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临床试验/NCT06739694
NCT06739694已完成不适用

The Efficacy of a Pain Neuroscience Education Programme in Shoulder Pain: a Randomised Clinical Trial

Universidad de León2 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2024年1月2日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
56
试验地点
2
主要终点
Pain

研究概览

简要总结

Objectives: The purpose of this study was to assess the efficacy of a pain neuroscience education programme applied to patients with shoulder pain.

详细描述

A randomised controlled trial was performed. Fifty-five patients satisfied eligibility criteria, agreed to participate, and were randomized into an experimental group (n = 27) or control group (n =28). A manual therapy and exercises program was administered for both groups. In addition, a pain neuroscience education protocol was administered for the experimental group for a whole period of 4 weeks (1 session/week, 75mins per session).

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 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Being 18-70 years of age.
  • History of shoulder pain of more than 3 months duration.
  • Presence of a painful arc
  • Medical diagnosis of shoulder pain with at least 2 positive impingement tests including Neer, Hawkins, or Jobe test

排除标准

  • Diagnosis of fibromyalgia.
  • Pregnancy.
  • A history of traumatic onset of shoulder pain.
  • Other histories of shoulder injury.
  • Torn tendons.
  • Ligamentous laxity based on a positive Sulcus and apprehension tests.
  • Numbness or tingling in the upper extremity.
  • Previous shoulder or cervical spine surgery.
  • Systemic illness.
  • Corticosteroid injection on the shoulder within 1 year of the study.
  • Physical therapy 6 months before the study.

结局指标

主要结局

Pain

时间窗: Baseline and 5 weeks.

Reduction in pain intensity using the Shoulder Pain and Disability Index (SPADI)

Disability

时间窗: Baseline and five weeks.

Improving functionality using the Shoulder Pain and Disability Index (SPADI)

次要结局

  • kinesiophobia(Baseline and 5 weeks.)

研究者

发起方
Universidad de León
申办方类型
Other
责任方
Principal Investigator
主要研究者

Eva Prado Robles

Principal Investigator and clinical Professor

Universidad de León

研究点 (2)

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