NCT06105307
Using Cognitive-Behavioral Change and Mobile Technology to Improve RN Sleep and Fatigue
Enrolling by Invitation
NAAges 18+InterventionalPreventionUniversity of CincinnatiInvestigator-initiated
~76 participants
Updated 2026-04-30 on ClinicalTrials.gov
What's tested:RN-SLEEPHealthy Habit - Educational Control
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Sleep Duration
Measured over Baseline and post-intervention (4 and 8-weeks)
+1 more outcome measured
Conditions
Where it's being run
1 sites across 1 statesOhio1
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
working night shift for a minimum of 6-months
have access to a smart phone.
Exclusion
who are pregnant or the parent of child(ren) less than 1 year of age
who have a diagnosed sleep disorder.
What this trial measures
- Sleep DurationBaseline and post-intervention (4 and 8-weeks)
Sleep duration will be measured using a 7-day data collection of movement via actigraphy. Daily sleep diaries will support the actigraphy data.
- Sleep QualityBaseline and post-intervention (4 and 8-weeks)
Sleep quality will be measured via self-report survey, the PROMIS Sleep Related Disturbance.