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Mobile Health Program for High Blood Pressure
N/A
Recruiting
Research Sponsored by University of Pittsburgh
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Prescribed use of one or more antihypertensive agents as identified by the International Society of Hypertension core drug-treatment strategy
Be older than 18 years old
Must not have
Planned major surgery, cardiovascular or non-cardiovascular
Heart failure necessitating hospital admission ≤3 months prior to study inclusion
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 12 months
Awards & highlights
No Placebo-Only Group
Summary
This trial will test a home-based blood pressure monitoring program with health education and coaching to see if it can help reduce cardiovascular disease in rural populations.
Who is the study for?
This trial is for rural residents with uncontrolled high blood pressure who are on hypertension medication and can use a smartphone. They must speak English well enough for the study, not be pregnant or planning pregnancy soon, and not have severe health issues like recent heart failure or life-threatening conditions.
What is being tested?
The study tests a home-based blood pressure monitoring program against regular monitoring plus WebMD app usage. It aims to see if personalized coaching and education help manage hypertension better in rural areas.
What are the potential side effects?
Since this trial involves non-drug interventions like using an app and monitoring devices, side effects may include discomfort from frequent blood pressure checking or stress from self-management of health data.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am taking medication for high blood pressure.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am scheduled for a major surgery soon.
Select...
I was hospitalized for heart failure within the last 3 months.
Select...
I have not had a heart attack or severe chest pain in the last 3 months.
Select...
I do not have a non-heart related condition expected to be fatal within a year.
Select...
I understand the study's requirements and passed the consent quiz.
Select...
I have had very high blood pressure (over 200/120 mm Hg).
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 12 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in systolic and diastolic blood pressure from baseline to 6 months
Secondary study objectives
Adherence to antihypertensive medications
Patient-Reported Outcomes
Pharmaceutical Preparations
+1 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: InterventionExperimental Treatment2 Interventions
A smartphone-based, interactive coaching application designed to enhance adherence to home-based blood pressure monitoring, provided guidance on blood pressure management, patient-facing education, and assistance with modifying behaviors associated with poor blood pressure control; connected to a wireless blood pressure cuff for accurate blood pressure measurement and automated storage on a digital platform. All participants in the experimental arm receive a smartphone for the 6-month intervention duration and the home-based blood pressure cuff.
Group II: Enhanced usual careActive Control2 Interventions
WebMD, a smartphone-based tool for learning about blood pressure and other health conditions. Enhanced usual care participants receive a wireless blood pressure cuff for accurate blood pressure measurement and automated storage on a digital platform. All participants in the experimental arm receive a smartphone for the 6-month intervention duration and the home-based blood pressure cuff.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for high blood pressure include ACE inhibitors and ARBs, which relax blood vessels by inhibiting the renin-angiotensin system; calcium channel blockers, which prevent calcium from entering heart and blood vessel cells, leading to relaxed vessels; diuretics, which help the kidneys remove excess sodium and water, reducing blood volume; and beta-blockers, which reduce heart rate and the force of contraction. Understanding these mechanisms is crucial for patients as it helps tailor treatment plans to individual needs, ensuring effective blood pressure control and minimizing side effects, especially when combined with continuous monitoring and personalized coaching.
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Who is running the clinical trial?
University of PittsburghLead Sponsor
1,787 Previous Clinical Trials
16,359,019 Total Patients Enrolled
National Heart, Lung, and Blood Institute (NHLBI)NIH
3,929 Previous Clinical Trials
47,764,896 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I am scheduled for a major surgery soon.I was hospitalized for heart failure within the last 3 months.You live in one of the 48 counties considered rural by the Center for Rural Pennsylvania.I understand the study's requirements and passed the consent quiz.I have not had a heart attack or severe chest pain in the last 3 months.I have high blood pressure that's not well-controlled, with specific readings on two visits.I do not have a non-heart related condition expected to be fatal within a year.I have had very high blood pressure (over 200/120 mm Hg).I am taking medication for high blood pressure.
Research Study Groups:
This trial has the following groups:- Group 1: Intervention
- Group 2: Enhanced usual care
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.
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