RECRUITING

Shift Worker Intervention for Sleep Health

Conditions

Shift Work Type Circadian Rhythm Sleep Disorder Insomnia, Psychophysiological insomnia shift work nurse sleep psychology behavioral sleep medicine circadian rhythm

Quick Navigation

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

Official Title

Developing a Sleep Health Intervention for Shift Workers

Quick Facts

Study Start:2025-04-28

Study Completion:2028-01-15

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06384742

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 to 65 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion 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)"

Inclusion Criteria

Exclusion 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)"

Contacts and Locations

Study Contact

Jessica R Dietch, PhD

CONTACT

5417371358

jessee.dietch@oregonstate.edu

Liudmyla Kozii, MD, MPH

CONTACT

koziil@oregonstate.edu

Principal Investigator

Jessica Dietch, PhD

PRINCIPAL_INVESTIGATOR

Oregon State University

Study Locations (Sites)

Oregon State University

Corvallis, Oregon, 97331-1102

United States

Collaborators and Investigators

Sponsor: Oregon State University

Jessica Dietch, PhD, PRINCIPAL_INVESTIGATOR, Oregon State University

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 Date2025-04-28

Study Completion Date2028-01-15

Study Record Updates

Study Start Date2025-04-28

Study Completion Date2028-01-15

Terms related to this study

Keywords Provided by Researchers

insomnia
shift work
nurse
sleep psychology
behavioral sleep medicine
circadian rhythm

Additional Relevant MeSH Terms

Shift Work Type Circadian Rhythm Sleep Disorder
Insomnia, Psychophysiological