on patients' race and ethnicity. Within our network of 14 hospital and community-based Brigham and Women's Hospital adult primary care clinics, we aim to determine if the use of CDS to remind to medical providers of poorly controlled hypertensive patients to intensify their hypertension therapy will improve overall rates of blood pressure control and reduce the previously documented racial and ethnic disparities in blood pressure outcomes among our hypertensive patient population. Clinics will first be stratified by location (hospital-based versus community-based) and within each strata will be randomized to either have their providers receive CDS for hypertensive patients whose most recent blood pressure was uncontrolled or to usual care for hypertensive patients. More specifically, we will evaluate our planned intervention by utilizing an 18 month cluster-randomized controlled trial to examine the effectiveness the CDS for intensification of hypertension therapy in: improving levels of blood pressure control, improving provider adherence with recommended changes in drug therapy, and reducing racial/ethnic disparities in the processes of hypertension care and outcomes among our patients receiving primary care for a diagnosis of hypertension.

Condition or Disease Intervention/Treatment Phase
  • Other: Computerized reminders on hypertension intensification
Early Phase 1

Study Design

Study Type:
Interventional
Anticipated Enrollment :
3600 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Single (Participant)
Primary Purpose:
Health Services Research
Official Title:
Evaluating the Impact of Computerized Decision Support on Racial/Ethnic Disparities in Hypertension Outcomes
Study Start Date :
Oct 1, 2010
Anticipated Primary Completion Date :
Oct 1, 2011
Anticipated Study Completion Date :
Oct 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Experimental: Reminders to providers

Other: Computerized reminders on hypertension intensification
Reminder generated to prompt providers to intensify therapy when patient's blood pressure remains uncontrolled

No Intervention: usual care

Outcome Measures

Primary Outcome Measures

  1. Rate of blood pressure control at outcome between study arms [10/1/2010-10/1/2011]

Secondary Outcome Measures

  1. Rate of appropriate intensification of antihypertensive therapy [10/2010-7/2011]

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adult patients (> 20 years) with ICD-9 of hypertension with a minimum of 2 outpatient primary care visits in from 10/2008-10/2009 who receive care for hypertension in the outpatient practices at least once for hypertension from 10/2009-7/2001
Exclusion Criteria:
  • Pregnancy, age < 20 years, fewer than two hypertension-related visits from 10/2008-10/2009

Contacts and Locations

Locations

Site City State Country Postal Code
1 Brigham and Women's Hospital Boston Massachusetts United States 02120

Sponsors and Collaborators

  • Brigham and Women's Hospital
  • Robert Wood Johnson Foundation

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT01083940
Other Study ID Numbers:
  • 66708
First Posted:
Mar 10, 2010
Last Update Posted:
Jun 27, 2011
Last Verified:
Jun 1, 2011
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 27, 2011