ISRCTN29401613进行中(未招募)未知
Improving outcomes for women diagnosed with early breast cancer through adherence to adjuvant endocrine therapy: the feasibility study
ewcastle upon Tyne Hospitals NHS Foundation Trust0 个研究点目标入组 90 人开始时间: 2022年8月12日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 90
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •Sub-study 1
- •The following patients will be eligible:
- •1. Aged 18 years old and over
- •3. Diagnosis of ER-positive invasive breast cancer
- •4. Medium or high risk of recurrence, defined as one of the following:
- •4.1. T2 and N0
- •4.2. T2 and N>0
- •4.3. T1 and N>0
- •4.4. T1 and N0 and grade 3
- •5. Within 3 months of first oral adjuvant endocrine therapy (AET) prescription (tamoxifen or aromatase inhibitor)
- •6. Completed surgery
- •7. Completed chemotherapy (if applicable)
- •8. Can access the internet and have an email address
- •9. Are willing to use a support package with a web-based component
- •Sub-study 2
- •The following patients will be eligible:
- •1. Aged 18 years old and over
- •3. Diagnosis of ER-positive invasive breast cancer
- •4. Medium or high risk of recurrence, defined as one of the following:
- •4.1. T2 and N0
- •4.2. T2 and N>0
- •4.3. T1 and N>0
- •4.4. T1 and N0 and grade 3
- •5. Were first prescribed oral AET (tamoxifen or aromatase inhibitor) within the past 9-36 months
- •6. Have completed surgery
- •7. Have completed chemotherapy (if applicable)
排除标准
- •Sub-study 1 and 2 exclusion criteria:
- •The following patients with early-stage ER+ve invasive breast cancer will be ineligible:
- •2. Have been prescribed adjuvant CDK4/6i (abemaciclib)
- •3. Have cognitive impairment sufficient to preclude participation, as judged by the clinical team
- •4. Are unable to read and understand English
- •5. Had previous AET (for another breast cancer)
- •6. Have not had surgery for breast cancer
研究者
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