Condition: Nightmare · Sponsor: Uniformed Services University of the Health Sciences
The overall goal of this Phase IIa randomized controlled pilot trial is to assess the potential efficacy of two emerging treatments for post-trauma nightmares and to test the feasibility of study design and methods. Symptom change will be assessed in two treatment arms: (1) Nightmare Deconstruction and Reprocessing (NDR), an exposure-based psychotherapy; and (2) NightWare (NW), a non-exposure approach using a wristband device. The investigators will also assess the feasibility of circadian-dependent blood sampling and use of another wristband to collect physiologic data. Specific aims are: (1) Compare evidence of how well participants tolerate and comply with the two treatments and test feasibility of methods and procedures; (2) Collect additional evidence of the potential efficacy of two contrasting non-pharmacologic approaches to treating posttraumatic nightmares; (3) Explore the operational stress index (OSI) as a reliable, objective measure of sleep disturbance and nightmare events.
This description comes directly from the study's public registry record.
Patricia Spangler, PhD · 240-620-4076 · patricia.spangler.ctr@usuhs.edu
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| Uniformed Services University of the Health Sciences | Bethesda, Maryland, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06399874