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Набор скоро начнётся NCT07203170

Evaluation of the Readiness Supportive Leadership Training - National Guard

Без фазы С лечением Psychological Distress Anger Problems Loneliness

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: Readiness Supportive Leadership Training for the National Guard (RESULT-NG).
Кому может быть актуально
Состояния в реестре: Psychological Distress, Anger Problems, Loneliness. Базовые параметры: 18 лет — 89 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
Список центров уточняется — проверьте первичный протокол.
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Evaluating the Effectiveness of Leadership Training for Preventing Risk Factors and Promoting Protective Factors Contributing to Psychological Health

Обзор

The goal of this randomized clinical trial is to evaluate an intervention aimed at increasing the support leaders in the National Guard provide to their subordinates to promote mental health and well-being and reduce risk factors. Survey data will be collected from leaders, service members (SMs) and spouse/partners to evaluate the training effectiveness. The primary objective of the trial is to demonstrate efficacy in the NG, including effects on leaders, SMs, and spouse/partners on the following outcomes: H1: Leaders in the intervention group will demonstrate significant improvements in digital learning effects from pre-test to post-test. H2: The intervention will significantly decrease SM and Leader reports of problematic anger, loneliness, and psychological distress 6-months and then 12-months post-baseline. H3: Spouses/partners of SMs in the intervention group will report decreases in problematic anger, loneliness, and psychological distress at 6 and 12 months. Researchers will compare those in the training intervention group to a wait-list control group. The leadership training builds on a training evaluated in a previous RCT (NCT04152824) adapting from active duty Army to National Guard, including Air NG, and adding an additional facilitated session component. The intervention will include: (1) a 1-hour digital learning utilizing an interactive and self-paced computer-based training, (2) an behavior tracking exercise, and (3) a 1-hour facilitated session, approximately one month later.

Вмешательства

  • Поведенческое Readiness Supportive Leadership Training for the National Guard (RESULT-NG)
    RESULT-NG is a multi-level intervention where leaders receive the training intervention, with evaluation of effects at the subordinate, leader and spouse levels. RESULT-NG consists of three distinct but related components: 1) a 60-minute, multimedia, interactive digital-learning training session, 2) a two-week behavior tracking exercise that takes less than 2 minutes/day after the digital learning to put what was learned into practice, and 3) a 60-minute facilitated session, either in person or

Первичные конечные точки

  • Dimensions of Anger (DAR-5) [Срок оценки: 0 months, 6 months, and 12 months]
  • Depression Subscale- Primary Health Questionnaire (PHQ-9) [Срок оценки: 0 months, 6 months, and 12 months]
  • Brief Loneliness Scale [Срок оценки: 0 months, 6 months, and 12 months.]

Критерии участия

Критерии включения

  • 18 years of age (adults)
  • Employed as a member of the Oregon National Guard (ORNG), including Title 5 and 32 civilians, or is a spouse/partner of an ORNG service member married or cohabitating with the SM for 6 months or more

Критерии исключения

  • Under 18 years of age
  • Not employed as a member of the Oregon National Guard (ORNG), including Title 5 and 32 civilians, or is a spouse/partner of an ORNG service member married or cohabitating with the SM for less than 6 months

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

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Профилактика

Центры проведения

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT07203170 · HT9425-25-1-0668

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗