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临床试验/NCT07610499
NCT07610499尚未招募不适用

Creating Opportunities For Personal Empowerment (COPE) In Women With Breast Cancer During First-Line Therapy: A Pilot Randomized Controlled Trial

M.D. Anderson Cancer Center1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年10月30日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
40
试验地点
1

研究概览

简要总结

To learn if the Creating Opportunities for Personal Empowerment (COPE) intervention is feasible, acceptable, and helpful (compared to usual care) in women with breast cancer who are receiving first line treatment.

详细描述

Primary Objectives The primary objective of this study is to assess the feasibility and acceptability of the COPE intervention, a nurse-led cognitive-behavioral skills-building intervention, in women undergoing their first line of treatment for breast cancer.

  • The primary endpoint of feasibility will be evaluated by the percentage of participants in the intervention arm who completes at least five of the seven intervention sessions. If at least 70% of the intervention group participants complete five or more intervention sessions, the COPE intervention will be deemed feasible in women undergoing their first line of treatment for breast cancer.
  • The primary endpoint of acceptability will be evaluated by an investigator-developed instrument, the Acceptability of COPE in Breast Cancer Intervention Survey, The COPE intervention will be evaluated as acceptable if ≥50% of participants report that the intervention increased their ability to cope with their breast cancer diagnosis in their response to Question 1, "The COPE sessions affected my ability to cope with my breast cancer diagnosis in the following way: A) Increased my ability to cope with my breast cancer diagnosis: B) Decreased my ability to cope with my breast cancer diagnosis; or C) No change in my ability to cope with my breast cancer diagnosis."

研究设计

研究类型
Interventional
分配方式
Randomized
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
Female
接受健康志愿者

入选标准

  • Eligibility Criteria
  • Age 18 years and older
  • Diagnosed with stage I-III breast cancer
  • Receiving first line treatment for breast cancer
  • Receiving treatment at MD Anderson
  • Able to read, speak, and consent in English
  • Able to understand and be willing to sign a written informed consent document
  • Able to complete the study questionnaires and intervention sessions

排除标准

  • Diagnosed with multiple tumor types
  • Diagnosed with stage IV breast cancer
  • Unable to provide consent, such as cognitively impaired individuals
  • Has a preexisting psychiatric diagnosis (e.g., bipolar depression)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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