Optimizing Sleep Health in Nurses

NCT ID: NCT05965609

Last Updated: 2025-03-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-12-08

Study Completion Date

2026-06-30

Brief Summary

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The aim of the proposed study is to pilot test two behavioral sleep intervention strategies for improving insomnia among night shift working nurses.

Detailed Description

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Night shift nurses with insomnia who meet all study criteria will receive one of two insomnia therapies. The specific therapy for insomnia will be determine by chance (like a flip of a coin), with an equal chance to receive either cognitive-behavioral therapy for insomnia or multicomponent relaxation therapy for insomnia, both modified for shift workers. Both therapies will be conducted over telehealth by interventionists trained in behavioral sleep medicine.

Conditions

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Circadian Rhythm Sleep-Wake Disorders, Shift Work Type Sleep Initiation and Maintenance Disorders

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Investigators Outcome Assessors
Participants are asked to refrain from mentioning any information about the treatment they receive when interacting with the investigator or outcomes assessors. Participants are asked not to share details of their treatment with other individuals at their workplace.

Study Groups

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CBTI

Cognitive Behavioral Therapy for Insomnia

Group Type OTHER

CBTI

Intervention Type BEHAVIORAL

Intervention includes education about sleep and behavioral and cognitive strategies to improve sleep

MRTI

Multicomponent Relaxation Therapy for Insomnia

Group Type OTHER

MRTI

Intervention Type BEHAVIORAL

Intervention includes education about sleep and behavioral and relaxation strategies to improve sleep

Interventions

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CBTI

Intervention includes education about sleep and behavioral and cognitive strategies to improve sleep

Intervention Type BEHAVIORAL

MRTI

Intervention includes education about sleep and behavioral and relaxation strategies to improve sleep

Intervention Type BEHAVIORAL

Other Intervention Names

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Cognitive Behavioral Therapy for Insomnia Multicomponent Relaxation Therapy for Insomnia

Eligibility Criteria

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Inclusion Criteria

* Current shift working nursing staff in Oregon
* Expect to continue on shift work schedule during the study
* Meets criteria for an insomnia disorder
* Elevated insomnia symptoms
* Have daily access to internet on a smartphone, tablet, or computer; and
* Can read and write in English

Exclusion Criteria

* People with uncontrolled medical conditions
* Presence of safety risk or condition in which study participation may be ineffective or result in increased risk to safety
* Some current treatments for insomnia
* Permanent day, evening, or rotating shift schedule
* History of seizures or manic episode; or
* Current/expected pregnancy during the study period
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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American Academy of Sleep Medicine

OTHER

Sponsor Role collaborator

Monash University

OTHER

Sponsor Role collaborator

Stanford University

OTHER

Sponsor Role collaborator

Oregon State University

OTHER

Sponsor Role lead

Responsible Party

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Jessee Dietch

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jessica Dietch, PhD

Role: PRINCIPAL_INVESTIGATOR

Oregon State University

Locations

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Oregon State University

Corvallis, Oregon, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Jessica R Dietch, PhD

Role: CONTACT

541-737-1358

Lucy Kozii, MD, MPH

Role: CONTACT

Facility Contacts

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Jessee Dietch, PhD

Role: primary

541-737-1358

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Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

IRB-2021-1200

Identifier Type: -

Identifier Source: org_study_id

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