跳至主要内容
临床试验/NCT03750864
NCT03750864已完成不适用

An Innovative Approach to Reduce Lung Cancer Stigma

University of Arizona3 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2018年10月27日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
24
试验地点
3
主要终点
Number of individuals who consent to the intervention

研究概览

简要总结

This is a feasibility study examining the feasibility and acceptability of a novel psychotherapy intervention on lung cancer patients who are experiencing stigma.

详细描述

Experiences of stigma (perception and internalization of negative appraisal and devaluation from others) are pervasive for lung cancer patients. Previous work has shown associations between lung cancer stigma and detriments in clinically relevant outcomes such as depression, lower quality of life, and reduced engagement in cancer care.

The investigators previously developed Acceptance and Commitment Therapy for Lung Cancer Stigma (ACT-LCS) as a patient-focused intervention to reduce the self-blame, guilt and inhibited disclosure associated with lung cancer stigma. ACT-LCS is based in Acceptance and Commitment Therapy (ACT), a cognitive-behavioral treatment that promotes psychological flexibility through acceptance and valued direction.

This is a feasibility study examining the feasibility and acceptability of ACT-LCS.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
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

  • Proficiency in English
  • Diagnosed with or treated for Non-Small Cell Lung Cancer (NSCLC) or Small Cell Lung Cancer (SCLC) within the prior 12 months.
  • Scores of 37.5 on the Lung Cancer Stigma Inventory (LCSI) screening measure

排除标准

  • Not proficient in English

结局指标

主要结局

Number of individuals who consent to the intervention

时间窗: 10 months

This measure will be calculated as a function of those eligible and approached who consented to the intervention. It will be utilized as a metric of feasibility and acceptability.

Number of sessions that each consented patient attended

时间窗: 10 months

This measure will be calculated as a count of sessions that each consented participant attended. It will be utilized as a metric of acceptability of the intervention among consented participants.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

Loading locations...

相似试验