跳至主要内容
临床试验/NCT06395506
NCT06395506招募中不适用

An Open-label Randomized Trial of Exercise ± Creatine Supplementation to Augment the Adaptations of Exercise Training in Cancer Survivors

The University of Texas Medical Branch, Galveston2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年10月29日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
2
主要终点
Change in physical functional capacity in breast cancer survivors

研究概览

简要总结

The study's purpose is to evaluate whether creatine supplementation can help breast cancer survivors respond quicker to exercise by improving strength, endurance, and body composition. We are seeking to compare information collected from healthy woman of the same age who have never had breast cancer to those participants who have had breast cancer and undergone chemotherapy treatment.

详细描述

The primary objective of this study is to determine the effects of creatine supplementation in modulating strength and physical function in breast cancer survivors that have recently completed chemotherapy. The primary objective is to determine the effects of creatine in modulating strength and physical function in cancer survivors.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(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

结局指标

主要结局

Change in physical functional capacity in breast cancer survivors

时间窗: baseline and 12 weeks

Determine the change in strength in breast cancer survivors by comparing pre and post measurements of the six minute walk test.

Change in strength in breast cancer survivors

时间窗: baseline and 12 weeks

Determine the change in strength in breast cancer survivors by comparing pre and post measurements of strength measurement tools including 1RM/10RM/Biodex evaluations.

次要结局

  • Change intramuscular storage of creatine(baseline and 12 weeks)
  • Change in the return of strength for breast cancer survivors with creatine + exercise(12 weeks)
  • Change in body composition in cancer survivors(baseline and 12 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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