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NOT YET RECRUITING
NCT07010718
PHASE1

Improving Sleep in a Psychiatric Hospital

Sponsor: The University of Texas Health Science Center, Houston

View on ClinicalTrials.gov

Summary

The purpose of this study is to examine effects of sleep promotion versus treatment as usual (TAU) on subjective, self-reported sleep while in inpatient psychiatric treatment, to examine effects of sleep promotion vs. TAU/sleep disruption on self-reported depression, anxiety, suicide risk across inpatient length of stay, readmission at 72 hours, objective sleep and to compare implementation outcomes of acceptability and feasibility of sleep promotion relative to TAU/sleep disruption as reported by patients, clinicians, and clinic leaders using mixed methods.

Official title: Comparative Effectiveness Trial of Sleep Promotion vs. Disruption in High Suicide Risk Inpatients

Key Details

Gender

All

Age Range

18 Years - 90 Years

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2025-06-01

Completion Date

2028-06-01

Last Updated

2025-06-08

Healthy Volunteers

No

Interventions

DRUG

Scented Oil

inpatient-safe aromatherapy (scented oil)

DEVICE

Ear Plugs

ingestible-safe ear plugs (noise blocking)

DEVICE

Eye Mask

inpatient-safe eye mask (light blocking).

BEHAVIORAL

Video based safety check

video based safety checks will be conducted as long as participants are in bed and asleep

BEHAVIORAL

In person safety check

In person safety checks will be conducted every 30 minutes

Locations (1)

The University of Texas Health Science Center at Houston

Houston, Texas, United States