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Clinical Trials/NCT01037920
NCT01037920
Completed
N/A

An Intervention to Improve Communication Between Physicians and Minority Patients With Hypertension

Denver Health and Hospital Authority1 site in 1 country179 target enrollmentJanuary 2010
ConditionsHypertension

Overview

Phase
N/A
Intervention
Not specified
Conditions
Hypertension
Sponsor
Denver Health and Hospital Authority
Enrollment
179
Locations
1
Primary Endpoint
medication adherence
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The objective of the project is a test-of-concept of an intervention to reduce the effects of the perception of discrimination on the care of patients with chronic illness. Perception of discrimination manifests itself as stereotype threat. We hypothesize that stereotype threat impairs communication between minority patients and their physicians because of increased stress and diminished trust, resulting in interactions that are less successful at enhancing patient self-efficacy, in turn resulting in lower rates of adherence with anti-hypertensive medication.

The intervention is a self-affirmation exercise performed prior to a patient-physician visit. A similar intervention has been shown to reduce the racial gap in academic performance in middle school classrooms.

We will explore the mechanistic effects of the intervention by analysis of audiotapes of patient-provider visits following the intervention. We will measure the effect of the intervention on minority hypertensive patients' adherence with antihypertensive medication and blood pressure.

We will enroll 200 African American and Latino patients with hypertension and randomize 100 patients to perform the exercise and 100 patients to perform a null control exercise before the visit. We will assess change in patient's adherence with antihypertensive medications and in blood pressure over the six months following the index visit. In order to better understand the effects of the intervention we will measure subject's mood following the exercise, and self-reported stress levels, trust in the physician, and medication self-efficacy following the visit. We will also assess the quality of the patient-provider interaction from detailed analysis of audiotapes and from patient questionnaires. Following a subsequent patient-physician visit, we will conduct telephone interviews with patients to assess for persistence of any effects of the intervention.

Registry
clinicaltrials.gov
Start Date
January 2010
End Date
December 2011
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • diagnosis of hypertension
  • age \> 21 years
  • use of Denver Health as their usual source of care and pharmacy services
  • self-described race/ethnicity of African American or Latino
  • ability to provide informed consent

Exclusion Criteria

  • pregnancy-related hypertension
  • end-stage renal disease
  • unable to speak or write English at at least a 6th grade level.

Outcomes

Primary Outcomes

medication adherence

Time Frame: 6 months

Secondary Outcomes

  • Blood pressure(3-6 months)

Study Sites (1)

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