跳至主要内容
临床试验/NCT03568006
NCT03568006已完成不适用

Effectiveness of Passive Mobilization of Glenohumeral Joint in Patients With Subacromial Syndrome: a Randomized Controlled Trial

Universidad San Jorge2 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2018年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
22
试验地点
2
主要终点
Visual Analogue Scale (VAS)

研究概览

简要总结

From a biomechanical point of view, subacromial syndrome causes an increment in the anterior and superior translation of the humeral head, which increases compression in the adjacent tissues of the subacromial space, aggravating the symptoms of the patients. Conservative treatments are the first option for subacromial syndrome management, despite the fact that there is limited evidence about its effectiveness, due to the lack of experimental studies.

The aim of this study is to evaluate the effectiveness of a passive joint mobilization (caudal and dorsal gliding) grade II in the glenohumeral joint, within a multimodal approach to reduce pain and improve the range of motion in patients with subacromial syndrome.

详细描述

Subacromial syndrome, also known as subacromial impingement, is the most frequent disorder in the shoulder joint. It has a multifactorial origin and represents a wide spectrum of pathologies. Its main consequences are pain and loss of function in the glenohumeral joint. From a biomechanical point of view, subacromial syndrome causes an increment in the anterior and superior translation of the humeral head, which increases compression in the adjacent tissues of the subacromial space, aggravating the symptoms of the patients. Conservative treatments are the first option for subacromial syndrome management, despite the fact that there is limited evidence about its effectiveness, due to the lack of experimental studies.

The aim of this study is to evaluate the effectiveness of a passive joint mobilization (caudal and dorsal gliding) grade II in the glenohumeral joint, within a multimodal approach to reduce pain and improve the range of motion in patients with subacromial syndrome. To this end, a randomized clinical trial will be carried out in the Montpellier Clinic in Zaragoza. Twenty-two patients will be recruited and randomly assigned to one of the two groups (intervention and control). Both groups will receive a standardized treatment consisting of: 10 sessions of infrared rays, and a program of therapeutic exercises and indications to improve their postural hygiene. In addition, the intervention group will receive a passive joint mobilization in the glenohumeral joint of 5 minutes. Pain intensity, range of motion and functionality of the glenohumeral joint will be measured in the first session before any treatment and in the tenth session after the treatment.

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
Double (Investigator, Outcomes Assessor)

盲法说明

It is not possible to mask physiotherapists and patients, so the only masking will be for researchers and evaluators

入排标准

年龄范围
30 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of subacromial syndrome
  • Pain at rest, which increases when doing active movements
  • Neer´s impingement test positive
  • Hawkins Kennedy test positive
  • Pain lasting more than one month
  • Anteriorization of humeral head
  • Full capacity (physical and cognitive) to participate in the study and give consent.

排除标准

  • Infiltrations during the previous six months
  • Traumatic origin of pain
  • Complete tear of any rotator cuff tendon
  • Bilateral pain
  • Previous surgical intervention in the affected shoulder
  • Patients planning to start with other treatments during the clinical trial.

研究组 & 干预措施

Intervention

Experimental

Intervention will consist of passive joint mobilization (caudal and dorsal gliding) grade II in the glenohumeral joint.

Besides, participants will receive a standardized treatment consisting of infrared rays, a program of therapeutic exercises and indications to improve their postural hygiene.

干预措施: Specific passive mobilization (Other)

Intervention

Experimental

Intervention will consist of passive joint mobilization (caudal and dorsal gliding) grade II in the glenohumeral joint.

Besides, participants will receive a standardized treatment consisting of infrared rays, a program of therapeutic exercises and indications to improve their postural hygiene.

干预措施: Standardized treatment (standard protocol) (Other)

Control

Active Comparator

Control treatment will consist of a standardized treatment consisting of infrared rays, a program of therapeutic exercises and indications to improve their postural hygiene.

干预措施: Standardized treatment (standard protocol) (Other)

结局指标

主要结局

Visual Analogue Scale (VAS)

时间窗: Change between baseline (immediately before intervention) and post intervention (2 weeks).

10 centimetres Visual Analogue Scale. 0 is no pain, whilst 10 is maximum intolerable pain

次要结局

  • Active range of motion(Change between baseline (immediately before intervention) and post intervention (2 weeks).)
  • Constant Score(Change between baseline (immediately before intervention) and post intervention (2 weeks).)

研究者

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

Pablo Herrero Gallego

Dr. Pablo Herrero, PT, PhD. Head of iPhysio Research Group.

Universidad San Jorge

研究点 (2)

Loading locations...

相似试验