Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
62 participants
INTERVENTIONAL
2018-09-21
2019-08-30
Brief Summary
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Detailed Description
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Home BP monitoring (HBPM) is a promising solution to catalyze patient engagement in self-management while offering clinicians reliable and up-to-date data, thereby improving clinical management. Home blood pressure monitoring (HBPM) is now widely recommended as an effective additional tool for improved hypertension management, however broad implementation has not occurred. The convenience of mobile phones has led to high and increasing ownership among all age groups, thus there is great potential to leverage mobile health (mHealth) applications to make HBPM easy, convenient, and even more helpful for both clinicians and patients.
Based upon extensive stakeholder input, the investigators' multidisciplinary team designed a comprehensive mobile phone supported HBPM system called MyBP. MyBP efficiently educates patients via professionally-developed videos and supports bi-weekly BP self-monitoring with recurring feedback using proactive, bidirectional automated texting. Prior pilot testing at three unique clinical sites with middle-aged adults (mean 50 y/o) suggests good usability and positive effects on self-management behaviors. High priority next steps are to: 1) test MyBP specifically with older adults (and caregivers) to fully understand their unique experiences in regards to HBPM via mobile phone, and 2) explore how best to share MyBP data with primary care providers (PCPs). Therefore, the aims of this study are to:
1. Collect pilot data on longitudinal usage of MyBP and BP reduction over 6-9 months within an older adult population.
2. Examine factors influencing adoption and sustained use of MyBP and any associated BP reduction.
3. Identify potentially unique user experiences among older adults with increasing frailty and in those who rely on caregivers.
Methods. Forty-eight older adults (60-85 y/o) with uncontrolled hypertension will be randomized 2:1 to active intervention (MyBP plus a home BP cuff) or usual care (home BP cuff alone) for 6-9 months. Participants will be recruited from UPMC primary care practices. For participants for whom a caregiver has primary responsibility for hypertension-related health behaviors, MyBP will be used by the caregiver. Gait speed will be measured to assess frailty. At baseline and study completion, standardized measurement of home BP will be conducted. Patients and caregivers will complete questionnaires and a semi-structured audio-recorded interview to assess factors associated with MyBP utility and engagement, BP self-management and BP lowering.
Future use of data. Findings will be used to refine the MyBP system design to best fit the target audience and as "preliminary evidence" in an NIH R01 proposal to test in a randomized clinical trial of MyBP in the primary care setting among both mid-life and older adults with uncontrolled hypertension.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
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Enhanced usual care
Participants receive a personal, validated home BP monitor with oral and written instruction.
Personal BP monitor
Battery-powered BP monitor for personal use
MyBP
Participants receive a personal, validated home BP monitor with oral and written instruction. In addition patients receive instruction on, and access to, MyBP. This program provides high BP education through online videos and automated, bidirectional text messaging to assist in continuous home BP self-monitoring.
MyBP
This program includes online video high BP education and longitudinal, personalized assistance of home BP self-monitoring.
Personal BP monitor
Battery-powered BP monitor for personal use
Interventions
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MyBP
This program includes online video high BP education and longitudinal, personalized assistance of home BP self-monitoring.
Personal BP monitor
Battery-powered BP monitor for personal use
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Office systolic BP reading 150 mm Hg or higher
* Owns a cell phone with unlimited texting
Exclusion Criteria
* Dementia
55 Years
ALL
No
Sponsors
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University of Pittsburgh
OTHER
Responsible Party
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Matthew Muldoon
Professor
Principal Investigators
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Matthew F Muldoon, MD
Role: PRINCIPAL_INVESTIGATOR
University of Pittsburgh
Locations
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University of Pittsburgh
Pittsburgh, Pennsylvania, United States
Countries
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References
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Einhorn J, Murphy AR, Rogal SS, Suffoletto B, Irizarry T, Rollman BL, Forman DE, Muldoon MF. Automated Messaging Program to Facilitate Systematic Home Blood Pressure Monitoring: Qualitative Analysis of Provider Interviews. JMIR Cardio. 2023 Dec 4;7:e51316. doi: 10.2196/51316.
Other Identifiers
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PRO18050328
Identifier Type: -
Identifier Source: org_study_id
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