RECRUITING

A Pilot of a Personalized Circadian MHealth to Improve Sleep in Night Shift Workers

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 goal of this project is to establish the evidence base for equitable accessibility and implementation of the precision sleep medicine mobile application, SHIFT.

Official Title

A Pilot of a Personalized Circadian MHealth to Improve Sleep in Night Shift Workers

Quick Facts

Study Start:2023-10-23
Study Completion:2027-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06809335

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 CriteriaExclusion Criteria
  1. * Inadequate sleep duration (habitual sleep less than 7 hours during the day)
  2. * Willingness to download the SHIFT app and follow the lighting recommendations
  3. * Ability to follow a set sleep schedule of 7 hours in bed after the night shifts
  4. * Working at least 4 night shifts a month
  5. * Shifts that must begin between 18:00 and 02:00 and last 8 to 12 hours
  6. * Score of 8 or above on the Epworth Sleepiness scale and/or a score of 8 or above on the Insomnia Severity Index
  1. * Other independent sleep disorders (e.g., obstructive sleep apnea, narcolepsy, etc.)
  2. * History of seizures or other significant neurological disorders
  3. * Bipolar disorder
  4. * Termination of shift schedule
  5. * Pregnancy
  6. * Current use of medications that impact sleep-wake functioning
  7. * Alcohol and substance use disorder

Contacts and Locations

Study Contact

Philip Cheng, PhD
CONTACT
248-344-7361
pcheng1@hfhs.org
Marleigh Treger, BS
CONTACT
248-344-8028
mtreger1@hfhs.org

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 Date2023-10-23
Study Completion Date2027-06

Study Record Updates

Study Start Date2023-10-23
Study Completion Date2027-06

Terms related to this study

Additional Relevant MeSH Terms

  • Shift Work Sleep Disorder