跳至主要内容
临床试验/NCT00237926
NCT00237926已完成不适用

Comparing Aerobic to Resistance Training in Recovery From Cancer

TriService Nursing Research Program2 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2005年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
58
试验地点
2
主要终点
quality of life

研究概览

简要总结

The purpose of this study is to compare the health outcomes of a 12-week exercise program focused on aerobic training (using a treadmill) to a 12-week exercise program focused on resistance training (using Thera-Bands) in sedentary patients within 6 months of completing treatment for cancer.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

入选标准

  • have a biopsy-proven cancer diagnosis
  • be within six months of having completed chemotherapy or radiation therapy for treatment for cancer as determined by the primary physician
  • be ambulatory but sedentary (i. e., has not followed an exercise regimen of a minimum of 3 times per week for at least 20 minutes each session over the previous six weeks)
  • have an Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 asymptomatic) or 1 (symptomatic, fully ambulatory)
  • be at least 18 years old
  • be able to read and speak English
  • have a medical statement from either the patient's primary care provider or the primary oncologist indicating that participation in the program is not medically contraindicated

排除标准

  • following an exercise regimen a minimum of 3 times per week for at least 20 minutes each session within the previous 6 weeks
  • bone or joint destruction that could be aggravated with exercise
  • severe cognitive impairment identified by either the patient's medical care provider or by the study team
  • neuropathy-sensory common toxicity criteria (CTC) grade 3 (sensory loss or paresthesia interfering with activities of daily living) or grade 4 (permanent sensory loss that interferes with function) peripheral neuropathy

结局指标

主要结局

quality of life

时间窗: 12-weeks

次要结局

  • exercise tolerance(12-weeks)

研究者

发起方
TriService Nursing Research Program
申办方类型
Other

研究点 (2)

Loading locations...

相似试验