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临床试验/NCT07373925
NCT07373925尚未招募不适用

Effect of Kinesio Taping Versus Dry Cupping Therapy in Treatment of Thoracic Kyphosis: A Randomized Control Trial

Cairo University0 个研究点目标入组 48 人开始时间: 2026年2月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
48
主要终点
Pain Intensity Level

研究概览

简要总结

This study will be conducted to investigate the effect of Kinesio taping versus dry cupping therapy in the treatment of thoracic kyphosis

详细描述

Kyphosis is defined as an increase in the forward curvature of the spine that is seen along the sagittal plane. When the forward curvature becomes excessive, this is called hyperkyphosis. The curvature can be a normal variance when presented in the thoracic spine or in excess be a cause for instability and concern. The natural history of kyphosis is not exactly well known. Kinesio Taping (KT) stands out as one such modality proposed to manage musculoskeletal disorders (MSK) disorders. First developed in the 1970s by Dr. Kenzo Kase, It is touted for pain relief, increased range of motion (ROM), and muscle relaxation. As such, it is widely used, not only among athletes but also in clinical medicine Another traditional technique is known as dry cupping therapy that involve the application of cups to create localised negative pressure on the skin, has been utilised for over four thousand years. Its use spans various conditions, including musculoskeletal pain. Dry Cupping has traditionally carried folkloric, cultural, religious, and spiritual significance within various societies It is used for health promotion, prophylaxis and treatment of a variety of diseases around the world. It is a well-recognized traditional method for managing medical conditions. Currently, the scope of cupping therapy is expanding, and a growing body of research is providing additional evidence-based data for the further advancement of this therapy in the treatment of a variety of diseases. It has gained popularity and acceptance as a method of treating pain as well as sports injuries and other medical conditions.

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 (Outcomes Assessor)

盲法说明

sealed envelopes

入排标准

年龄范围
18 Years 至 30 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects with thoracic kyphosis angle > 40° diagnosed by a medical doctor will be selected from Damietta University's clinic of physical education faculty.
  • Subjects from both genders with an age range between 18 and 30 years .
  • Subjects who are physically active in physical education sessions

排除标准

  • Subjects with medical conditions that restrict activity.
  • Those who received exercise intervention for kyphosis.
  • Structural thoracic kyphosis, defined as thoracic kyphosis that did not partially or completely disappear during prone extension, as assessed by a physical therapist.
  • Medical history of spinal fracture, spinal surgery, shoulder joint injury or pelvic injury.
  • Other spinal diseases; presence of scoliosis on Adam's forward bend test.
  • Spinal kyphosis due to visible thoracic deformity.
  • Subjects undergoing professional sports training.
  • Skin disease (dermatitis, psoriasis), neurological disease or cancer.
  • Using anticoagulants or nonsteroidal antidepressants.
  • Inflammatory or rheumatologic disorders of the spine.
  • Severe cardiopulmonary disease, rheumatic disease or pregnancy.
  • Have a pacemaker or metal implants.
  • Do not understand the written consent form.

研究组 & 干预措施

Kinesio taping

Experimental

16 participants will receive Kinesio taping once a week for 4 weeks + traditional treatment

干预措施: Kinesio taping (Other)

Kinesio taping

Experimental

16 participants will receive Kinesio taping once a week for 4 weeks + traditional treatment

干预措施: Conventional treatment (Other)

Dry Cupping Therapy

Experimental

16 participants will receive Dry Cupping Therapy 3 times a week for 4 weeks + traditional treatment

干预措施: Dry Cupping Therapy (Other)

Dry Cupping Therapy

Experimental

16 participants will receive Dry Cupping Therapy 3 times a week for 4 weeks + traditional treatment

干预措施: Conventional treatment (Other)

Conventional treatment

Active Comparator

16 participants will receive traditional treatment

干预措施: Conventional treatment (Other)

结局指标

主要结局

Pain Intensity Level

时间窗: up to 4 weeks

A visual analogue scale (VAS) will be used to measure the intensity of pain. With a score of 0 for no pain and 10 for the worst pain ever, this psychometric response scale, which measures pain intensity based on numerical values, is 10 cm or 100 mm in length. The interclass correlation ranges for the VAS, a validated and dependable measure of pain intensity, are 0.95 to 0.98. Patients rated their level of pain as mild if they scored 3.4 or less, moderate if they scored 3.5 to 7.4, and severe if they scored 7.5 or higher.

次要结局

  • Thoracic-curve angle(up to 4 weeks)

研究者

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

Aya Alaa Eldeen Sultan

Principal investigator: Aya Alaa Eldeen Sultan

Cairo University

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