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临床试验/NCT00343616
NCT00343616已完成3 期

Investigating Cognitive Function for Patients Participating in the BIG Trial 1-98 in Select Centers

ETOP IBCSG Partners Foundation24 个研究点 分布在 6 个国家目标入组 135 人开始时间: 2005年4月最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
入组人数
135
试验地点
24
主要终点
Objective cognitive function as measured by the CogState battery

研究概览

简要总结

RATIONALE: Studying cognitive function, such as thinking, attention, concentration, and memory, in postmenopausal women receiving hormone therapy for breast cancer may help improve quality of life and the ability to plan treatment for cancer.

PURPOSE: This phase III trial is studying cognitive function in postmenopausal women with breast cancer receiving hormone therapy on clinical trial IBCSG-1-98.

详细描述

OBJECTIVES:

Primary

  • Compare cognitive function in postmenopausal women with breast cancer who have received 5 years of adjuvant tamoxifen vs letrozole on protocol IBCSG-1-98.

Secondary

  • Compare cognitive function in patients who have received a single hormonal therapy for 5 years vs those who have received that same hormonal therapy for 3 years, having previously received an alternate hormonal therapy for 2 years.
  • Compare improvement in cognitive function 1 year after cessation of adjuvant hormonal therapy.
  • Compare changes in cognitive function in patients who have received prior adjuvant chemotherapy vs those who have not received adjuvant chemotherapy.
  • Assess the relationship between objective and subjective measures of cognitive function, including specific cognitive domains.
  • Assess the relationship between cognitive function and psychological distress, fatigue, and quality of life.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
30 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Tamoxifen for 5 years

Experimental

Patients treated with tamoxifen for 5 years after randomization.

干预措施: cognitive assessment (Procedure)

Letrozole for 5 years

Experimental

Patients treated with letrozole for 5 years after randomization.

干预措施: fatigue assessment and management (Procedure)

Tamoxifen for 5 years

Experimental

Patients treated with tamoxifen for 5 years after randomization.

干预措施: fatigue assessment and management (Procedure)

Tamoxifen for 5 years

Experimental

Patients treated with tamoxifen for 5 years after randomization.

干预措施: psychologic distress (Procedure)

Tamoxifen for 5 years

Experimental

Patients treated with tamoxifen for 5 years after randomization.

干预措施: quality-of-life assessment (Procedure)

Letrozole for 5 years

Experimental

Patients treated with letrozole for 5 years after randomization.

干预措施: cognitive assessment (Procedure)

Letrozole for 5 years

Experimental

Patients treated with letrozole for 5 years after randomization.

干预措施: psychologic distress (Procedure)

Letrozole for 5 years

Experimental

Patients treated with letrozole for 5 years after randomization.

干预措施: quality-of-life assessment (Procedure)

Tamoxifen 2 years plus letrozole 3 years

Experimental

Patients treated with tamoxifen for 2 years and afterwards with letrozole for 3 years.

干预措施: cognitive assessment (Procedure)

Tamoxifen 2 years plus letrozole 3 years

Experimental

Patients treated with tamoxifen for 2 years and afterwards with letrozole for 3 years.

干预措施: fatigue assessment and management (Procedure)

Tamoxifen 2 years plus letrozole 3 years

Experimental

Patients treated with tamoxifen for 2 years and afterwards with letrozole for 3 years.

干预措施: psychologic distress (Procedure)

Tamoxifen 2 years plus letrozole 3 years

Experimental

Patients treated with tamoxifen for 2 years and afterwards with letrozole for 3 years.

干预措施: quality-of-life assessment (Procedure)

Letrozole for 2 years plus tamoxifen for 3 years

Experimental

Patients treated with letrozole for 2 years and afterwards with tamoxifen for 3 years.

干预措施: cognitive assessment (Procedure)

Letrozole for 2 years plus tamoxifen for 3 years

Experimental

Patients treated with letrozole for 2 years and afterwards with tamoxifen for 3 years.

干预措施: fatigue assessment and management (Procedure)

Letrozole for 2 years plus tamoxifen for 3 years

Experimental

Patients treated with letrozole for 2 years and afterwards with tamoxifen for 3 years.

干预措施: psychologic distress (Procedure)

Letrozole for 2 years plus tamoxifen for 3 years

Experimental

Patients treated with letrozole for 2 years and afterwards with tamoxifen for 3 years.

干预措施: quality-of-life assessment (Procedure)

结局指标

主要结局

Objective cognitive function as measured by the CogState battery

时间窗: 6 years after randomization

次要结局

  • Fatigue as measured by the Brief Fatigue Inventory (BFI)(6 years after randomization)
  • Quality of life as measured by the IBCSG QL Core Form(6 years after randomization)
  • Subjective cognitive function as measured by the Cognitive Failures Questionnaire (CFQ)(6 years after randomization)
  • Psychological distress as measured by the General Health Questionnaire (GHQ)(6 years after randomization)

研究者

申办方类型
Network
责任方
Sponsor

研究点 (24)

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