Actively Recruiting
The Effectiveness of Individualized Imagery Scripts on Sleep, Psychosis, and Suicidality Among Inpatients With Psychosis
Led by The University of Texas Health Science Center, Houston · Updated on 2025-07-16
40
Participants Needed
1
Research Sites
116 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to see how feasible is the use of compact EEG and paired audio technology to administer sleep interventions for inpatients with psychosis, to see if individuals that receive individualized technology-based sleep interventions experience improvements in sleep quality and to see if individuals that receive individualized technology-based sleep interventions experience improvements in symptomatology
CONDITIONS
Official Title
The Effectiveness of Individualized Imagery Scripts on Sleep, Psychosis, and Suicidality Among Inpatients With Psychosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Primary diagnosis of schizophrenia spectrum disorder or mood disorder with psychotic features as determined by treatment team or record review
- Capacity to consent to the study as determined by licensed psychologists or primary attending psychiatrist
- Reported sleep dysfunction indicated by a score of 8 or higher on the Insomnia Severity Index or experiencing nightmares at least once a week
You will not qualify if you...
- Primary substance- or medical-induced psychosis
- Intellectual and developmental disabilities
- Neurodegenerative cognitive disorders
- Presence of implanted devices such as pacemakers
- On one-to-one supervision or 15-minute safety checks for suicidality or aggression
- Patients with roommates who are on 15-minute safety checks to reduce disturbance
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The University of Texas Health Science Center at Houston
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
A
Alia Warner, Ph.D., ABPP
CONTACT
C
Calvary Fielden, B.S.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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