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N/A Completed N=139 Randomized Prevention

Achieving Blood Pressure Control Through Enhanced Discharge

Source: ClinicalTrials.gov NCT02069015 ↗
Enrolled (actual)
139
Serious AEs
0.0%
Results posted
Dec 2020
Primary outcomePrimary: Blood Pressure (Systolic) at 180 Days — 131; 131 mmHg — p=<0.001

Summary

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.

Outcome Measures

OutcomeResultp-value
PRIMARY
Blood Pressure (Systolic) at 180 Days
131; 131 <0.001 sig
SECONDARY
Patient Activation Measure (PAM)
3; 19; 34; 7; 7; 20

Eligibility Criteria

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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02069015). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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