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临床试验/NCT06388304
NCT06388304已完成不适用

Pilot Study of Positive Affect Training for Endocrine Therapy Medication Adherence

Joanna Arch2 个研究点 分布在 1 个国家目标入组 39 人开始时间: 2024年3月12日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
39
试验地点
2
主要终点
Client Satisfaction Survey

研究概览

简要总结

The purpose of this study is to pilot and refine an online behavioral intervention based on Positive Affect Training (PAT) that aims to increase positive emotional attitudes and decrease negative emotional attitudes toward endocrine therapy (ET, i.e., anti-hormonal medication) and to increase positive affect and decrease negative affect more generally, among post-treatment breast cancer survivors who are prescribed ET to prevent recurrence of breast cancer.

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
21 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • hormone receptor-positive breast cancer stages 0-3
  • have finished primary treatment (chemotherapy/radiation/surgery)
  • are prescribed endocrine therapy (ET) currently or within the last two years
  • score above specified cut off (range, 0-10) on any of three questions:
  • How upset are you by having to take anti-hormonal therapy
  • How bothered are you by the side effects?
  • How difficult is it for you to take your anti-hormonal medication every day?
  • have internet access to complete online assessments and intervention components or agree to use and return a study wifi-activated iPad.

排除标准

  • metastatic disease
  • Individuals who are unable to interact with the intervention as needed. This includes those who are extremely visually impaired to the degree that they cannot see the screen and interact as required and individuals who cannot read and/or write in English. This is due to the nature of the intervention itself. If a participant is unable to interact with THRIVE as required, they are unlikely to benefit from the intervention or offer insightful feedback that can be used in refining the program.

结局指标

主要结局

Client Satisfaction Survey

时间窗: 1 week after completing the intervention

Satisfaction and feedback on THRIVE intervention

Acceptability of THRIVE intervention (AIM)

时间窗: 1 week after completing the intervention

Acceptability of Implementation Measure (Weimer et al., 2017)

Feasibility of THRIVE intervention

时间窗: 1 week after completing the intervention

Feasibility of Intervention Measure (Weimer et al., 2017)

次要结局

未报告次要终点

研究者

发起方
Joanna Arch
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Joanna Arch

Principal Investigator

University of Colorado, Boulder

研究点 (2)

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