RECRUITING

Shift Worker Intervention for Sleep Health

Description

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.

Study Overview

Study Details

Study overview

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.

Developing a Sleep Health Intervention for Shift Workers

Shift Worker Intervention for Sleep Health

Condition
Shift Work Type Circadian Rhythm Sleep Disorder
Intervention / Treatment

-

Contacts and Locations

Corvallis

Oregon State University, Corvallis, Oregon, United States, 97331-1102

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * 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, \>=2 nights/week) and have worked shift work \>=2 nights/week for at least 3 months
  • * Expect to have a shift work schedule \>=2 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, table, or computer; and
  • * Can read and write in English.
  • * Conditions which make study treatment likely to be ineffective. For example, current chronic use of medications that interfere with sleep, alcohol or substance use disorder, or thought disorder (as determined by DIAMOND psychiatric interview), unstable sleep or medical conditions that necessitate additional medical care not provided by study treatments (e.g., known untreated sleep apnea).
  • * Presence of safety risk or condition in which study participation may result in increased risk to safety (e.g., elevated risk for suicide, self-reported uncontrolled seizure disorder, history of manic or hypomanic episode, current pregnancy),
  • * Currently receiving non-pharmacological treatment for insomnia (e.g., cognitive behavioral therapy for insomnia) and/or current unstable hypnotic/alerting medication use OR
  • * Currently participating in other research studies with substantial overlap in terms of methods/procedures (e.g., PI's ongoing study "Piloting an Adaptation of Cognitive Behavioral Therapy for Insomnia for Shift Workers (CBTI-Shift)"

Ages Eligible for Study

18 Years to 65 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Oregon State University,

Jessica Dietch, PhD, PRINCIPAL_INVESTIGATOR, Oregon State University

Study Record Dates

2028-01-15