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临床试验/NCT05726643
NCT05726643尚未招募不适用

Effect of Kinesiotaping Augmented By Resistive Exercise on Fatigue, Physical Strength, Quality of Life in Breast Cancer Survivors

Cairo University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2023年2月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
40
试验地点
1
主要终点
Assessing the change in fatigue

研究概览

简要总结

The purpose of the study will be to investigate the effect of kinesotaping augmented by resistive exercise on fatigue, muscle strength, and QoL in breast cancer survivors.

详细描述

The present study will provide an evidence base to women's health care providers about the effect of strength training augmented by kinesotaping on fatigue, QoL and muscle strength in breast cancer women compared to strength training alone

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
Single (Investigator)

入排标准

年龄范围
40 Years 至 55 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Patient's age will range from 40- 55 years.
  • •Their body mass index (BMI) will be from 25 to 29,9 Kg/m
  • •They suffer from breast cancer.
  • •They will receive chemotherapy within previous 3 months.
  • •They complain from fatigue, deterioration in their daily living activity (ADL) and feeling of weakness in their muscles.

排除标准

  • •Respiratory or heart problems affecting mobility
  • •Marked skeletal deformity.
  • •Visual system affection.
  • •Cognition problems.
  • •Previous surgeries at their back and/or lower limbs.

研究组 & 干预措施

resistive training group

Active Comparator

consists of 20 patients who will receive resistive training for 2times per week for 12 weeks

干预措施: resistive training (Other)

kinesotaping group

Experimental

consists of 20 patients who will receive resistive training program augmented by kinesotaping, 2 times /week for 12 weeks.

干预措施: resistive training (Other)

kinesotaping group

Experimental

consists of 20 patients who will receive resistive training program augmented by kinesotaping, 2 times /week for 12 weeks.

干预措施: kinesiotaping (Other)

结局指标

主要结局

Assessing the change in fatigue

时间窗: at baseline and after 12 weeks of intervention

The Fatigue Severity Scale is a 14-item will be used to measure the severity, frequency and diurnal variation of fatigue, as well as its perceived interference with quality of life.

Assessing the change in quality of life

时间窗: at baseline and after 12 weeks of intervention

By using 36-Item Short Form (SF-36) health survey will be used to assess QoL. The SF-36 questionnaire includes eight multiple-item subscales that evaluate physical function, social functioning, role limitations due to physical problems and role limitations due to emotional problems, mental health, vitality, pain and general health perception. Total score on each SF-36 subscale ranges between 0 and 100. Greater score indicates better QoL

Assessing the change in muscle strength

时间窗: at baseline and after 12 weeks of intervention

Muscle strength will be assessed using dynamometer at starting and after 12 weeks of the treatment course.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Alaa Mos'ad Ebrahim Rmdan

Principal Investigator

Cairo University

研究点 (1)

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