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Clinical Trials/NCT03509506
NCT03509506CompletedNot Applicable

Usability and Effectiveness of a Self-care Mobile Health App in Individuals With Heart Failure

Texas Woman's University1 site in 1 country18 target enrollmentStarted: May 1, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
18
Locations
1
Primary Endpoint
Quality of Experience

Study Overview

Brief Summary

This study was designed to determine the potential benefits that individuals with heart failure (HF) could experience from using a mobile application.

Detailed Description

The mobile application is called the Heart Failure Health Storylines (HFHS). The potential benefits will be examined by determining the changes in physical activity and quality of life of the participants, who will use the application and compare the results with the participants, who will not use the application.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Adults with chronic heart failure, class I - III based on New York Heart Association (NYHA) scale
  • •Walking independently with/without an assistive device

Exclusion Criteria

  • •The participant will be excluded if one or more of the following is present
  • •Cognitive impairment (< 26 on Montreal Cognitive Assessment).
  • •Uncorrected vision
  • •Hearing problems
  • •Neurological disorders.
  • •Cannot speak and read the English language,
  • •Not owning a smart cell phone with internet access.

Arms & Interventions

Non-App Group

No Intervention

The participants will be instructed to continue their daily routine, track their daily steps with a pedometer, and record their daily steps on the "Activity Log" paper form.

App Group

Experimental

The participants will be trained how to use the mobile application (Heart Failure Health Storyline (HFHS)) to track their health status, physical activity, manage their medications schedule, and explore the other features that the application has. Additionally, they will receive a pedometer to track their daily steps and record their data on the mobile application.

Intervention: App Group (Behavioral)

Outcomes

Primary Outcomes

Quality of Experience

Time Frame: Change from baseline to 4 weeks

The Quality of Experience (QoE) survey will be used to measure the quality of experience in using the mobile application

Secondary Outcomes

  • Quality of Life for Individuals with Heart Failure(Change from baseline to 4 weeks)
  • Quality of Life for Individuals with HF(Change from baseline to 4 weeks)
  • Physical Activity will be indicated by daily step counts(Change from baseline to 4 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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