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Набор скоро начнётся NCT07584252

The Healing and Empowerment Actions for Recovery From Trauma (HEART) Trial

Без фазы С лечением Trauma Blunt Orthopedic

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: Comprehensive trauma recovery programming (C-TRP), Standard of Care (Investigator Selected).
Кому может быть актуально
Состояния в реестре: Trauma Blunt, Orthopedic. Базовые параметры: от 18 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 →

Обзор

The HEART Trial aimed to determine if wrap-around psychosocial support for patients who sustain moderate to severe trauma requiring orthopedic surgery intervention improves outcomes for patients (Aim 1), care-partners (Aim 2), and healthcare workers (Aim 3) as well as explore implementation strategies to improve health systems' capabilities and capacity to integrate psychosocial support services. The comparators represent real healthcare options for patients, caregivers, and healthcare workers. The HEART Trial is a multicenter pragmatic, stepped-wedge cluster randomized, hybrid type I comparative effectiveness-implementation superiority trial. The study intervention (C-TRP) is a trauma-focused psychosocial intervention, with each site serving as its own control (TRP).

Вмешательства

  • Поведенческое Comprehensive trauma recovery programming (C-TRP)
    A multicomponent, patient-focused intervention that follows the standardized recovery protocol (TRP) with added resiliency coaching, peer support, education, and navigation resources. C-TRP begins during hospitalization and continues throughout recovery, allowing patients and care-partners to engage based on their needs and preferences. Upon enrollment, patients are connected with a local resiliency coach from Evellere for optional in-person support. Coaching provides a holistic approach to ensu
  • Другое Standard of Care (Investigator Selected)
    Every trauma system adheres to a standardized protocol, aligned with credentialing requirements of ATS and The Joint Commission. Locally, this involves tailored referrals by hospital teams at time of discharge, based on specific needs of the patient. Additionally, a standard after-visit summary, with discharge instructions, is provided to the patient. It is a routine practice for the discharge team to review these instructions with the patient to address any questions. After discharge, the respo

Первичные конечные точки

  • PROMIS-Anxiety [Срок оценки: 5-7 weeks and 12-14 weeks post enrollment]
Вторичные конечные точки (1)
  • Maslach Burnout Inventory [Срок оценки: 6 months and 12 months]

Критерии участия

Patients:

Критерии включения

  • Age >= 18 years
  • Anticipated hospital length of stay > 72 hours
  • Moderate to severe orthopaedic trauma treated surgically for 1 or more injuries
  • GCS >= 13 at the time of enrollment
  • Willing and able to meet with Evellere coach while hospitalized or via the telephone within 72 hours of discharge (intervention cohort only)

Критерии исключения

  • Non-english speaking (must be sufficiently fluent in English to consent and complete surveys without interpretive services)
  • Prior to index hospitalization, patient must not be receiving home services or be independent in daily tasks
  • Any penetrating brain injury
  • Patients with significant burn injury
  • Prior cognitive impairment
  • Hospital death or imminent death
  • Hospice care at time of trauma or selection for hospice during initial hospital admission or do not resuscitate or comfort care only before index visit
  • Prisoner/ inmate or police/ security intervention during hospitalization
  • No reliable internet access at baseline
  • Psychosis
  • Trauma presentation is a result of suicide attempt/ self-harm

Care Partners

Критерии включения

  • Identified by the enrolled patient as a primary source of support during their recovery. A care partner can be in person or supporting remotely.
  • Age >= 18 years
  • Willing and able to meet with an Evellere coach during patient hospitalization or via telephone within 72 hours of discharge (intervention cohort only)

Критерии исключения

  • Non-english speaking (must be sufficiently fluent in English to consent and complete surveys without interpretive services)
  • Paid professionals or home healthcare providers whose support is provided as part of employment (e.g., nurses, aides, case managers)
  • Already enrolled as a care partner for another participant in the HEART Trial
  • Hospitalized at time of patient enrollment
  • No reliable internet access at baseline

Healthcare Workers

Критерии включения

  • Age > 18 years
  • Currently employed (full-time, part-time) at a participating trauma center in a role type associated with trauma care (e.g., engaged in clinical care navigation, behavioral health, rehabilitation, recovery coordination, etc.)
  • Provides or supports care for orthopedic trauma patients for ≥20% of their clinical time
  • Expected to remain employed at the trauma center for >12 months after enrollment

Критерии исключения

  • Are contracted staff or traveling temporary staff
  • Are students or trainees
  • No reliable internet access at baseline

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Последовательный дизайн
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

США · 7 центров
  • University of Colorado Anschutz — Aurora
  • R Adams Cowley Shock Trauma Center — Baltimore
  • Johns Hopkins University — Baltimore
  • Hennepin Healthcare — Minneapolis
  • Dartmouth Hitchcock Medical Center — Lebanon
  • The Ohio State University — Columbus
  • Vanderbilt University — Nashville

Идентификаторы

NCT: NCT07584252 · BPS-2024C3-41889

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗