跳至主要内容
临床试验/NCT02760524
NCT02760524已完成不适用

Desensitizing Distressing Recollections in Cancer Patients

Sidney Kimmel Cancer Center at Thomas Jefferson University2 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2010年4月11日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
44
试验地点
2
主要终点
Post traumatic Cognitions Inventory

研究概览

简要总结

The major goal of this study is to determine whether Neuro-Emotional Technique is a viable treatment option for decreasing distress in cancer patients. The potential advantages of NET are: 1) it is designed specifically to address distressing stimuli and unresolved emotional memories; 2) it is a brief, time-limited intervention; and 3) its multi-modal design may appeal to and benefit a broader range of patients than a single mode intervention

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
None

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

  • Age ≥18 years of age
  • Distressing cancer-related recollection that has persisted for at least six months
  • Distressing cancer-related recollection that causes physiological reactivity (i.e., increased heart rate and/or increased skin conductance level - SCL), as described in section 4.2.
  • Received a cancer diagnosis at least 6 months prior to being contacted for participation in this study

排除标准

  • Any current Major Mental Disorder, as assessed by Structured Clinical Interview for DSM IV Axis I Disorders (SCID - Clinical Version, First et al, 1997)
  • History of Post-traumatic Stress Disorder
  • Current active mood primary disorder prior to the cancer diagnosis (as per PI or designate)
  • History or current diagnosis of substance or alcohol abuse or dependence (as per PI or designate)
  • Use of psychotropic medications within the past month or current use of medications that would interfere with autonomic nervous system measures (benzodiazepines, barbiturates, major tranquilizers).
  • Use of some psychotropic medications are allowed such as SSRIs and certain sleep aids, but dosages must be stable from six weeks prior to enrollment and throughout study period
  • Any psychological or musculoskeletal problems that would interfere with psychophysiological assessments and treatment
  • Currently receiving chemotherapy or radiation
  • Are in the terminal stages of illness

研究组 & 干预措施

Intervention

Experimental

Subjects will receive NET intervention treatment immediately

干预措施: NET Intervention (Behavioral)

Control

Active Comparator

Subjects will receive NET intervention treatment and serve as a wait-list control

干预措施: NET Intervention (Behavioral)

结局指标

主要结局

Post traumatic Cognitions Inventory

时间窗: baseline/ 4 weeks/6 months follow up

change from baseline Post Traumatic Cognitions Inventory score

State Trait Anxiety Inventory

时间窗: baseline/4 weeks/6 months follow up

change from baseline State Trait Anxiety Inventory score

Brief Symptom Inventory

时间窗: baseline/4 weeks/6 month follow up

change from baseline Brief Symptom Inventory

次要结局

  • Autonomal response to distressing recollections(baseline/4 weeks follow up)
  • Genomic testing(baseline/ 4 weeks follow up)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验