NCT06618690进行中（未招募）不适用
Efficacy of a Supervised Exercise Program on Pain, Physical Function, and Quality of Life in Breast Cancer Survivors: Protocol for a Randomized Clinical Trial
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 325
- 试验地点
- 1
- 主要终点
- repeated measures ANOVA
研究概览
简要总结
The purpose of this project is to develop a randomized clinical trial to determine the efficacy of a supervised exercise program on pain, physical function and quality of life in female breast cancer survivors
详细描述
A randomized, double-blind, clinical trial will be conducted with 325 participants. The intervention group will receive a supervised exercise program for 12 weeks, while the control group will receive no intervention. Participants' pain, physical function and quality of life will be assessed at baseline, post-intervention and 12 weeks post-intervention.
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
- Double (Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •women between 18 and 65 years of age,
- •women with oncologic treatment completed less than 3 months ago,
- •women without metastasis,
- •women without pathologies that contraindicate exercise,
- •women who have agreed to sign the informed consent form
排除标准
- •not attending scheduled sessions to instruct on the exercises to be performed, - being part of other studies,
- •undergoing another type of therapy
- •pregnancy patients.
结局指标
主要结局
repeated measures ANOVA
时间窗: 12 weeks
the range of motion, tone and muscle strength of the group will be measured in 3 measures over the 12 weeks
次要结局
未报告次要终点
研究者
研究点 (1)
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