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Improving Sleep in a Psychiatric Hospital

NCT07010718 · Status: NOT_YET_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2025-06-08

No results posted yet for this study

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.

Conditions

  • Sleep Disorder
  • Mental Health Issue

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

Sponsors & Collaborators

  • The University of Texas Health Science Center, Houston

    lead OTHER

Principal Investigators

  • Michelle Patriquin, PhD, ABPP · The University of Texas Health Science Center, Houston

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-06-01
Primary Completion
2027-06-01
Completion
2028-06-01
FDA Drug
Yes
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07010718 on ClinicalTrials.gov