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临床试验/NCT07191496
NCT07191496终止不适用

Quality of Life in Breast Cancer Survivors Who Were Pregnant During Their Cancer Treatment

M.D. Anderson Cancer Center1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年10月1日最近更新:

试验速览

阶段
不适用
状态
终止
入组人数
30
试验地点
1
主要终点
QOL Questionnaires

研究概览

简要总结

To assess the quality of life for women who were pregnant during their breast cancer treatment.

详细描述

Primary Objectives Provide preliminary data to describe the current QOL of breast cancer survivors who received cancer treatment while pregnant.

Secondary Objectives Identify the relationship between QOL and anxiety, depression, fear of cancer recurrence, and social support in breast cancer survivors, who received treatment while pregnant.

研究设计

研究类型
Observational
观察模型
Case Crossover
时间视角
Cross Sectional

入排标准

性别
Female
接受健康志愿者

入选标准

  • Eligibility Criteria
  • Female, any current age and any age at diagnosis
  • Documented diagnosis of breast cancer during pregnancy
  • Documentation of receiving chemotherapy during pregnancy
  • Alive with no evidence of disease at time of recruitment
  • Able to reach and speak English

排除标准

  • Any woman who delayed and received their chemotherapy after delivery.
  • Any woman who was diagnosed with breast cancer before or after their pregnancy.
  • Any woman whom there is documentation of inability to provide consent in the medical record

结局指标

主要结局

QOL Questionnaires

时间窗: Through study completion; an average of 1 year

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 (1)

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