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Remote Blood Pressure Monitoring for High Blood Pressure
N/A
Waitlist Available
Led By Catherine Sarkisian, MD, MSHS
Research Sponsored by University of California, Los Angeles
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Aged 18 years and older
Takes zero or three anti-hypertensive prescriptions (can include pills with 2 different drugs so could be on 2 medications)
Must not have
Other secondary causes of hypertension
Chronic kidney disease (CKD) Stage 3b (CrCL < 45) and above
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, six months
Awards & highlights
Summary
This trial is testing two ways to help people with hypertension monitor their blood pressure at home, to see if it can help lower blood pressure overall.
Who is the study for?
This trial is for adults with high blood pressure who use a non-connected blood pressure cuff at home, take up to three antihypertensive medications, and can access an online healthcare portal. They should have had two high BP readings in the last year and seen their primary care physician within that time. People with severe hypertension or certain health conditions like advanced kidney disease or recent heart problems cannot participate.Check my eligibility
What is being tested?
The study compares two remote monitoring methods for managing high blood pressure: one where patients manually record their BP and report it, versus another where the readings are automatically sent to their health system. The goal is to see which method better controls blood pressure across different University of California locations.See study design
What are the potential side effects?
Since this trial focuses on monitoring methods rather than medication changes, side effects are not a primary concern here. However, participants may experience stress or inconvenience related to using the technology or any potential technical issues.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 years old or older.
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I take up to three blood pressure medications.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have high blood pressure due to another health condition.
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My kidney function is reduced but not severely (Stage 3b or better).
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My thyroid condition is not under control.
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I have not had a heart attack or similar event in the last 3 months.
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I have a heart block or irregular heartbeat.
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I am not currently in hospice or receiving end-of-life care.
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I have been diagnosed with pheochromocytoma.
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I often have very low blood pressure.
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I have been diagnosed with severe narrowing of the aortic valve.
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I have a narrowed artery to my kidney.
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I have been diagnosed with Conn's syndrome.
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My kidneys are in the final stage of failure.
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I am already getting help for my high blood pressure from another service.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, six months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, six months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Continuous change in blood pressure (BP)
Secondary outcome measures
Body Weight Changes
Binary measure of controlled vs uncontrolled hypertension
Changes in blood pressure (BP) outcomes from integrated monitor readings
+1 moreOther outcome measures
Adverse events
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: IntegratedExperimental Treatment1 Intervention
Participants will have their home blood pressure readings sent directly to their participating health systems. Participants will also receive a wrap-around intervention.
Group II: ManualActive Control1 Intervention
Participants will record their own blood pressures and report them to their health care system as per usual care.
Find a Location
Who is running the clinical trial?
University of California, Los AngelesLead Sponsor
1,541 Previous Clinical Trials
10,266,383 Total Patients Enrolled
University of California Office of the President- Quality and Population Health ManagementUNKNOWN
University of California, DavisOTHER
919 Previous Clinical Trials
4,720,232 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have been diagnosed with high blood pressure in the last year.I have high blood pressure due to another health condition.My kidney function is reduced but not severely (Stage 3b or better).My thyroid condition is not under control.I have not had a heart attack or similar event in the last 3 months.I have a heart block or irregular heartbeat.I am 18 years old or older.I am willing and able to use a remote blood pressure monitor and a manual cuff at home, with help if needed.I take up to three blood pressure medications.I am not currently in hospice or receiving end-of-life care.I have been diagnosed with pheochromocytoma.I often have very low blood pressure.I have been diagnosed with severe narrowing of the aortic valve.I have a narrowed artery to my kidney.I have been diagnosed with Conn's syndrome.My kidneys are in the final stage of failure.I am already getting help for my high blood pressure from another service.I take one or no blood pressure medications.You need to have a blood pressure cuff at home that does not connect to an electronic medical record system.
Research Study Groups:
This trial has the following groups:- Group 1: Manual
- Group 2: Integrated
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
High Blood Pressure Patient Testimony for trial: Trial Name: NCT05390502 — N/A
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