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临床试验/NCT05457985
NCT05457985招募中不适用

Testing Adaptive Interventions to Improve Posttraumatic Stress Disorder (PTSD) Treatment Outcomes in Federally Qualified Health Centers

University of Michigan26 个研究点 分布在 1 个国家目标入组 430 人开始时间: 2022年6月23日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
430
试验地点
26
主要终点
Change in PTSD symptoms as measured by the Clinician-Administered PTSD Scale for Diagnostic and Statistical Manual of Mental Disorders (DSM)-5 (CAPS-5)

研究概览

简要总结

This trial is being completed to develop a stepped-care talk therapy model for patients with PTSD. Specifically, this study is testing whether beginning with one type of therapy is better than beginning with another type of therapy, and whether moving to a different therapy after four sessions is more helpful than staying with the same therapy, depending on how well it is working.

The central hypothesis is that beginning with a low- or medium-intensity PTSD intervention and then titrating intensity based on early indications of response will result in clinically significant PTSD symptom reduction with parsimony of resources.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

The primary outcome, the Clinician-Administered PTSD Scale (CAP-5), will be administered by a blinded study team member.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Receive care at a participating federally qualified health center (FQHC)
  • Have a Posttraumatic Stress Disorder checklist (PCL-5) score greater or equal (≥) to 33
  • Own a mobile device that can be used for the PTSD Coach App
  • Have had psychotropic medication stability for at least 4 weeks

排除标准

  • Severe cognitive impairment that in the judgment of the investigators makes it unlikely that the participant can adhere to the study regimen (as evidenced by confusion, inability to track discussion or answer questions, or other clear and significant indicators of cognitive impairment)
  • High risk of suicide (defined as meeting criteria for Action Step 3 on the Participant Suicide Risk Screening form
  • Severe alcohol or substance use disorder (moderate-severe alcohol use disorder on Alcohol Use Disorders Identification Test (AUDIT) (scores ≥ 15) or high risk on National Institute on Drug Abuse Quick Screen (scores ≥ 27))
  • Active psychosis or unmanaged bipolar disorder
  • Unstable housing
  • Current engagement in a trauma-focused behavioral treatment (such as Prolonged Exposure or Cognitive Processing Therapy).
  • Patients who do not speak English will be excluded for logistical reasons.

研究组 & 干预措施

Prolonged Exposure for Primary Care (PE-PC) then continue as early responder

Experimental

PE-PC consists of four weekly 30-minute sessions. At the 4th session or 9-week assessment point (whichever comes first), early responders will step down to every-other-week sessions for the duration of the second stage (for 8 weeks).

干预措施: Prolonged Exposure for Primary Care (PE-PC) (Behavioral)

Prolonged Exposure for Primary Care (PE-PC) then full PE

Experimental

PE-PC consists of four weekly 30-minute sessions. At the 4th session or 9-week assessment point (whichever comes first), slow responders that are then randomized to full PE and will have sessions once a week for eight weeks. During these 60-minute sessions, participants will practice in vivo and imaginal exposure and continue these exposure exercises every day at home.

干预措施: Prolonged Exposure for Primary Care (PE-PC) (Behavioral)

Prolonged Exposure for Primary Care (PE-PC) then full PE

Experimental

PE-PC consists of four weekly 30-minute sessions. At the 4th session or 9-week assessment point (whichever comes first), slow responders that are then randomized to full PE and will have sessions once a week for eight weeks. During these 60-minute sessions, participants will practice in vivo and imaginal exposure and continue these exposure exercises every day at home.

干预措施: Full Prolonged Exposure (Behavioral)

Clinician Supported PTSD Coach App then full PE

Experimental

During the first stage of treatment, participants will receive four weekly clinician support sessions or 9 weeks (whichever occurs first), slow responders that are then randomized to full PE will have sessions once a week for eight weeks. During these 60 minute sessions, participants will practice in vivo and imaginal exposure and continue these exposure exercises every day at home.

干预措施: Full Prolonged Exposure (Behavioral)

Clinician Supported PTSD Coach App then full PE

Experimental

During the first stage of treatment, participants will receive four weekly clinician support sessions or 9 weeks (whichever occurs first), slow responders that are then randomized to full PE will have sessions once a week for eight weeks. During these 60 minute sessions, participants will practice in vivo and imaginal exposure and continue these exposure exercises every day at home.

干预措施: Clinician Supported PTSD Coach App (Behavioral)

Prolonged Exposure for Primary Care (PE-PC) then continued PE-PC

Experimental

PE-PC consists of four weekly 30-minute sessions. At the 4th session or 9-week assessment point (whichever comes first), slow responders that are then randomized to continue with PE-PC (medium intensity) will continue weekly sessions for 8 weeks.

干预措施: Prolonged Exposure for Primary Care (PE-PC) (Behavioral)

Clinician Supported PTSD Coach App then continued CS PTSD Coach App

Experimental

During the first stage of treatment, participants will receive four weekly clinician support sessions or 9 weeks (whichever occurs first), slow responders that are then randomized to continue this treatment will have the frequency reduced to twice monthly.

干预措施: Clinician Supported PTSD Coach App (Behavioral)

Clinician Supported (CS) PTSD Coach App then continue as early responder

Experimental

During the first stage of treatment, participants will receive four weekly clinician support sessions or 9 weeks (whichever occurs first). Early responders will be encouraged to continue app use but will discontinue clinician support sessions for the remaining 8 weeks.

干预措施: Clinician Supported PTSD Coach App (Behavioral)

结局指标

主要结局

Change in PTSD symptoms as measured by the Clinician-Administered PTSD Scale for Diagnostic and Statistical Manual of Mental Disorders (DSM)-5 (CAPS-5)

时间窗: Baseline, 3-months

The CAPS-5 is a clinician-rated PTSD rating scale consisting of 30 items; the total score is calculated as the sum of 20 items assessing the 20 DSM-5 PTSD symptoms. These symptom items are scored on a 5-point scale from 0 (absent) to 4 (extreme/incapacitating). The total score of the 20 items ranges from 0 to 80 with higher scores indicating more severe PTSD symptoms. Therefore, a decrease in the total score indicates symptom improvement.

次要结局

  • Change in depressive symptoms measured by the Patient Health Questionnaire (PHQ-9)(Baseline, 3-months)
  • Change in quality of life and functioning measured by the EuroQol-5 Domain (EQ-5D-5L)(Baseline, 3-months)
  • Change in PTSD symptoms by the PTSD Checklist (PCL-5)(Baseline, 3-months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Rebecca Sripada

Associate Professor of Psychiatry

University of Michigan

研究点 (26)

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