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Идёт набор NCT05486793

Treatment for Antepartum Posttraumatic Stress Disorder/PTSD Study

Без фазы С лечением PTSD

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: Written Exposure Therapy (WET), Emotion Focused Supportive Therapy (EFST).
Кому может быть актуально
Состояния в реестре: PTSD. Базовые параметры: 18 лет — 50 лет · Женщины.
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

A Non-Inferiority Trial Testing Delivery of Written Exposure Therapy by Community Health Workers For Treatment of PTSD During Pregnancy

Обзор

The majority of women with perinatal posttraumatic stress disorder (PTSD) do not receive mental health treatment despite the documented associations between PTSD and adverse pregnancy outcomes; this is likely due to workforce shortages, lack of data on the effectiveness of existing evidence-based treatment for PTSD in usual care obstetrics settings, and patient-level barriers to engagement such as stigma. The proposed study is a randomized controlled trial, which will examine the effectiveness of a brief evidence-based treatment for PTSD (i.e., Written Exposure Therapy) during pregnancy and the non-inferiority of delivery of this treatment by community health workers vs. delivery by mental health clinicians.

Подробное описание

Pregnant women with posttraumatic stress disorder (PTSD) are at increased risk for adverse pregnancy outcomes, yet the majority of pregnant women with mental health needs do not receive treatment, with disparities in treatment utilization among low-income and racial and ethnic minority women. Perinatal mental health treatment gaps are foremost a consequence of behavioral health workforce shortages and a lack of data on PTSD treatment during pregnancy. Mental health stigma and medical mistrust due to racism further impact engagement in care. Written Exposure Therapy (WET) is a brief 5-session PTSD treatment that was designed to address the capacity-limiting concerns of first-line treatments (e.g., time burden of training and delivery). WET has demonstrated non-inferiority (and fewer dropouts) when compared to first-line PTSD treatments. As such, the empirical support and implementation advantages of WET suggest the promise of this intervention in addressing PTSD among pregnant women seen in usual care obstetrics settings. Training non-mental health specialists, such as community health workers (CHWs), to deliver WET may dually address workforce capacity challenges and patient engagement factors such as stigma. The objective of this research is to conduct a randomized controlled trial to examine both the effectiveness of WET for treatment of PTSD during pregnancy against an active control condition \[i.e., emotion focused supportive therapy (EFST)\] and the non-inferiority of WET delivery with a community health worker (CHW-WET) vs. WET delivery with a mental health clinician. A total of 240 pregnant women with PTSD receiving obstetrical care at Boston Medical Center (BMC), a large safety net hospital that cares for a racially and ethnically diverse population, will be recruited. Following a baseline visit, women will be randomized to either CHW-WET (N=80), standard WET (N=80), or EFST (N=80). Participants in either WET condition will receive 5 individual sessions focused on the use of writing to activate the trauma memory, process emotions, and make meaning. EFST participants will receive 5 individual sessions of supportive therapy. Participants will complete well-established measures of PTSD and other psychological symptoms (e.g., depression) and proposed moderators of treatment engagement at baseline, post-treatment, and 1-, 6-, and 12-months postpartum. Patients and providers will also complete measures and interviews following treatment to assess feasibility, acceptability, and appropriateness of the WET delivery approaches in a usual care setting. Aim 1 is to determine if a) CHW-WET is non-inferior to standard WET and b) CHW-WET has better retention than standard WET. Aim 2 is to demonstrate the effectiveness of WET for treatment of PTSD (vs. EFST) in an obstetrics setting. Exploratory Aim 3 will examine moderators of treatment engagement such as mental health stigma to inform a personalized approach to WET treatment delivery. Aim 4 is to conduct a process evaluation of the WET delivery approaches. This study will inform future efforts to improve access to and quality of care for treatment of PTSD during pregnancy.

Вмешательства

  • Поведенческое Written Exposure Therapy (WET)
    5 individual sessions that cover psychoeducation about PTSD, the rationale for exposure treatment, and directing patients to write in session for 30 minutes about their traumatic experience using scripted instructions. Each session includes unique writing instructions. Earlier sessions focus on describing the details of a traumatic stressor linked to their symptoms, with particular attention to felt emotions and thoughts. Later writing sessions focus on writing about the meaning of the traumatic
  • Поведенческое Emotion Focused Supportive Therapy (EFST)
    5 individual sessions where patients choose what problems to discuss in each session. Therapists validate and clarify patients' emotions and engage in problem solving during sessions.

Первичные конечные точки

  • Clinician Administered Scale for PTSD-5 (CAPS-5) at baseline [Срок оценки: baseline]
  • Clinician Administered Scale for PTSD-5 (CAPS-5) at 8 weeks [Срок оценки: 8 weeks]
  • Clinician Administered Scale for PTSD-5 (CAPS-5) at 1 month postpartum [Срок оценки: 1 month postpartum]
  • Clinician Administered Scale for PTSD-5 (CAPS-5) at 6 months postpartum [Срок оценки: 6 months postpartum]
  • Clinician Administered Scale for PTSD-5 (CAPS-5) at 12 months postpartum [Срок оценки: 12 months postpartum]
Вторичные конечные точки (8)
  • PTSD Checklist for DSM-5 (PCL-5) [Срок оценки: baseline, 8 weeks, 1 month postpartum, 6 months postpartum, 12 months postpartum]
  • Patient Health Questionnaire (PHQ-9) [Срок оценки: baseline, 8 weeks, 1 month postpartum, 6 months postpartum, 12 months postpartum]
  • Depression, Anxiety, and Stress Scale (DASS-21) - Anxiety Scale only [Срок оценки: baseline, 8 weeks, 1 month postpartum, 6 months postpartum, 12 months postpartum]
  • Number of study sessions attended [Срок оценки: 1 month postpartum]
  • Number of participants that completed all 5 study visits [Срок оценки: 1 month postpartum]
  • Inventory of Psychosocial Functioning (IPF) [Срок оценки: baseline, 8 weeks, 1 month postpartum, 6 months postpartum, 12 months postpartum]
  • Postpartum Bonding Questionnaire (PBQ) [Срок оценки: 1 month postpartum, 6 months postpartum, 12 months postpartum]
  • Client Satisfaction Questionnaire (CSQ-8) [Срок оценки: 8 weeks]

Критерии участия

Критерии включения

  • Pregnant woman receiving prenatal care at BMC Obstetrics and Gynecology (OB/GYN) Department
  • Presenting for prenatal care prior to gestational age of 28 weeks
  • Meet diagnostic or subthreshold criteria (i.e., endorsement of 3 out of the 4 symptom clusters) for PTSD on the Clinician Administered PTSD Scale for DSM-5 (CAPS-5)

Критерии исключения

  • Clinician judgment that the patient is not appropriate for outpatient level care (i.e., patient needs detox, inpatient, or residential treatment)
  • Current psychosis or unstable bipolar disorder diagnosis (determined via clinician-administered interview)
  • Currently receiving exposure-based PTSD treatment (e.g., WET, prolonged exposure, cognitive processing therapy) elsewhere
  • Current incarceration. Incarcerated individuals are only seen at BMC for obstetrical care and are not allowed to receive mental health care outside of their correctional facility

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
  • Boston Medical Center and remote — Boston

Идентификаторы

NCT: NCT05486793 · H-42619 · 1R01HD107282-01A1

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗