Mobile Health Management of Hypertension

NCT05856955 ยท Status: NOT_YET_RECRUITING ยท Phase: NA ยท Type: INTERVENTIONAL ยท Enrollment: 40

Last updated 2025-06-06

No results posted yet for this study

Summary

The investigators will pilot test a hypertension self-management intervention for feasibility and acceptability. The investigators will enroll adults (age โ‰ฅ18) with uncontrolled hypertension, identified from the electronic health record. In this feasibility trial, the research aim is to explore trial design, participant acceptability of the intervention and outcome measures, and to generate data to inform the design of a future randomized controlled trial.

Conditions

Interventions

BEHAVIORAL

mHealth Coaching Intervention

The intervention uses a mHealth virtual tool that facilitates human-device interaction and is delivered by smartphone application. The program has coaching and education components that lead to chronic disease behavior change. It has been previously validated to improve self-management, medication adherence, and quality of life in individuals with CVD. The participant engages by selecting responses on the touch screen. In this manner, participants converse with the coach, develop a therapeutic alliance, and record responses. The investigators will institute behavior change methodology to enhance intervention efficacy.

BEHAVIORAL

Enhanced Usual Care

Smart phone without health coach. A basic health application is installed on the smart phone provided to the participant.

Sponsors & Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

    collaborator NIH
  • University of Chicago

    lead OTHER

Principal Investigators

  • Amber Johnson, MD ยท University of Chicago

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2027-09-30
Primary Completion
2028-08-31
Completion
2028-11-30

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05856955 on ClinicalTrials.gov