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临床试验/NCT01013233
NCT01013233Unknown不适用

Training of Cognitive Function of Patients After Chemotherapy

Charite University, Berlin, Germany1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2009年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
20
试验地点
1
主要终点
several cognitive tests (TAP, VLMT, TMT, Stroop, RWT, D2, LGT-3)

研究概览

简要总结

The purpose of this study is to improve cognitive dysfunction following chemotherapy, the investigators investigated to see whether a cognitive training for memory and concentration skills can improve cognitive performance in patients following cancer treatment.

详细描述

Patients following chemotherapy invited for a cognitive training. Before and after cognitive function will evaluate.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •patients with cancer 6 weeks after chemotherapy

排除标准

  • •patients with neurological or psychiatric disorders
  • •patients without compliance

研究组 & 干预措施

training

Experimental

Patients in this group start the cognitive training over 6 weeks directly after randomization.

干预措施: cognitive training (Behavioral)

control

Placebo Comparator

In this control group begin the training in a cross-over design 7 weeks after randomization.

干预措施: control group (Other)

结局指标

主要结局

several cognitive tests (TAP, VLMT, TMT, Stroop, RWT, D2, LGT-3)

时间窗: one weeks following the end of the cognitive training

次要结局

  • quality of life and subjective perception of cognitive problems(7 weeks)

研究者

申办方类型
Other

研究点 (1)

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