ACTRN12618001615279已完成未知
Clinician Intervention to Reduce Fear of Recurrence in Cancer Survivors (CIFeR Study)
Psycho-Oncology Cooperative Group0 个研究点目标入组 61 人开始时间: 2018年10月2日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 61
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Educational / counselling / training
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- Female
入选标准
- •1)Women aged 18 years and above with histologically confirmed early stage (I-III inclusive) breast cancer who have undergone treatment with curative intent
- •2)Completed surgery and adjuvant chemotherapy/radiotherapy (where appropriate) greater than or equal to 6 months from time of registration (but may be on adjuvant hormone therapy)
- •3)Willing and able to complete study requirements including patient-rated outcome (PRO) surveys without assistance or translation
- •4)Completed signed written informed consent
排除标准
- •1)Current severe major depression (as defined by >15 on DASS-21) and anxiety (>21 on DASS-21)
- •2)Current psychotic illness or other psychiatric/cognitive condition that would impair the ability to participate in the intervention (as judged by the treating clinician)
- •3)Patients who are unable to understand written or spoken English
- •4)Objective evidence of recurrence or metastatic cancer of any type, as determined by the treating oncologist.
研究者
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