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Continuous Monitoring of Vital Signs in the General Ward Using Wearable Devices: Randomized Controlled Trial

BACKGROUND: Wearable devices can be used for continuous patient monitoring in the general ward, increasing patient safety. Little is known about the experiences and expectations of patients and health care professionals regarding continuous monitoring with these devices. OBJECTIVE: This study aimed...

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Autores principales: Weenk, Mariska, Bredie, Sebastian J, Koeneman, Mats, Hesselink, Gijs, van Goor, Harry, van de Belt, Tom H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JMIR Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315364/
https://www.ncbi.nlm.nih.gov/pubmed/32519972
http://dx.doi.org/10.2196/15471
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author Weenk, Mariska
Bredie, Sebastian J
Koeneman, Mats
Hesselink, Gijs
van Goor, Harry
van de Belt, Tom H
author_facet Weenk, Mariska
Bredie, Sebastian J
Koeneman, Mats
Hesselink, Gijs
van Goor, Harry
van de Belt, Tom H
author_sort Weenk, Mariska
collection PubMed
description BACKGROUND: Wearable devices can be used for continuous patient monitoring in the general ward, increasing patient safety. Little is known about the experiences and expectations of patients and health care professionals regarding continuous monitoring with these devices. OBJECTIVE: This study aimed to identify positive and negative effects as well as barriers and facilitators for the use of two wearable devices: ViSi Mobile (VM) and HealthPatch (HP). METHODS: In this randomized controlled trial, 90 patients admitted to the internal medicine and surgical wards of a university hospital in the Netherlands were randomly assigned to continuous vital sign monitoring using VM or HP and a control group. Users’ experiences and expectations were addressed using semistructured interviews. Nurses, physician assistants, and medical doctors were also interviewed. Interviews were analyzed using thematic content analysis. Psychological distress was assessed using the State Trait Anxiety Inventory and the Pain Catastrophizing Scale. The System Usability Scale was used to assess the usability of both devices. RESULTS: A total of 60 patients, 20 nurses, 3 physician assistants, and 6 medical doctors were interviewed. We identified 47 positive and 30 negative effects and 19 facilitators and 36 barriers for the use of VM and HP. Frequently mentioned topics included earlier identification of clinical deterioration, increased feelings of safety, and VM lines and electrodes. No differences related to psychological distress and usability were found between randomization groups or devices. CONCLUSIONS: Both devices were well received by most patients and health care professionals, and the majority of them encouraged the idea of monitoring vital signs continuously in the general ward. This comprehensive overview of barriers and facilitators of using wireless devices may serve as a guide for future researchers, developers, and health care institutions that consider implementing continuous monitoring in the ward. TRIAL REGISTRATION: Clinicaltrials.gov NCT02933307; http://clinicaltrials.gov/ct2/show/NCT02933307.
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spelling pubmed-73153642020-07-01 Continuous Monitoring of Vital Signs in the General Ward Using Wearable Devices: Randomized Controlled Trial Weenk, Mariska Bredie, Sebastian J Koeneman, Mats Hesselink, Gijs van Goor, Harry van de Belt, Tom H J Med Internet Res Original Paper BACKGROUND: Wearable devices can be used for continuous patient monitoring in the general ward, increasing patient safety. Little is known about the experiences and expectations of patients and health care professionals regarding continuous monitoring with these devices. OBJECTIVE: This study aimed to identify positive and negative effects as well as barriers and facilitators for the use of two wearable devices: ViSi Mobile (VM) and HealthPatch (HP). METHODS: In this randomized controlled trial, 90 patients admitted to the internal medicine and surgical wards of a university hospital in the Netherlands were randomly assigned to continuous vital sign monitoring using VM or HP and a control group. Users’ experiences and expectations were addressed using semistructured interviews. Nurses, physician assistants, and medical doctors were also interviewed. Interviews were analyzed using thematic content analysis. Psychological distress was assessed using the State Trait Anxiety Inventory and the Pain Catastrophizing Scale. The System Usability Scale was used to assess the usability of both devices. RESULTS: A total of 60 patients, 20 nurses, 3 physician assistants, and 6 medical doctors were interviewed. We identified 47 positive and 30 negative effects and 19 facilitators and 36 barriers for the use of VM and HP. Frequently mentioned topics included earlier identification of clinical deterioration, increased feelings of safety, and VM lines and electrodes. No differences related to psychological distress and usability were found between randomization groups or devices. CONCLUSIONS: Both devices were well received by most patients and health care professionals, and the majority of them encouraged the idea of monitoring vital signs continuously in the general ward. This comprehensive overview of barriers and facilitators of using wireless devices may serve as a guide for future researchers, developers, and health care institutions that consider implementing continuous monitoring in the ward. TRIAL REGISTRATION: Clinicaltrials.gov NCT02933307; http://clinicaltrials.gov/ct2/show/NCT02933307. JMIR Publications 2020-06-10 /pmc/articles/PMC7315364/ /pubmed/32519972 http://dx.doi.org/10.2196/15471 Text en ©Mariska Weenk, Sebastian J Bredie, Mats Koeneman, Gijs Hesselink, Harry van Goor, Tom H van de Belt. Originally published in the Journal of Medical Internet Research (http://www.jmir.org), 10.06.2020. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in the Journal of Medical Internet Research, is properly cited. The complete bibliographic information, a link to the original publication on http://www.jmir.org/, as well as this copyright and license information must be included.
spellingShingle Original Paper
Weenk, Mariska
Bredie, Sebastian J
Koeneman, Mats
Hesselink, Gijs
van Goor, Harry
van de Belt, Tom H
Continuous Monitoring of Vital Signs in the General Ward Using Wearable Devices: Randomized Controlled Trial
title Continuous Monitoring of Vital Signs in the General Ward Using Wearable Devices: Randomized Controlled Trial
title_full Continuous Monitoring of Vital Signs in the General Ward Using Wearable Devices: Randomized Controlled Trial
title_fullStr Continuous Monitoring of Vital Signs in the General Ward Using Wearable Devices: Randomized Controlled Trial
title_full_unstemmed Continuous Monitoring of Vital Signs in the General Ward Using Wearable Devices: Randomized Controlled Trial
title_short Continuous Monitoring of Vital Signs in the General Ward Using Wearable Devices: Randomized Controlled Trial
title_sort continuous monitoring of vital signs in the general ward using wearable devices: randomized controlled trial
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315364/
https://www.ncbi.nlm.nih.gov/pubmed/32519972
http://dx.doi.org/10.2196/15471
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