Purpose

Sleep is often a challenge for nightshift workers because their work and sleep schedules are inverted. Sleep is commonly measured using actigraphy, which is the standard measure of objective sleep in the general population; however, this method has substantial limitations for nightshift workers because the standard legacy algorithms only correctly identify 50.3% of daytime sleep. This significantly reduces the validity for nightshift workers. The purpose of this study is to test a novel method to expand actigraphy by using 1) a multi-sensor approach that 2) uses machine learning (ML) algorithms to increase the accuracy of detecting daytime sleep.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Participants must be working a fixed nightshift schedule, operationalized as: a) working at least three night shifts a week, b) shifts must begin between 18:00 and 02:00, and last between 8 to 12 hours, and c) must also plan to maintain the nightshift schedule for the duration of the study - Participants must have worked the nightshift for at least six months - Must plan to maintain the nightshift schedule for the duration of the study - Participants must be at least 18 years old

Exclusion Criteria

  • Termination of nightshift schedule or planned travel during the study period - Does not have at least an average of 8-hour time bed opportunity per 24-hour period - Unwilling to integrate the study smart sensors in their bedroom environment - Illicit drug use via self-report and urine drug screen - History of neurological disorders - Alcohol use disorder - Pregnancy

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Non-Randomized
Intervention Model
Sequential Assignment
Intervention Model Description
Type I hybrid effectiveness-implementation trial with two steps. Step 1: In-lab trial (with a sample of participants balanced on degree of technological literacy) comparing data processing using legacy actigraphy to multi-sensor machine learning. Step 2: At-home implementation of multi-sensor machine learning approach (balanced by technological literacy).
Primary Purpose
Other
Masking
Double (Participant, Investigator)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Single vs Multi-Sensor Sleep Tracking In-Lab
In Part 1 of the study, all participants' data will undergo two separate methods for analyzing sleep. The legacy actigraphy algorithm methods will use only raw accelerometer data from a single sensor collected and processed using legacy actigraphy algorithms. The legacy algorithm is comprised first of reducing accelerometer data into activity counts per epoch, which will then be categorized into sleep or wake in accordance with the Cole-Kripke algorithm. The multi-sensor machine learning (ML) method will use raw accelerometer data in addition to data from additional sensors from the watch, phone, and other smart sensors in the sleeping environment. These data will be processed using a machine learning algorithm.
  • Other: Single-Sensor Tracking (In-Lab)
    In-lab sleep tracking using only raw accelerometer data from a single sensor collected and processed with legacy actigraphy algorithms.
  • Other: Multi-Sensor Sleep Tracking (In-Lab)
    In-lab sleep tracking using raw accelerometer data and additional sensors collected and processed with machine learning.
    Other names:
    • Multi-sensor ML
    • Multi-Sensor Machine Learning
Other
Multi-Sensor Sleep Tracking At-Home
This condition includes 4 weeks of at-home sleep tracking using the multi-sensor approach. Daily sleep diaries will also be collected to enable data quality check. Once collected, all data will be processed with the same machine learning algorithm used in the in-lab experimental condition.
  • Other: Multi-Sensor Sleep Tracking (At-Home)
    At-home sleep tracking using raw accelerometer data and additional sensors collected and processed with machine learning.

Recruiting Locations

Henry Ford Columbus Medical Center
Novi 5004062, Michigan 5001836 48377
Contact:
Philip Cheng, PhD
248-344-7361
pcheng1@hfhs.org

More Details

Status
Recruiting
Sponsor
Henry Ford Health System

Study Contact

Philip Cheng, PhD
248-344-7361
pcheng1@hfhs.org

Detailed Description

The first aim of this study is to establish an open-source machine learning algorithm for sleep tracking that outperforms legacy actigraphy algorithms in detecting daytime sleep periods. The second aim is to enhance tracking of sleep continuity variables by adding multiple sensors. The final aim is to identify facilitators and barriers of at-home implementation of multi-sensor sleep tracking. Our central hypothesis is that a multi-sensor ML approach will outperform legacy algorithms against gold-standard polysomnography (PSG). This study will be type I hybrid effectiveness-implementation trial that 1) validates the proposed multi-sensor ML approach using in-lab polysomnography, and 2) examines implementation of the multi-sensor ML approach in an ecologically valid setting via an at-home implementation for four weeks. A sample of nightshift workers will be enrolled in the in-lab validation portion of the study and will be hooked-up to PSG with continuous data collection for the duration of the lab visit to capture five planned sleep opportunities at varying lengths (4 hr, 2 hr, 1.5 hr, and two 30-minute naps; 8 hrs total). For each participant, sensor data will be processed using two separate methods. For the legacy actigraphy algorithm method, only raw accelerometer data will be processed. For the multi-sensor machine learning method, accelerometer data from the watch along with additional sensors will be processed using a machine learning algorithm. Some participants who complete the in-lab portion of the study will be asked to complete the at-home portion of the study, which includes 4 weeks of at-home sleep tracking using the multi-sensor approach. Participants will receive the sensor kit and will have an at-home appointment with study staff to aid with sensor set-up, which will then be collected again at the end of the 4-week period. Daily sleep diaries will also be collected during the 4 weeks to enable data quality check.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.