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Clinical Trial Summary

The primary aim of this study is to investigate the feasibility, acceptability, and preliminary efficacy of an adapted Cognitive Behavioral Therapy - Insomnia (CBT-I) intervention in improving sleep in a firefighter population.


Clinical Trial Description

After being informed about the study and potential risks, participants will be randomized to the intervention group (group to receive CBT-I) or the no-intervention control group. All participants in the study will complete three assessment visits; one prior to the start of the intervention, one immediately following the 6-week intervention, and one 3-months post-intervention. The intervention group will engage in 6-weeks of CBT-I training aimed at targeting sleep and sleep-related concerns faced as a result of occupational considerations. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05087121
Study type Interventional
Source Pacific University
Contact
Status Completed
Phase N/A
Start date February 16, 2021
Completion date July 31, 2022

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