Меню
Идёт набор NCT05631743

VR-CBT With Inuit in Quebec

Без фазы С лечением Emotion Regulation

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: VR-CBT, Self-management.
Кому может быть актуально
Состояния в реестре: Emotion Regulation. Базовые параметры: 14 лет — 60 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
Канада
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

A Virtual Reality-assisted Cognitive Behavior Therapy With Inuit in Quebec - a Proof-of-concept Randomized Controlled Trial

Обзор

The study design is a two-arm randomized controlled pilot trial. The investigators will recruit Inuit in Montreal and randomly assign them to two treatment groups (n=20 each). The active psychotherapy group will receive a ten-week manualized virtual reality (VR) assisted cognitive-behavioral psychotherapy (VR-CBT) at the clinic and guided by a psychotherapist. The VR-CBT will aim at improving emotion regulation. The comparison group will use a VR self-management program, Calm Place, for guided relaxation during ten weeks at home. To evaluate outcome in both groups, the researchers will measure self-reports of emotion regulation, affect, distress and well-being, as well as a psychophysiological reactivity paradigm pre-post treatment.

Подробное описание

In this protocol, the investigators present a proof-of-concept trial that will evaluate an active psychotherapy and self-management, both targeting emotion regulation skills. The study design is a two-arm randomized controlled trial. The investigators will recruit Inuit and randomly assign them to two treatment groups (n=20 each). The active psychotherapy group will receive a ten-week manualized virtual reality (VR) assisted cognitive-behavioral psychotherapy (VR-CBT) at the clinic and guided by a psychotherapist. The VR-CBT will aim at improving emotion regulation, a set of skills or competence that is impacted by traumatic experiences and mediates the effect of trauma on psychiatric symptoms. The investigators conducted a cultural adaptation of the therapy for Inuit with a co-design grounded in qualitative participatory methods. The comparison group will use a VR self-management program, Calm Place, for guided relaxation during ten weeks at home. To evaluate outcome in both groups, the researchers will include a psychophysiological reactivity paradigm pre-post treatment and self-reports of emotion regulation, anxiety, mood, substance use, functionality and quality of life. The investigators expect to see preliminary evidence that our VR-CBT can be more successful than guided VR relaxation with Calm Place (self-management) decreasing difficulties in emotion regulation, psychiatry symptoms, increasing well-being, and normalizing responses to stressful stimuli (reactivity).

Вмешательства

  • Поведенческое VR-CBT
    The therapy is focused on emotion regulation through guided learning in virtual reality. The manual is a modified conventional cognitive behavioral therapy to include these aspects and the suggestions of an advisory committee of Inuit and non-Inuit health service providers (e.g., cultural adaptation).
  • Поведенческое Self-management
    The previously developed commercial VR program involves guided relaxation and meditation techniques.

Первичные конечные точки

  • Emotion Regulation [Срок оценки: Approximately 5 minutes]
Вторичные конечные точки (12)
  • heart rate [Срок оценки: Approximately 1 hour testing session.]
  • heart rate variability [Срок оценки: Approximately 1 hour testing session.]
  • skin conductance response [Срок оценки: Approximately 1 hour testing session.]
  • anxiety (momentary) [Срок оценки: Approximately 1 hour testing session.]
  • emotional arousal (momentary) [Срок оценки: Approximately 1 hour testing session.]
  • emotional valence (momentary) [Срок оценки: Approximately 1 hour testing session.]
  • Psychiatric Symptoms (anxiety) [Срок оценки: Administration time is around 3 minutes]
  • Psychiatric Symptoms (depression) [Срок оценки: Administration time is around 4 minutes]
  • Psychiatric Symptoms (post traumatic stress disorder) [Срок оценки: Administration time is between 2 minutes]
  • Psychiatric Symptoms (alcohol use disorder) [Срок оценки: Administration time is between 2 minutes]
  • Psychiatric Symptoms (substance use disorders) [Срок оценки: Administration time is between 4 minutes]
  • Psychological distress and well being: Clinical outcome in routine evaluation outcome measure and 10 item (CORE- OM/10) [Срок оценки: Approximately 10 minutes]

Критерии участия

Критерии включения

  • Self-identify as Inuk
  • Live in Montreal
  • be between 14 to 60 years of age
  • be proficient in English or French
  • No history of cardiac conditions
  • No history of epilepsy
  • Can provide an emergency contact
  • Tolerance of VR headset
  • Tolerance of sensors
  • Has no current suicidal or homicidal risk
  • No history of psychosis or schizophrenia
  • Current stable mood
  • Is generally mentally stable
  • Score less than 8 on the Alcohol Use Disorders Identification Test C
  • Score less than 3 on the Drug Abuse Screen Test (10 item version)
  • Not have had any change in psychoactive medications during 4 weeks preceding screening and inclusion to the study

Критерии исключения

  • does not identify as Inuk
  • youth below the age of 14 and adults above the age of 60.
  • self-reported history of psychosis or schizophrenia
  • current substance abuse, as measured by two screens (AUDIT-C, DAST-10)
  • other mental or physical condition that might preclude them from the trial (i.e., pre-existing heart conditions, convulsions, acute mental health risk).

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
Открытое
Основная цель
Лечение

Центры проведения

Канада · 1 центр
  • Douglas Mental Health University Institute — Montreal

Идентификаторы

NCT: NCT05631743 · IUSMD 21-52

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗