Continuous Monitoring Using a Wearable Device Detects Activity‐Induced Heart Rate Changes After Administration of Amphetamine

Wearable digital devices offer potential advantages over traditional methods for the collection of health‐related information, including continuous collection of dense data while study subjects are ambulatory or in remote settings. We assessed the utility of collecting continuous actigraphy and card...

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Main Authors: Elena S. Izmailova, Ian L. McLean, Greg Hather, David Merberg, Jason Homsy, Matthew Cantor, Dmitri Volfson, Gaurav Bhatia, Eric D. Perakslis, Christopher Benko, John A. Wagner
Format: Article
Language:English
Published: Wiley 2019-11-01
Series:Clinical and Translational Science
Online Access:https://doi.org/10.1111/cts.12673
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spelling doaj-90670d7afa5640249e7ccb5cebc8272f2020-11-24T21:19:01ZengWileyClinical and Translational Science1752-80541752-80622019-11-0112667768610.1111/cts.12673Continuous Monitoring Using a Wearable Device Detects Activity‐Induced Heart Rate Changes After Administration of AmphetamineElena S. Izmailova0Ian L. McLean1Greg Hather2David Merberg3Jason Homsy4Matthew Cantor5Dmitri Volfson6Gaurav Bhatia7Eric D. Perakslis8Christopher Benko9John A. Wagner10Takeda Pharmaceuticals International, Inc. Cambridge Massachusetts USATakeda Pharmaceuticals International, Inc. Cambridge Massachusetts USATakeda Pharmaceuticals International, Inc. Cambridge Massachusetts USATakeda Pharmaceuticals International, Inc. Cambridge Massachusetts USATakeda Pharmaceuticals International, Inc. Cambridge Massachusetts USAKoneksa Health Inc. New York New York USATakeda Pharmaceuticals International, Inc. Cambridge Massachusetts USAKoneksa Health Inc. New York New York USATakeda Pharmaceuticals International, Inc. Cambridge Massachusetts USAKoneksa Health Inc. New York New York USATakeda Pharmaceuticals International, Inc. Cambridge Massachusetts USAWearable digital devices offer potential advantages over traditional methods for the collection of health‐related information, including continuous collection of dense data while study subjects are ambulatory or in remote settings. We assessed the utility of collecting continuous actigraphy and cardiac monitoring by deploying two US Food and Drug Administration (FDA) 510(k)‐cleared devices in a phase I clinical trial of a novel compound, which included the use of an amphetamine challenge. The Phillips Actiwatch Spectrum Pro (Actiwatch) was used to assess mobility and sleep. The Preventice BodyGuardian (BodyGuardian) was used for monitoring heart rate (HR) and respiratory rate (RR), via single‐lead electrocardiogram (ECG) recordings, together with physical activity. We measured data collection rates, compared device readouts with conventional measures, and monitored changes in HR measures during the amphetamine challenge. Completeness of data collection was good for the Actiwatch (96%) and lower for the BodyGuardian (80%). A good correlation was observed between device and in‐clinic measures for HR (r = 0.99; P < 0.001), but was poor for RR (r = 0.39; P = 0.004). Manual reviews of selected ECG strips corresponding to HR measures below, within, and above the normal range were consistent with BodyGuardian measurements. The BodyGuardian device detected clear HR responses after amphetamine administration while subjects were physically active, whereas conventional measures collected at predefined timepoints while subjects were resting and supine did not. Wearable digital technology shows promise for monitoring human subjects for physiologic changes and pharmacologic responses, although fit‐for‐purpose evaluation and validation continues to be important prior to the wider deployment of these devices.https://doi.org/10.1111/cts.12673
collection DOAJ
language English
format Article
sources DOAJ
author Elena S. Izmailova
Ian L. McLean
Greg Hather
David Merberg
Jason Homsy
Matthew Cantor
Dmitri Volfson
Gaurav Bhatia
Eric D. Perakslis
Christopher Benko
John A. Wagner
spellingShingle Elena S. Izmailova
Ian L. McLean
Greg Hather
David Merberg
Jason Homsy
Matthew Cantor
Dmitri Volfson
Gaurav Bhatia
Eric D. Perakslis
Christopher Benko
John A. Wagner
Continuous Monitoring Using a Wearable Device Detects Activity‐Induced Heart Rate Changes After Administration of Amphetamine
Clinical and Translational Science
author_facet Elena S. Izmailova
Ian L. McLean
Greg Hather
David Merberg
Jason Homsy
Matthew Cantor
Dmitri Volfson
Gaurav Bhatia
Eric D. Perakslis
Christopher Benko
John A. Wagner
author_sort Elena S. Izmailova
title Continuous Monitoring Using a Wearable Device Detects Activity‐Induced Heart Rate Changes After Administration of Amphetamine
title_short Continuous Monitoring Using a Wearable Device Detects Activity‐Induced Heart Rate Changes After Administration of Amphetamine
title_full Continuous Monitoring Using a Wearable Device Detects Activity‐Induced Heart Rate Changes After Administration of Amphetamine
title_fullStr Continuous Monitoring Using a Wearable Device Detects Activity‐Induced Heart Rate Changes After Administration of Amphetamine
title_full_unstemmed Continuous Monitoring Using a Wearable Device Detects Activity‐Induced Heart Rate Changes After Administration of Amphetamine
title_sort continuous monitoring using a wearable device detects activity‐induced heart rate changes after administration of amphetamine
publisher Wiley
series Clinical and Translational Science
issn 1752-8054
1752-8062
publishDate 2019-11-01
description Wearable digital devices offer potential advantages over traditional methods for the collection of health‐related information, including continuous collection of dense data while study subjects are ambulatory or in remote settings. We assessed the utility of collecting continuous actigraphy and cardiac monitoring by deploying two US Food and Drug Administration (FDA) 510(k)‐cleared devices in a phase I clinical trial of a novel compound, which included the use of an amphetamine challenge. The Phillips Actiwatch Spectrum Pro (Actiwatch) was used to assess mobility and sleep. The Preventice BodyGuardian (BodyGuardian) was used for monitoring heart rate (HR) and respiratory rate (RR), via single‐lead electrocardiogram (ECG) recordings, together with physical activity. We measured data collection rates, compared device readouts with conventional measures, and monitored changes in HR measures during the amphetamine challenge. Completeness of data collection was good for the Actiwatch (96%) and lower for the BodyGuardian (80%). A good correlation was observed between device and in‐clinic measures for HR (r = 0.99; P < 0.001), but was poor for RR (r = 0.39; P = 0.004). Manual reviews of selected ECG strips corresponding to HR measures below, within, and above the normal range were consistent with BodyGuardian measurements. The BodyGuardian device detected clear HR responses after amphetamine administration while subjects were physically active, whereas conventional measures collected at predefined timepoints while subjects were resting and supine did not. Wearable digital technology shows promise for monitoring human subjects for physiologic changes and pharmacologic responses, although fit‐for‐purpose evaluation and validation continues to be important prior to the wider deployment of these devices.
url https://doi.org/10.1111/cts.12673
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