An Adjunctive Family Intervention for Individual Posttraumatic Stress Disorder Treatment
An Adjunctive Family Intervention for Individual PTSD Treatment
研究概览
详细说明
The investigators will enroll pairs of Veterans and one adult family member who lives with them. Veterans will be beginning a course of PTSD-focused treatment at the Boston VA; Veterans' treatment will not be limited or changed by their participation in this study.
Family members will receive or not receive (depending on which Phase of the study they are recruited in) the BFI. The BFI consists of 2 sessions in which the family member meets one-on-one with a clinician to discuss PTSD, PTSD treatment, and how families can be most helpful to patients in treatment.
Veterans and family members will also be interviewed about their opinions and experiences regarding family-inclusive treatment for PTSD. Clinicians will be recruited and enrolled to obtain their information and feedback (via qualitative interviews), and to deliver the intervention in Phase II.
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
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Massachusetts
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Boston、Massachusetts、美国、02130
- VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Veterans must have a diagnosis of PTSD and be beginning a course of Prolonged Exposure (PE) or Cognitive Processing Therapy (CPT) at the Boston VA.
- Must also have an eligible family member who is willing to participate.
Exclusion Criteria:
- Current diagnosis of unstable bipolar disorder, substance dependence, past or present psychosis, or organic mental disorder
- Clear and current suicidal risk
- Current participation in family/couples therapy
学习计划
研究是如何设计的？
设计细节
- 主要用途：治疗
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的：Brief family intervention
Participants will receive the BFI in this arm of the study.
The BFI is a 2-session intervention for family members of Veterans who are beginning PTSD treatment.
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Two 50-minute sessions aimed at helping family members be most supportive to their loved one's treatment goals.
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无干预：No intervention
Participants will not receive the BFI in this arm of the study.
They will be eligible for any usual support or programming for the families of Veterans.
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研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Clinician-Administered PTSD Scale, 5th Edition
大体时间：16 weeks
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A measure of PTSD severity and diagnostic status.
Min value = 0, max value = 80.
Higher scores mean worse outcome.
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16 weeks
|
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Treatment Attendance/Dropout
大体时间：16 weeks
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A measure of Veterans' treatment attendance or premature dropout.
Data represents the Veterans who dropped out of their standard-care PTSD treatment.
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16 weeks
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Significant Others' Responses to Trauma Scale (SORTS)
大体时间：16 weeks
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A measure of self-reported family accommodation of PTSD symptoms.
Min value = 0, max value = 112.
Higher scores mean worse outcome.
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16 weeks
|
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Revised Dyadic Adjustment Scale
大体时间：16 weeks
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A measure of relationship quality.
Min value = 0, max value = 69.
Higher scores mean better outcome.
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16 weeks
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合作者和调查者
调查人员
- 首席研究员：Johanna Thompson-Hollands, PhD、VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- MHBB-013-16F
- IK2CX001589 (美国 NIH 拨款/合同)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)？
IPD 计划说明
IPD 共享时间框架
IPD 共享访问标准
IPD 共享支持信息类型
- 研究方案
- 国际碳纤维联合会
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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