CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 49 enrolled
Drug / intervention
Skyn Monitor Lab Session 1 +2 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03617705
NCT03617705N/ACompleted

Laboratory and Field Validation of a Wrist-Worn Alcohol Monitor

University of Florida·interventional·Posted Aug 6, 2018·Updated Jun 28, 2023

In Brief

A clinical study evaluating Skyn Monitor Lab Session 1, Skyn Monitor Field Test with EMA App, and 1 other intervention for Human Immunodeficiency Virus (HIV). Completed, enrolled 49 participants across 2 sites.

Detailed Summary

This study will validate a wrist-worn alcohol monitor (BACtrack Skyn) in both laboratory and real-life settings.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedAug 6, 2018
Enrollment StartApr 1, 2019
Primary CompletionJun 30, 2022
TodayJul 2, 2026
Enrollment to primary: 3.2 yearsPosted 7.9 years ago

Interventions

Skyn Monitor Lab Session 1device

Participants will be instructed to wear the Skyn wrist-worn alcohol monitor and drink 3 beers over the course of an hour and a half. BrAC will be measured every 15 minutes throughout the session.

Skyn Monitor Field Test with EMA Appdevice

After Skyn Monitor Lab Session 1, participants will be instructed to wear Skyn monitor for the rest of the day and the following two weeks. Participants will also enter information on each drinking session during the two week time using a mobile-based ecological momentary assessment (EMA) to collect real-time data in daily life.

Skyn Monitor Lab Session 2device

Participants will be instructed to wear the Skyn wrist-worn alcohol monitor and drink 3 beers over the course of an hour and a half. BrAC will be measured every 15 minutes throughout the session. Participant will also complete device acceptability and usability survey.