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Идёт набор NCT07069517

Accelerated Treatment for Co-occurring Insomnia, Nightmares, and PTSD

Без фазы С лечением Insomnia PTSD - Post Traumatic Stress Disorder Nightmares

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Cognitive-Behavioral Therapy for Insomnia (CBTi), Cognitive Behavioral Therapy for Nightmares (CBTn), Written Exposure Therapy (WET), Sleep Hygiene.
Кому может быть актуально
Состояния в реестре: Insomnia, PTSD - Post Traumatic Stress Disorder, Nightmares. Базовые параметры: 18 лет — 65 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Accelerated Treatment for Co-occurring Insomnia, Nightmares, and PTSD: A Randomized Controlled Trial

Обзор

This study is a two-arm individually randomized group treatment clinical trial evaluating behavioral therapies for insomnia, nightmares, and PTSD. The study will compare cognitive-behavioral therapy for insomnia and nightmares to sleep hygiene (Control), both integrated with Written Exposure Therapy for PTSD and delivered in an accelerated (i.e., 5-day) group treatment format, preceded and followed by individual treatment sessions. 160 participants will be randomized into one of two study conditions.

Подробное описание

The aims of the study are:

1. Determine the efficacy of accelerated cognitive behavioral therapy for insomnia and nightmares (CBTi+n) integrated with Written Exposure Therapy (WET) for PTSD for improving insomnia symptoms among military personnel with clinically significant symptoms of insomnia, nightmares, and PTSD. 2. Determine the efficacy of accelerated CBTi+n integrated with WET for improving nightmare symptoms among military personnel with clinically significant symptoms of insomnia, nightmares, and PTSD.

Exploratory Aim: Determine the efficacy of accelerated CBTi+n integrated with WET for improving PTSD symptoms among military personnel with clinically significant symptoms of insomnia, nightmares, and PTSD.

Вмешательства

  • Поведенческое Cognitive-Behavioral Therapy for Insomnia (CBTi)
    CBTi focuses on stimulus control, eliminating maladaptive coping habits, reducing arousal, and challenging maladaptive thoughts about sleep in an effort to reduce time to fall asleep and time awake during the night.
  • Поведенческое Cognitive Behavioral Therapy for Nightmares (CBTn)
    CBTn involves writing about a distressing or frequent nightmare, rewriting the narrative of the nightmare to target trauma-related themes, and reading the rescripted nightmare narrative.
  • Поведенческое Written Exposure Therapy (WET)
    WET is a trauma-focused intervention in which individuals write about their worst traumatic experience following scripted instruction from the therapist.
  • Поведенческое Sleep Hygiene
    Involves reviewing sleep diary data, sleep education, and reviewing and discussing sleep hygiene practices.

Первичные конечные точки

  • Posttraumatic Stress Disorder Checklist (PCL-5) [Срок оценки: Change from baseline through 3 and 6 month follow-up assessment]
  • Insomnia Severity Index (ISI) [Срок оценки: Change from baseline through 3 and 6 month follow up]
  • Nightmare Disorders Index [Срок оценки: Change from baseline through 3 and 6 month assessments]
Вторичные конечные точки (7)
  • Clinician Administered PTSD Scale (CAPS-5) [Срок оценки: Change from baseline to 1-month follow-up assessment]
  • Structured Clinical Interview for DSM-5 Sleep Disorders- Revised (SCISD-R) [Срок оценки: Change from baseline to 1-month follow-up assessment]
  • Generalized Anxiety Disorder Screener (GAD-7) [Срок оценки: Change from baseline through 3 and 6 month follow-up assessment]
  • Trauma-Related Nightmare Survey (TRNS) [Срок оценки: Change from baseline through 3 and 6 month follow-up assessment]
  • Depressive Symptoms Index-Suicidality Subscale (DSI-SS) [Срок оценки: Change from baseline through 3 and 6 month follow up assessment]
  • Patient Health Questionnaire-9 (PHQ-9) [Срок оценки: Change from baseline through 3 and 6 follow-up assessment]
  • Brief Inventory of Psychosocial Functioning (B-IPF) [Срок оценки: Change from baseline through 3 and 6 month follow up]

Критерии участия

Критерии включения

  • Defense Enrollment Eligibility Reporting System (DEERS) eligible active-duty military personnel or veteran, 18-65 years old.
  • Ability to speak and read English.
  • Clinically significant PTSD symptoms (CAPS-5 > 25 with at least one Intrusion symptom and at least one Avoidance symptom).
  • Clinically significant symptoms of insomnia disorder (Structured Clinical Interview for Sleep Disturbance DSM-5 (SCISD) Insomnia Criteria are met and Insomnia Severity Index (ISI) > 11).
  • Nightmares > 1 monthly (as reported on the SCISD).
  • Willing to refrain from new behavioral health or medication treatment for issues pertaining to PTSD, sleep, and nightmares during study participation.

Критерии исключения

  • Current suicide or homicide risk meriting crisis intervention.
  • Inability to comprehend the baseline screening questionnaires.
  • Unwilling to remain abstinent from alcohol during therapy sessions.
  • Serious mental health symptoms, such as mania, psychosis, alcohol or substance use disorders warranting immediate clinical attention based on interviewer assessment and clinical judgement.
  • Currently engaged in evidence-based psychotherapy for PTSD (e.g., Prolonged Exposure Therapy, Cognitive Processing Therapy, Written Exposure Therapy) or insomnia or nightmares (e.g., Cognitive Behavioral Therapy for Insomnia or Nightmares).
  • Pregnancy, as determined by self-report, because pregnancy can adversely affect sleep outside of PTSD, insomnia, and nightmares.
  • Working duty shifts ending later than 21:00 or starting before 05:30 more than 2 times per month.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Простое слепое
Основная цель
Лечение

Центры проведения

США · 1 центр
  • Fort Hood — Kileen

Идентификаторы

NCT: NCT07069517 · MCA0010

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗