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Use of Consumer Sleep Technology to Treat Shift Work Disorder

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2022-04-18

Study Completion:2025-03-31

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:COMPLETED

Study ID

NCT05186233

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Participants must work at least 2 night shifts a week * Participants must have night shifts starting between 18:00 and 02:00 and lasting 8 to 12 hours * Participants must have maintained this night shift schedule for at least 6 months * Participants must have Shift Work Disorder, diagnosed based on ICSD-3 criteria	* Medical history of central nervous system disorders * Medical history of other sleep disorders * Diagnosis of an unstable major medical condition medical chart review * Dependence on alcohol (≥ 4 beverages a day) * Heavy tobacco use (≥ 10 cigarettes per day) * Recreational drug use * Use of medications impacting central nervous system functioning * Caffeine use in excess of 5-6 servings (\~ 600mg) per day * Pregnancy

Inclusion Criteria

Exclusion Criteria

* Participants must work at least 2 night shifts a week
* Participants must have night shifts starting between 18:00 and 02:00 and lasting 8 to 12 hours
* Participants must have maintained this night shift schedule for at least 6 months
* Participants must have Shift Work Disorder, diagnosed based on ICSD-3 criteria

* Medical history of central nervous system disorders
* Medical history of other sleep disorders
* Diagnosis of an unstable major medical condition medical chart review
* Dependence on alcohol (≥ 4 beverages a day)
* Heavy tobacco use (≥ 10 cigarettes per day)
* Recreational drug use
* Use of medications impacting central nervous system functioning
* Caffeine use in excess of 5-6 servings (\~ 600mg) per day
* Pregnancy

Contacts and Locations

Study Locations (Sites)

Henry Ford Columbus Medical Center

Novi, Michigan, 48377

United States

Collaborators and Investigators

Sponsor: Henry Ford Health System

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-04-18

Study Completion Date2025-03-31

Study Record Updates

Study Start Date2022-04-18

Study Completion Date2025-03-31

Terms related to this study

Additional Relevant MeSH Terms

Shift-work Disorder