Clinical Trials Directory

Trials / Completed

CompletedNCT05186233

Use of Consumer Sleep Technology to Treat Shift Work Disorder

Innovations in Wearable Technology for Correcting Circadian Misalignment in Shift Work Disorder

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
63 (actual)
Sponsor
Henry Ford Health System · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to examine the effectiveness of a personalized light exposure schedule for Shift Work Disorder (SWD) in night shift workers compared to a non-personalized light exposure schedule.

Detailed description

Participants will be randomized into each condition (n = 25) in a 1:1 ratio. Variables of interest, dim light melatonin onset (DLMO) and shift work disorder (SWD) symptoms, will be assessed before and after the intervention, which will last two weeks. All participants (N=50) will be asked to wear an Apple Watch for two weeks leading up to an in-lab visit. Activity data collection from the Apple Watch will be processed through a mathematical model of the human circadian pacemaker (previously validated in SWD) to generate estimates of DLMO. This two-week period is followed by a 27-hour laboratory visit for pre-treatment assessment of DLMO (hourly saliva melatonin samples over 24 hours). At the end of this visit, participants will receive an orientation to the SHIFT mobile application, where they will be able to assess their prescribed light exposure schedule.

Conditions

Interventions

TypeNameDescription
BEHAVIORALPhototherapyLight exposure recommendations provided by SHIFT mobile application

Timeline

Start date
2022-04-18
Primary completion
2025-03-31
Completion
2025-03-31
First posted
2022-01-11
Last updated
2025-06-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05186233. Inclusion in this directory is not an endorsement.