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Клиническое исследование

Nightmare Deconstruction and Reprocessing vs. NightWare Wristband

NCT: NCT06399874 · ACTIVE_NOT_RECRUITING

NCT IDNCT06399874
СтатусACTIVE_NOT_RECRUITING
Дата начала2024-06-11
SponsorUniformed Services University of the Health Sciences (FED)
First posted
Last updated

Краткое описание

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.

Официальный источник

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Данные получены через API ClinicalTrials.gov. Актуальный статус смотрите в официальной записи.

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