3.8 Article

Home-Based Spirometry Telemonitoring After Allogeneic Hematopoietic Cell Transplantation: Mixed Methods Evaluation of Acceptability and Usability

Journal

JMIR FORMATIVE RESEARCH
Volume 6, Issue 2, Pages -

Publisher

JMIR PUBLICATIONS, INC
DOI: 10.2196/29393

Keywords

allogeneic hematopoietic cell transplantation; home-based spirometry; acceptability; usability; mixed methods evaluation; patient perspectives; spirometry; feasibility; mHealth; home-based; remote care; respirology; pulmonary medicine; mobile phone

Funding

  1. National Institutes of Health/National Institute of Allergy and Infectious Diseases [K23 AI117024]
  2. National Cancer Institute (Cancer Center Support Grant) at the National Institutes of Health [P30 CA016672]

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This study aimed to investigate the usability and acceptability of home-based spirometry (HS) among recipients of allogeneic hematopoietic cell transplant (AHCT). The results showed that participants found HS to be highly acceptable and helpful in managing AHCT-related symptoms, as well as detecting health-related problems early. The study concluded that HS is easy to use with no significant barriers from the patient's perspective.
Background: Home-based spirometry (HS) allows for the early detection of lung complications in recipients of an allogeneic hematopoietic cell transplant (AHCT). Although the usability and acceptability of HS are critical for adherence, patient-reported outcomes of HS use remain poorly understood in this setting. Objective: The aim of this study is to design a longitudinal, mixed methods study to understand the usability and acceptability of HS among recipients of AHCT. Methods: Study participants performed HS using a Bluetooth-capable spirometer that transmitted spirometry data to the study team in real time. In addition, participants completed usability questionnaires and in-depth interviews and reported their experiences with HS. Analysis of interview data was guided by the constructs of performance expectancy, effort expectancy, and social influence from the Unified Theory of Acceptance and Use of Technology model. Results: Recipients of AHCT found HS to be highly acceptable despite modest technological barriers. On average, participants believed that the HS was helpful in managing symptoms related to AHCT (scores ranging from 2.22 to 2.68 on a scale of 0-4) and for early detection of health-related problems (score range: 2.88-3.12). Participants viewed HS favorably and were generally supportive of continued use. No significant barriers to implementation were identified from the patient's perspective. Age and gender were not associated with the patient perception of HS. Conclusions: Study participants found HS acceptable and easy to use. Some modifiable technical barriers to performing HS were identified; however, wider implementation of pulmonary screening is feasible from the patient's perspective.

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