The Effectiveness of Individualized Imagery Scripts on Sleep, Psychosis, and Suicidality Among Inpatients With Psychosis
Status
Conditions
Treatments
Details and patient eligibility
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
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- primary diagnoses of schizophrenia spectrum disorder or mood disorder with psychotic features, as determined by the treatment team or record review
- capacity to consent to the study as determined by licensed psychologists ( or the primary attending psychiatrist
- reported sleep dysfunction which will be determined by a subthreshold or more severe score ≥ 8 on the Insomnia Severity Index (ISI), and/or report experiencing nightmares at least once a week.
Exclusion criteria
- primary substance- or medical-induced psychosis
- intellectual and developmental disabilities
- neurodegenerative cognitive disorders
- implanted devices (e.g., Pacemakers)
- on one-to-one supervision or 15-minute safety checks for suicidality or aggression
- patients with roommates that are on 15-minute checks to minimize impact on study participants' awakenings
Trial design
Primary purpose
Allocation
Interventional model
Masking
40 participants in 2 patient groups
Trial contacts and locations
Loading...
Central trial contact
Alia Warner, Ph.D., ABPP; Calvary Fielden, B.S.
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal