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临床试验/NCT02773693
NCT02773693Unknown不适用

Treatment of Comorbid Sleep Disorders and Post Traumatic Stress Disorder (PTSD)

University of North Texas, Denton, TX2 个研究点 分布在 1 个国家目标入组 94 人开始时间: 2016年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
94
试验地点
2
主要终点
Clinician Administered PTSD Scale (CAPS-5)

研究概览

简要总结

The primary objective of the current study is to determine if providing cognitive-behavioral therapy of Insomnia and nightmares (CBTin) and Cognitive Processing Therapy of PTSD (CPT) results in greater PTSD and sleep symptom reduction than CPT only. A secondary objective is to determine if the sequencing of CBTl&N before or after CPT results in differential effects on PTSD and sleep symptom reduction.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Chronic Insomnia, as defined by the Diagnostic and Statistical Manual-fifth edition (DSM-5) (American Psychiatric Association, 2013) assessed with Structured Clinical Interview for DSM-5 Sleep Disorders (SCISD).
  • Chronic Nightmare Disorder, as defined by DSM-5, assessed with the SCISD.
  • PTSD, as defined by DSM-5, assessed by Clinician-Administered Posttraumatic Stress Scale-5 (CAPS-5).
  • Active duty military and recently discharged Veterans at Fort Hood eligible for treatment at Carl R. Darnall Army Medical Center (CRDAMC).
  • History of having deployed in support of combat operations following 9/11, assessed by self-report.
  • Stable on psychotropic and/or hypnotic medications and/or interventions for sleep (e.g., Continuous Positive Air Pressure for sleep apnea) administered by other providers for at least one month assessed by self-report and review of medical record.
  • Willing to refrain from new behavioral health or medication treatment for issues pertaining to sleep, PTSD, or nightmares during participation in the study.
  • Indication that the individual plans to be in the area for the 5 months following the first assessment.

排除标准

  • Individuals who have been re-deployed from a theater of operation less than 3 months.
  • Current suicide or homicide risk meriting crisis intervention as assessed by the Patient Health Questionnaire (PHQ-9), The Depressive Symptom Index - Suicidality Subscale (DSI-SS), or the Self-Injurious Thoughts and Behaviors Interview (SITBI).
  • Inability to speak and read English.
  • Moderate to severe brain damage, assessed by the inability to comprehend the baseline questionnaires.
  • Pregnancy, assessed by self-report and review of medical record, because sleep disturbances due to pregnancy may be the result of different mechanisms and the proposed instruments and treatments have not been validated in this population.
  • Current circadian rhythm, environmental, sleep deprivation, or hypersomnia sleep disorder, assessed by self-report because CBTin has not been validated in these populations.
  • Other untreated sleep disorders to include individuals with clinically significant obstructive sleep apnea (Respiratory Disturbance Index >5/hr), periodic limb movement disorder (PLMD; >15/hr with arousals), nocturnal seizures, or a parasomnia (e.g., sleepwalking, confusional arousals, nocturnal eating and drinking syndrome), based on criteria from the International Classification of Sleep Disorders-third edition (American Academy of Sleep Medicine, 2013). Individuals meeting criteria for one of the above sleep disorders will be seen for clinical care at the CRDAMC Sleep Center. Once the aforementioned sleep disorder is stably treated, individuals meeting the study criteria for insomnia, nightmares, and PTSD can be reassessed for participation in this study.
  • Sleep efficiency >85%, as assessed by the sleep diary.
  • Serious mental health diagnosis (e.g., bipolar disorder or psychosis) assessed with review of baseline questionnaires, review of medical record, and/or Mini International Neuropsychiatric Interview (MINI 7.0 Mania module).
  • Currently engaged in evidence-based psychotherapy for PTSD (i.e., Prolonged Exposure Therapy or Cognitive Processing Therapy) or Insomnia or nightmares (i.e., Cognitive Behavioral Therapy) by self-report and review of medical record.

研究组 & 干预措施

CPT

Active Comparator

Cognitive Processing Therapy-cognitive only version (typically labeled CPT-C, but labeled CPT in this grant for simplicity) is a type of Cognitive Therapy addressing daytime symptoms of PTSD. This arm will have 12 twice-weekly sessions, followed by 6 weekly sessions.

干预措施: Cognitive Processing Therapy-Cognitive Only (CPT) (Behavioral)

CPT

Active Comparator

Cognitive Processing Therapy-cognitive only version (typically labeled CPT-C, but labeled CPT in this grant for simplicity) is a type of Cognitive Therapy addressing daytime symptoms of PTSD. This arm will have 12 twice-weekly sessions, followed by 6 weekly sessions.

干预措施: Continuation Cognitive Processing Therapy-Cognitive Only (CPT) (Behavioral)

CBTin+CPT

Active Comparator

Cognitive Behavioral Therapy of Insomnia and nightmares (CBTin) will be used to address nighttime symptoms of PTSD during 6 weekly sessions, followed by 12 twice-weekly sessions of CPT.

干预措施: Cognitive Processing Therapy-Cognitive Only (CPT) (Behavioral)

CBTin+CPT

Active Comparator

Cognitive Behavioral Therapy of Insomnia and nightmares (CBTin) will be used to address nighttime symptoms of PTSD during 6 weekly sessions, followed by 12 twice-weekly sessions of CPT.

干预措施: Cognitive Behavioral Therapy of Insomnia and Nightmares (CBTin) (Behavioral)

CPT+CBTin

Active Comparator

12 twice-weekly sessions of CPT followed by 6 sessions of CBTin.

干预措施: Cognitive Processing Therapy-Cognitive Only (CPT) (Behavioral)

CPT+CBTin

Active Comparator

12 twice-weekly sessions of CPT followed by 6 sessions of CBTin.

干预措施: Cognitive Behavioral Therapy of Insomnia and Nightmares (CBTin) (Behavioral)

结局指标

主要结局

Clinician Administered PTSD Scale (CAPS-5)

时间窗: Change from baseline to 1-month post-treatment (i.e., after the completion of all 18 sessions, not to exceed 22 weeks from baseline).

The CAPS-5 (Weathers, Litz, et al., 2013) is a structured diagnostic interview and gold standard for assessing PTSD. The scale also assesses social and occupational functioning, dissociation, and the validity of symptom reports. The CAPS was revised to match DSM-5. The CAPS was revised to accommodate the changes made in DSM-5, to reduce administration time, and to facilitate learning administration and scoring procedures. The CAPS-5 will be the primary outcome of PTSD symptom severity.

次要结局

  • Sleep Diary Sleep Efficiency(Change from baseline to 1-month post-treatment (i.e., after the completion of all 18 sessions, not to exceed 22 weeks from baseline).)
  • PTSD Checklist -DSM-5 (PCL-5)(Change from baseline to 1-month post-treatment (i.e., after the completion of all 18 sessions, not to exceed 22 weeks from baseline).)

研究者

发起方
University of North Texas, Denton, TX
申办方类型
Other
责任方
Sponsor

研究点 (2)

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