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临床试验/NCT07190768
NCT07190768尚未招募不适用

The Comparison of the Effectiveness of Kinesiologic Taping and Dry Needling in the Treatment of Subacromial Pain Syndrome: a Randomize Trial

Bursa City Hospital0 个研究点目标入组 100 人开始时间: 2025年10月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
100
主要终点
Pain intensity (Visual Analogue Scale, VAS)

研究概览

简要总结

This study aims to compare the effectiveness of two common physiotherapy methods, Kinesiologic Taping (KT) and Dry Needling (DN), in the treatment of Subacromial Pain Syndrome (SAPS), a frequent cause of shoulder pain. The trial also investigates whether using KT and DN together provides greater benefits than using them separately. The main goal is to determine which treatment approach is more effective in reducing pain and improving shoulder function in patients with SAPS.

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
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-65 years
  • Pain in the upper, outer arm, especially during shoulder elevation
  • Shoulder pain lasting more than 6 weeks with or without partial rotator cuff tear
  • At least three of the following findings:
  • Painful arc during flexion or abduction
  • Positive Neer test
  • Positive Hawkins-Kennedy test
  • Painful resisted external rotation
  • Positive Jobe's test
  • Diagnosis confirmed by MRI evaluation when indicated

排除标准

  • Participation in a physical therapy program or receipt of injection therapy within the past 3 months
  • Previous shoulder surgery
  • Presence of joint contracture
  • Complete tendon rupture
  • Cervical radiculopathy
  • Systemic inflammatory disease (e.g., rheumatoid arthritis, ankylosing spondylitis)
  • Known allergy to tape or materials used in interventions
  • Bleeding disorders
  • Local infection or open wound in the treatment area
  • Cognitive dysfunction that prevents cooperation
  • History of malignancy

结局指标

主要结局

Pain intensity (Visual Analogue Scale, VAS)

时间窗: Baseline, immediately after first treatment, 1 week after first treatment, and at the end of week 3.

次要结局

  • Shoulder function (Quick-DASH questionnaire)(Baseline, 1 week after first treatment, and at the end of week 3.)
  • Kinesiophobia (Tampa Scale of Kinesiophobia, TSK-19)(Baseline, 1 week after first treatment, and at the end of week 3.)

研究者

发起方
Bursa City Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Erkan KAYA

Assoc. Prof

Bursa City Hospital

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