Utilizing Consumer Health Informatics to Support Management of Hypertension by Clinical Pharmacists in Primary Care

NCT ID: NCT02898584

Last Updated: 2020-07-14

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

16 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-10-31

Study Completion Date

2020-06-30

Brief Summary

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The purpose of this research study is to test the feasibility, acceptability, and preliminary effectiveness of the use of a mobile pharmacist-led intervention that incorporates home BP monitoring and medication reminders with patients recruited from a primary care setting, as well as identify challenges and potential solutions to broader implementation of a mobile pharmacist-led home-based BP monitoring intervention in primary care clinics through key stakeholder interviews.

Detailed Description

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Conditions

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Hypertension

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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BP Track

The study participants will be asked to monitor their blood pressure twice daily at home for twelve weeks, and sync the data to the mobile intervention so that a clinical pharmacist can review and incorporate the data into ongoing hypertension management.

Group Type OTHER

BP Track

Intervention Type OTHER

Interventions

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BP Track

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Have a smart phone compatible with mobile intervention
* Have been previously diagnosed with hypertension
* Have uncontrolled hypertension (systolic blood pressure \> 140 and/or diastolic blood pressure \> 90 on repeat measurement)
* Be under the care of a primary care physician at the recruitment clinic
* Be taking at least one antihypertensive medication
* Be English speaking

Exclusion Criteria

* Patients under the care of a clinical pharmacist for hypertension management, or under the care of a cardiologist
* Pregnant patients and anyone with the following unrelated, but serious medical conditions will also be excluded, as they may make blood pressure control difficult or necessitate frequent hospitalization: previous diagnosis of resistant hypertension; steroid dependent asthma or emphysema; cirrhosis or hepatic failure; stage C or D chronic heart failure; stage IV or V chronic kidney disease; and cancer (terminal or undergoing active chemotherapeutic or radiation therapy)
* Patients with other serious medical conditions (e.g., stroke, dementia) that may affect their ability to self-monitor blood pressure
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Michigan

OTHER

Sponsor Role lead

Responsible Party

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Lorraine Buis

Assistant Professor of Family Medicine, Medical School and Assistant Professor of Information, School of Information

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Lorraine R Buis, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Michigan

Locations

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University of Michigan

Ann Arbor, Michigan, United States

Site Status

Countries

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United States

References

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Buis LR, Roberson DN, Kadri R, Rockey NG, Plegue MA, Danak SU, Guetterman TC, Johnson MG, Choe HM, Richardson CR. Understanding the Feasibility, Acceptability, and Efficacy of a Clinical Pharmacist-led Mobile Approach (BPTrack) to Hypertension Management: Mixed Methods Pilot Study. J Med Internet Res. 2020 Aug 11;22(8):e19882. doi: 10.2196/19882.

Reference Type DERIVED
PMID: 32780026 (View on PubMed)

Buis LR, Roberson DN, Kadri R, Rockey NG, Plegue MA, Choe HM, Richardson CR. Utilizing Consumer Health Informatics to Support Management of Hypertension by Clinical Pharmacists in Primary Care: Study Protocol. JMIR Res Protoc. 2017 Oct 10;6(10):e193. doi: 10.2196/resprot.8059.

Reference Type DERIVED
PMID: 29017994 (View on PubMed)

Other Identifiers

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HUM00105772

Identifier Type: OTHER

Identifier Source: secondary_id

MICHR T3-RIP

Identifier Type: -

Identifier Source: org_study_id

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