Effectiveness of BP Remote Monitoring With Virtual Physician Management in Hypertensive Patients.
Status unconfirmed · Not applicable
Conditions studied: Hypertension, Stroke (CVA) or TIA
In brief
To assess the feasibility and adoptability of DailyDoctor's remote monitoring clinical decision support software tool in helping physicians virtually manage systolic blood pressures among patients with history of stroke or TIA to a target systolic blood pressure (\<140 mmHg or a lower target range specified by referring physicians) using remote monitoring and independent clinical judgement.
Key facts
- Study ID
- NCT05319418
- Run by
- AIRx Health, Inc.
- People needed
- 50
- Starts
- 2022-04-01
- Expected to finish
- 2023-03-01
- Last updated by the study team
- 2022-04-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age 18 years or older. A history of ischemic or hemorrhagic stroke, or transient ischemic attack. The ability to report blood pressure values by phone (either a patient or designated caregiver may call to report values).
- At least 2 BP measurements that are ≥140 mmHg systolic or ≥90 mmHg diastolic obtained on different days in the last 6 months in any setting (including at home, in clinic, or in the hospital setting).
- The referring physician feels the patient would benefit from BP optimization. Consent to receive care from telehealth physicians available through the DailyDoctor monitoring platform.
- English or Spanish speaking.
You may not qualify if…
- Currently enrolled in another interventional research study Inability to comply with study protocol Have a planned surgical procedure during the study period Upper arm circumference > 20 inches Has diagnosis of end-stage renal disease (GFR < 15 mL/min), Serum creatinine > 2.0 mg/dL (176.8 μmol/L), or currently undergoing dialysis treatment (10) Women who are pregnant or who are planning to become pregnant during the study period.
- Blood pressure reduction is not indicated (e.g. patients who have a high blood pressure target to augment cerebral perfusion).
- Any other reason that, in the opinion of the investigator, makes the person a poor candidate for participation in this study
Where it is running
- Stanford Stroke Center — Stanford, California, United States
Full record on ClinicalTrials.gov
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