Improving Blood Pressure Control in Stroke Patients by Increasing Access to a Home Blood Pressure Monitor

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to learn whether providing teaching with a low-cost device can help to improve blood pressure, health outcomes, patient self-efficacy without exacerbating inequity between advantaged and disadvantaged patients. The main question\[s\] it aims to answer are: 1. Does providing a free home blood pressure cuff improve control of hypertension? 2. Does providing a free home blood pressure cuff have a greater impact on control of hypertension in disadvantaged populations? 3. Does improved control of home blood pressure decrease adverse patient outcomes? Participants will be asked to * Take their blood pressure at home and records the results * Participate in follow-up phone calls from investigators at at 3 and 6 months Researchers will compare patients provided with home blood pressure monitors to those who are provided with routine education

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients over the age of 18 admitted to the Stanford Hospital (SHC) stroke service and discharging to home or acute rehab

• Diagnosis of Ischemic Stroke, Hemorrhagic Stroke, transient ischemic attack (TIA), or otherwise deemed to be at increased risk of stroke by the treating team (for example, asymptomatic carotid stenosis).

• No usable home blood pressure cuff available

• Diagnosis of hypertension or elevated blood pressure (\> 130/80) concerning to the treating clinician for hypertension

• Participant or surrogate able to apply a home blood pressure cuff on the participant

• Patient or Legally Authorized Representative (LAR) agree to participate and are able to consent.

Locations
United States
California
Stanford University Hospital
RECRUITING
Palo Alto
Time Frame
Start Date: 2023-05-01
Estimated Completion Date: 2025-04-30
Participants
Target number of participants: 50
Treatments
No_intervention: Standard of Care
Participants will receive routine stroke discharge education which is standard of care. A stroke nurse will provide and review with the patient a short informational pamphlet on the importance of blood pressure monitoring.
Experimental: Access to Blood Pressure Monitoring
Participants will also receive the teaching administered to the control group. In addition, they will be given an Omron Home Blood Pressure Cuff furnished by the study. The nurse will provide additional education on on how to use the cuff, and how to record values in a blood pressure log.
Related Therapeutic Areas
Sponsors
Leads: Stanford University

This content was sourced from clinicaltrials.gov