Early Intervention to Prevent Development of PTSD in Burn Survivors and Their Caregivers
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: Promotion of Emotional Disclosure for Burns (PoED-B), minimally Enhanced Usual Care control (mEUC).
- Кому может быть актуально
- Состояния в реестре: Posttraumatic Stress Disorder, Burns, Traumatic Injury, Acute Stress Disorder. 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 →
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Обзор
The purpose of this clinical trial is to adapt and test a brief patient-caregiver early intervention designed to reduce posttraumatic stress symptoms in hospitalized burn patients and their caregivers. This intervention is a brief, 4-session cognitive-behavioral intervention designed for burn patients and their loved one to complete together, during and after hospitalization. The intervention targets relational communication and functioning through reduction of invalidating, negative statements and avoidant coping by teaching patients and their loved ones to engage in adaptive natural disclosures, supportive responses, and approach coping after the burn trauma. The intervention uses evidence-based psychotherapy techniques, including psychoeducation, motivational interviewing, and skills coaching. The clinical trial will occur in two sequential phases. In the first phase of the study (case series), the intervention will be provided to two burn patient-caregiver dyads (four adults) to pilot test the intervention, seek patient and provider feedback, and refine the intervention. All four adults will receive the intervention. In the second phase of the study, the randomized controlled trial (RCT) phase, investigators will enroll 20 more burn patient-caregiver dyads (40 more adults) who will be randomly assigned (like the flip of a coin) at the dyad level to receive the intervention or a burn survivor-only minimally enhanced usual care psychoeducation control condition (mEUC). The goals of the RCT phase are to study whether the intervention is acceptable to patients, feasible to conduct, and whether the intervention improves burn survivor-caregiver healthy relationship communication about difficult events and treatment outcomes compared to mEUC.
Вмешательства
- Поведенческое Promotion of Emotional Disclosure for Burns (PoED-B)
PoED-B is a dyadic treatment where both patient and identified informal caregiver participate. PoED-B targets reducing disclosure-constraining behaviors (e.g., invalidating, negative statements) using psychoeducation, motivational interviewing, and skills training. The goal is to encourage the patient-caregiver dyad to engage in natural disclosures, supportive responses, and approach coping after the burn trauma to facilitate emotional processing. It is four sessions long. Delivery format takes - Поведенческое minimally Enhanced Usual Care control (mEUC)
mEUC is an individually-administered psychoeducation control for burn patients modeled after minimally enhanced care in acute care surgery units. In one 30-minute session, the therapist reviews with the participant a standardized psychoeducation handout on common psychological reactions after burn injury, giving them time to ask questions or express concerns within a supportive therapy framework. Then, the participant is given the handout, which also includes self-help skills. After study comple
Первичные конечные точки
- Social Constraints Scale [Срок оценки: Before treatment, immediately after ending treatment, 6-week follow-up]
- Feasibility of Recruitment [Срок оценки: baseline]
- Feasibility of Data Collection [Срок оценки: From enrollment to the end of study assessments at 6-weeks posttreament]
- Acceptability: Satisfaction with Treatment [Срок оценки: Immediately after ending treatment]
- Acceptabilitly: Retention [Срок оценки: Immediately after ending treatment]
- Acceptability: Global Improvement Rating [Срок оценки: Immediately after ending treatment]
Вторичные конечные точки (6)
- PTSD Checklist for DSM-5 (PCL-5) [Срок оценки: Pretreatment, Immediately after ending treatment, 6-week follow-up]
- Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) [Срок оценки: Immediately after ending treatment, 6-week follow-up]
- Hospital Anxiety and Depression Scale (HADS) [Срок оценки: Pretreatment, immediately after ending treatment, 6-week follow-up]
- MINI Montreal International Neuropsychiatric Interview v. 7.0.2 (MINI) [Срок оценки: Pretreatment, immediately after ending treatment, 6-week follow-up]
- Dyadic Relationship Scale (DRS) [Срок оценки: Pretreatment, immediately after ending treatment, 6-week follow-up]
- Significant Other's Responses to Trauma Scale (SORTS) [Срок оценки: Pretreatment, immediately after ending treatment, 6-week follow-up]
Критерии участия
Критерии включения
- Alert, oriented, \& not withdrawing from substance at time of screening
- Can read and write in English
- Hospitalized within 10 days of burn injury
- Anticipated discharge <=4 weeks
- Have an email, mailing address, and at least 1 smart device for telehealth sessions
- PTSD risk score of 2 or greater (patient-only)
- Willing to attend therapy sessions with a loved one
Критерии исключения
- Currently incarcerated or in police custody
- > 10 days post-burn
- Lifetime diagnosis of primary psychosis or intellectual disability
- Ongoing reported domestic violence in the dyad
- Unstable bipolar disorder, severe substance use disorder, or acute suicidality with imminent intent that does not remit within 10 days of burn-injury
- Inflammation Confounds (patient-only) of BMI > 40, metabolic syndrome, admission A1C of >= 6.5%
- Currently receiving couples therapy
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
- Простое слепое
- Основная цель
- Профилактика
Центры проведения
США · 1 центр
- University of Southern California, Keck School of Medicine & Los Angeles General Medical C — Los Angeles
Идентификаторы
NCT: NCT07656545 · HS-25-00383 · 1K23MH141296-01