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Research Articles

Small, slim, sleek, and familiar: user experiences with an ION wearable research alpha prototype transdermal alcohol monitor

ORCID Icon, , , ORCID Icon, , ORCID Icon & show all
Pages 186-191 | Received 07 Jul 2021, Accepted 16 Sep 2021, Published online: 07 Oct 2021
 

Abstract

Introduction

Transdermal alcohol monitors can help overcome issues with self-reporting in alcohol research and offer improvements over other biometric monitors as they provide passive and continuous measurement. The ION Wearable has recently entered the market by Milo Sensors; however, user acceptability has yet to be tested. This paper explores user experiences of an ION Wearable Research Alpha Prototype (ION RAP) monitor to determine if it is a feasible device for participant use in research studies.

Methods and materials

We undertook a qualitative study to explore user experiences of wearing an ION RAP monitor. We conducted semi-structured interviews with 23 participants after they wore an ION RAP for a 24-hour period. Participants were asked about first impressions of the device, physical comfortability, perceptions of the device, social experiences and drinking experiences. We used a deductive framework analysis.

Results

Overall, participants compared the ION RAP to a fitness watch, describing it as small, sleek, and familiar. Participants mostly reported positive physical and social experiences when wearing the ION RAP. Most participants did not feel that wearing the ION RAP impacted their drinking practices. Participants suggested that it would have greater utility if it were waterproof, and if issues with short battery life were resolved.

Conclusions

The ION RAP appears to be an acceptable alternative to traditional transdermal alcohol monitors. Future studies should examine acceptability in more diverse populations, including older adults. While user experience data is important, it is also vital that future studies examine its performance in measuring alcohol consumption.

Ethical approval

This study received ethics approval from the La Trobe Human Research Ethics Committee (HEC19249). Informed consent was obtained prior to participants entering the study.

Disclosure statement

No potential conflict of interest was reported by the authors.

Data availability statement

The data are not available as data sharing outside of the research team was not specified in the ethics approval.

Additional information

Funding

CW is funded by a National Health and Medical Research Council Early Career Fellowship. AP is supported by an Australian Research Council Discovery Early Career Researcher Award [DE190101074]. MM is funded by the Australian Government Research Training Program. The study was funded by a La Trobe University internal grant.

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