Achieving Blood Pressure Control Through Enhanced Discharge
This trial is active, not recruiting.
|Sponsor||Wayne State University|
|Collaborator||Blue Cross Blue Shield of Michigan Foundation|
|Start date||October 2013|
|End date||June 2015|
|Trial size||150 participants|
|Trial identifier||NCT02069015, BCBSMF 1956.11|
The primary aim of the study is to determine if enhanced discharge from the emergency department will improve blood pressure control and self-care management. Enhanced discharge will include a hypertension intervention delivered by a touch-screen kiosk over a three month period.
|Endpoint classification||efficacy study|
|Intervention model||parallel assignment|
Blood pressure control
time frame: Baseline to ninety days
Patient activation measure (PAM)
time frame: Baseline to 90 days
Male or female participants from 18 years up to 89 years old.
Inclusion Criteria: - Present with uncontrolled blood pressure to the emergency department (>140/90 for non-diabetics and >130/80 for diabetics) - Self-reported history of hypertension Exclusion Criteria: - End-stage renal disease - No history of hypertension - Do not present with uncontrolled blood pressure
|Official title||Achieving Blood Pressure Control Through Enhanced Discharge|
|Principal investigator||Julie A Gleason-Comstock, PhD|
|Description||A targeted sample of patients with uncontrolled blood pressure at the time of their emergency department visit discharge will be randomized into either standard or enhanced discharge. To control for medication effects in achieving blood pressure control, both groups will receive similar blood pressure medication while actively participating in the study.|
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