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临床试验/NCT06701591
NCT06701591已完成不适用

Efficacy of Combined Kinesio-Taping With Chest Physiotherapy Program on Pain, Pulmonary Function, Respiratory Muscle Strength and Quality of Life After Mastectomy: A Randomized Controlled Trial

Cairo University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年12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
已完成
入组人数
60
试验地点
1
主要终点
visual analogue scale

研究概览

简要总结

The modified radical mastectomy (MRM) is a major surgical approach that necessitates the dissection of axillary lymph nodes. As a result, there is more bleeding and the treatment takes longer time. This treatment is used to treat locally advanced breast cancer. Numerous factors, including pain and respiratory depression from general anaesthesia, can impair respiratory function during the post-operative period. Pain causes the thoracic cage's post-operative movement to be restricted and the breathing muscles to become inhibited.

详细描述

KT is a new technology that is being used in the treatment of post-surgical and respiratory problems, among other innovative evidence-based therapeutic options in patient care. Recently, this method is useful for treating a variety of sports-related and musculoskeletal disorders, as well as pain management. According to a small body of research on the usefulness and efficacy of KT in treating respiratory conditions in patients with chronic obstructive pulmonary disease (COPD), it can lead to improvements in respiratory muscle strength and pulmonary function.

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
Double (Participant, Care Provider)

入排标准

年龄范围
30 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Females aged between 30 and 50 years
  • •Participants after modified radical mastectomy
  • •Participants able to comprehend instructions.
  • •Cooperative participants, and willing to participate in the study.

排除标准

  • •Participants having sensitive skin, scars, or lesions.
  • •Participants with unhealed incisions at the site of application.
  • •Participants with uncontrolled diabetes.
  • •Participants with deep vein thrombosis.
  • •Participants with previous chest diseases.
  • •Pregnancy.
  • •Participants with altered sensations.
  • •Participants with allodynia.
  • •Participants with active infection.

研究组 & 干预措施

Group A (Kinesiotaping group)

Experimental

Participants will be seated on a chair, KT will be applied bilaterally at the end of the expiration on the fifth to sixth and ninth to tenth intercostal muscles transversally and on the anterior and posterior axillary line longitudinally with 50% tension. In order to stimulate the muscle and support the function, the stimulation technique is usually applied from the origin to the insertion of the muscle with the recommended stretching of 25 to 50%.

Additionally, traditional physical therapy program will be conducted to participants in the study group.

干预措施: Kinesiotaping (Other)

Group A (Kinesiotaping group)

Experimental

Participants will be seated on a chair, KT will be applied bilaterally at the end of the expiration on the fifth to sixth and ninth to tenth intercostal muscles transversally and on the anterior and posterior axillary line longitudinally with 50% tension. In order to stimulate the muscle and support the function, the stimulation technique is usually applied from the origin to the insertion of the muscle with the recommended stretching of 25 to 50%.

Additionally, traditional physical therapy program will be conducted to participants in the study group.

干预措施: chest physical therapy (Other)

Group B (control group)

Active Comparator

They will receive the chest physical therapy program which is consisted of deep breathing exercises, postural drainage, cough, 3 times /week for 4 weeks.

干预措施: chest physical therapy (Other)

结局指标

主要结局

visual analogue scale

时间窗: 4 weeks

The visual representation of the pain range that a patient thinks they might experience is called a linear scale. The score is ranged from 0 to 10. The least the score, the better results. While, the higher the score, the worst the results.

次要结局

  • forced expiratory volume at first second (FEV1)(4 weeks)
  • Forced expiratory volume at first second /Forced vital capacity ratio.(4 weeks)
  • Forced vital capacity (FVC)(4 weeks)
  • Respiratory muscle strength(4 weeks)
  • Quality of life(4 weeks)

研究者

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

Nesma Morgan Allam

Assistant Professor of physical therapy for surgery, Faculty of physical therapy

Cairo University

研究点 (1)

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