Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06384742

Shift Worker Intervention for Sleep Health

Led by Oregon State University · Updated on 2025-05-02

60

Participants Needed

1

Research Sites

141 weeks

Total Duration

On this page

Sponsors

O

Oregon State University

Lead Sponsor

N

National Heart, Lung, and Blood Institute (NHLBI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim of this study is to pilot test a comprehensive, personalized, media-augmented telehealth intervention ("SWISH") designed to improve sleep health among shift workers.

CONDITIONS

Official Title

Shift Worker Intervention for Sleep Health

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Provision of signed and dated informed consent form
  • Any gender; Ages 18-65
  • Currently employed as a nurse or nursing staff member (e.g., CNA) in the United States
  • Currently have shift work schedules (i.e., stable night shift or rotating shifts that include nights, 62 nights/week) and have worked shift work 62 nights/week for at least 3 months
  • Expect to have a shift work schedule 62 nights/week over the next 6 months
  • Endorse poor sleep, as evidenced by T-score 60 on the PROMIS Sleep Disturbance OR Sleep-Related Impairment measure
  • Have daily access to the internet on a smartphone, tablet, or computer
  • Can read and write in English.
Not Eligible

You will not qualify if you...

  • Conditions which make study treatment likely to be ineffective such as current chronic use of medications that interfere with sleep, alcohol or substance use disorder, thought disorder (per DIAMOND psychiatric interview), unstable sleep or medical conditions needing care beyond study treatments (e.g., untreated sleep apnea)
  • Presence of safety risk or condition increasing risk from participation (e.g., high suicide risk, uncontrolled seizure disorder, history of manic or hypomanic episode, current pregnancy)
  • Currently receiving non-pharmacological treatment for insomnia or unstable hypnotic/alerting medication use
  • Currently participating in other research studies with significant overlap in methods or procedures

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Oregon State University

Corvallis, Oregon, United States, 97331-1102

Actively Recruiting

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Research Team

J

Jessica R Dietch, PhD

CONTACT

L

Liudmyla Kozii, MD, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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