Failure of Digital Device Performance in Monitoring Physical Exercise in a Pilot Study in Sedentary Persons with HIV

Author:

Bonato Matteo12ORCID,Marmondi Federica3ORCID,Turrini Filippo3,Albergoni Andrea4ORCID,Pennacchi Maddalena3,Cerizza Camilla3,Piacentini Maria Francesca5ORCID,Castagna Antonella3,Galli Laura3,Sartor Francesco67,Cinque Paola3

Affiliation:

1. Department of Biomedical Sciences for Health, Università degli Studi di Milano, 20133 Milan, Italy

2. IRCCS Istituto Ortopedico Galeazzi, Laboratory of Movement and Sport Sciences (LaMSS), 20157 Milan, Italy

3. Department of Infectious Diseases, IRCCS San Raffaele Scientific Institute, 20127 Milan, Italy

4. Department of Neuroscience Rehabilitation, Ophtalmology, Genetics and Maternal Child Health, Università degli Studi di Genova, 16148 Genua, Italy

5. Department of Movement, Human and Health Sciences, University of Rome ‘Foro Italico’, 00135 Rome, Italy

6. Department of Patient Care & Monitoring, Philips Research, 5656 AE Eindhoven, The Netherlands

7. School of Sport, Healthand Exercise Sciences, University of Wales, Bangor L57 2EF, UK

Abstract

Digital devices have gained popularity in the last 10 years as a tool for exercise prescription, the monitoring of daily physical activity, and nutrition for the management of a health-related parameter. Therefore, the aim of this study was to assess the effectiveness of the use of digital devices to monitor exercise data in sedentary persons with HIV who exercise following an individualized activity pacing (AP) protocol on cardiorespiratory fitness body composition, blood lipid profile, and psychological parameters. Twenty-four PLWH were enrolled in an 18-week randomized, open-label, pilot AP exercise protocol. All participants were monitored by a Health Band connected to a mobile app that transmitted the data to a server. At week 3, they were randomized either in an experimental group (EG), in which an open device configuration enabled them to receive training data feedback (n = 12), or continued with no data feedback (control group, n = 12). The primary endpoint was improvement from the baseline of 15% of steady-state oxygen consumption (V˙O2) during a 6-min walking test. Technical issues occurred when pairing the health band with the app, which prevented EG participants from regularly receiving data feedback, and with data transmission to the server, which enabled only 40% monitoring of the total training days. Consequently, the study outcomes could not be compared between the two groups, and participants also lost confidence in the study. However, 19 out of 24 participants completed the AP program. Overall, only 6 (32%) improved steady-state V˙O2, with no significant changes at W18 from the baseline. Significant reductions were observed of BMI (p = 0.040), hip circumference (p = 0.027), and total-(p = 0.049) and HDL-cholesterol (p = 0.045). The failure of digital device performance substantially affected study procedures, monitoring, and participants’ engagement, and likely limited the potential benefits of the AP exercise program.

Funder

Gilead Fellowship Program

Università degli Studi di Milano

Publisher

MDPI AG

Subject

Electrical and Electronic Engineering,Biochemistry,Instrumentation,Atomic and Molecular Physics, and Optics,Analytical Chemistry

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