跳至主要内容
临床试验/NCT01753271
NCT01753271已完成不适用

Subacute Effects of Cervicothoracic Spinal Manipulation in Addition to Shoulder Manual Therapy Plus Exercise Intervention in Individuals With Subacromial Impingement Syndrome: a Randomized, Controlled Clinical Trial Pilot Study

High Point University6 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2012年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
6
主要终点
Shoulder Pain and Disability Index Change over time

研究概览

简要总结

Specific Aims and Hypotheses Aims To investigate the incremental benefits of cervicothoracic spinal manipulation in addition to shoulder mobilization and exercise for improving range of motion, pain, physical function and fear avoidance beliefs in patients with subacromial shoulder impingement.

Hypotheses It is hypothesized that those subjects who receive spinal manipulation in addition to shoulder mobilization and exercise will achieve greater improvements in range of motion, pain, function and fear avoidance beliefs at two weeks following treatment conclusion, at 4 weeks following treatment conclusion, and at discharge when compared to the subjects who did not receive the spinal manipulation.

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)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • To be eligible, participants must meet the clinical prediction rule for unilateral subacromial shoulder impingement including: a) positive Hawkins-Kennedy impingement sign, b) positive painful arc sign, and c) weakness in external rotation with the arm at the side

排除标准

  • Individuals with contraindications to treatment with mobilization and manipulation (Appendix A) will be excluded

结局指标

主要结局

Shoulder Pain and Disability Index Change over time

时间窗: 2 weeks, 4 weeks, discharge

Patients will be followed for the duration of their physical therapy treatment. An average of 12 visits over 6 weeks

次要结局

  • Numeric Pain Rating Scale change over time(2 weeks, 4 weeks, discharge)
  • Fear Avoidance Beliefs Questionnaire change over time(2 weeks, 4 weeks, discharge)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

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