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临床试验/NCT04553289
NCT04553289已完成不适用

Exercise Into Pain in Subacromial Shoulder Pain: a Randomized Controlled Trial

Universiteit Antwerpen1 个研究点 分布在 1 个国家目标入组 43 人开始时间: 2020年8月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
43
试验地点
1
主要终点
Shoulder Pain and Disability Index (SPADI)

研究概览

简要总结

The aim of the randomized clinical trial is to investigate if "exercising into pain" gives better results in term of clinical outcomes compared to a non-painful exercise program.

详细描述

Exercise therapy is the first choice of treatment in the treatment of subacromial shoulder pain (SSP). Guidelines suggest exercise therapy for at least three months and research underlines the importance of progressive loaded exercise therapy at high dosage. However, it is not clear which is the best type of exercise and if pain should be provoked or avoided during exercise. Recent research found that painful exercises are beneficial in short term on pain and function in patients with different kinds of chronic musculoskeletal pain. The aim is to investigate if one painful exercise can give better and faster results in the management of SSP than non-painful program.

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
Triple (Participant, Investigator, Outcomes Assessor)

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

  • shoulder pain for at least 3 months, elicited in the anterolateral shoulder region
  • at least 3 out of 5 of the following tests positive: Neer test, Hawkins-Kennedy, Jobe, painful arc, external resistance test
  • resting pain should be at 2/10 maximum on verbal numerical pain rating scale (NPRS)

排除标准

  • bilateral shoulder pain
  • corticosteroid injections 6 weeks prior to the study
  • pregnancy, inability to understand spoken or written Dutch
  • clinical signs of full-thickness rotator cuff tears (positive external and internal rotation lag tests and drop arm test)
  • evidence of adhesive capsulitis
  • previous cervical, thoracic or shoulder surgery; recent fractures or dislocations on the painful shoulder
  • primary complaint of spinal pain or signs of central nervous system involvement or signs of cervical nerve root involvement; reproduction of shoulder pain with cervical rotation or axial compression
  • primary diagnosis of acromioclavicular pathology, shoulder instability
  • a radiologically confirmed fracture or previous medical imaging confirming the presence of calcification larger than 5 mm
  • presence of competing pathologies (inflammatory arthritis, neurological disorders, fibromyalgia, malignancy, psychiatric illness, osteoporosis, hemophilia, rheumatic polymyalgia)
  • more than 4h of training in sport overhead shoulder activities per week

结局指标

主要结局

Shoulder Pain and Disability Index (SPADI)

时间窗: Change from baseline to 12 weeks

There are 13 items, divided in two subscales: pain (5 items) and function (8 items). Each item is scored from 0 (no pain/no difficulty) to 10 (worst imaginable pain/so difficult it requires help) on a NPRS. The final score is a percentage derived from an average of the two subscales, where higher score means worse outcome.

次要结局

  • Maximum Voluntary Contraction (MVC) in internal rotation, external rotation, scaption(Change from baseline to 6 months)
  • Scapular Correction(Change from baseline to 6 months)
  • Supraspinatus Tendon Thickness(Change from baseline to 6 months)
  • Visual Analogue Scale (VAS)(Change from baseline to 6 months)
  • Health-Related Quality of Life(Change from baseline to 6 months)
  • Fear-Avoidance Beliefs Questionnaire (FABQ)(Change from baseline to 6 months)
  • Scapular Dyskinesis(Change from baseline to 6 months)
  • Acromiohumeral Distance(Change from baseline to 6 months)
  • Fear of Pain Questionnaire (FPQ-9)(Change from baseline to 6 months)
  • Range of Movement (ROM) in internal rotation, external rotation, scaption(Change from baseline to 6 months)
  • Coracohumeral distance(Change from baseline to 6 months)
  • Subscapularis Tendon Thickness(Change from baseline to 6 months)
  • Shoulder Pain and Disability Index (SPADI)(Change from baseline to 6 months)

研究者

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

Filip Struyf

Professor

Universiteit Antwerpen

研究点 (1)

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