Evidence map›Paper›PMID 32519972›Full record

Trial reportJournal of medical Internet research2020

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

Mariska Weenk, Sebastian J Bredie, Mats Koeneman, Gijs Hesselink, Harry van Goor, Tom H van de Belt

2 registry-linked trialsOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of medical Internet research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 62 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 4 pooled it
16.9field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02933307 nacompletednot on this map

Continuous Monitoring of Vital Signs in Hospitalized Patients

TypeinterventionalSponsorRadboud University Medical CenterRan2015 to 2016Enrolled90ConditionsCarcinoma, Pancreatic Ductal, Colorectal Neoplasms, Arthritis, HypertensionArmsHealthPatch, ViSi Mobile
NCT04694599 naunknown statusnot on this mapstarted 2021, after this paper: background citation

The Effect of Continuous Pulse Oximetry Monitoring and Early Intervention Using Wearable Device on the Incidence of Postoperative Hypoxemia a Randomized Controlled Trial

TypeinterventionalSponsorSeoul National University HospitalRan2021 to 2021Enrolled94ConditionsPostoperative Respiratory ComplicationArmsLow flow oxygen
3 · Its place in the literature

Who cites it

62 citing papers in PubMed, 4 syntheses or guidelines pooled it, 149 citations in OpenAlex.

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2 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Mariska WeenkRadboud University Medical Center, Nijmegen, Netherlands.ORCID 0000-0002-0689-3669
Sebastian J BredieRadboud University Medical Center, Nijmegen, Netherlands.ORCID 0000-0002-6973-7540
Mats KoenemanRadboud University Medical Center, Nijmegen, Netherlands.ORCID 0000-0001-7336-7135
Gijs HesselinkRadboud University Medical Center, Nijmegen, Netherlands.ORCID 0000-0003-2532-0724
Harry van GoorRadboud University Medical Center, Nijmegen, Netherlands.ORCID 0000-0003-0323-4876
Tom H van de BeltRadboud University Medical Center, Nijmegen, Netherlands.ORCID 0000-0002-5401-8973
Radboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWearable 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.

objectiveThis 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).

methodsIn 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.

resultsA 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.

conclusionsBoth 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 registrationClinicaltrials.gov NCT02933307; http://clinicaltrials.gov/ct2/show/NCT02933307.

Indexed as

AdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedMonitoring, PhysiologicSurveys and QuestionnairesVital SignsWearable Electronic Devicescontinuous monitoringdigital healthremote monitoringremote sensing technologyvital signswearable electronic deviceswireless technology

Identifiers

PMID32519972
PMCPMC7315364
OpenAlexW3002214654

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.