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肩胛骨 Blackburn 稳定与 PNF 在撞击综合征中的比较 (impingment)

2026年9月30日 更新者:Mostafa Esmat Fouad Ebrahem、Cairo University

肩胛骨布莱克本稳定与本体感觉神经肌肉促进在肩峰下撞击综合征中的比较

purpose of study to Aim to investigate effect(s) of scapular Blackburn stabilization exercises compared toscapular proprioceptive neuromuscular facilitation (SPNF) exercise in addition to conventional exercises on shoulder pain, function, shoulder,sacpular ROM, scapular muscle strength and scapular orientation in patients with sub acromial impingement syndrome

Participants will be randomly allocated to three groups as follow:

Group A (n=17): will receive a program of conventional exercise include rotator cuff strengthening ,stretching for posterior capsule and stretching for pectoralis minor for 18 sessions (3 sessions per week for six weeks) Group B (n=17): will receive a scapular PNF exercise program in addition to conventional Exercise with the same frequency. Group C (n=17): will receive a scapular Blackburn stabilization exercises in addition to conventional Exercise with the same frequency

研究概览

详细说明

Sub-acromial impingement syndrome(SIS) is the most frequent cause of pain and overhead reach limitation in the shoulder area. It occurs when there is impingement of tendons or bursa in the shoulder from bones of the shoulder. Intrinsic and extrinsic factors that contribute to the development of SIS include inflammation in the supra humeral space, inhibition of the rotator cuff muscles, degeneration of the rotator cuff tendons, abnormal scapular position and kinematics. Currently SIS covers a range of pathologies from sub acromial bursitis to rotator cuff tendinopathy and full thickness rotator cuff tears.

The trial will guide physical therapists in selecting effective therapeutic interventions for patients with SAIS and scapular dyskinesia, aiming to reduce the number of treatment sessions, speed up recovery, and improve shoulder pain and functional abilities.

Scapular Blackburn stabilization exercise minimizes excessive superior translation of the humeral head in the glenoid fossa during elevation and subacromial space impingement, consequently addressing shoulder impingement. It also strengthens the scapulothoracic and rotator cuff muscles and decreases muscle imbalance.

Proprioceptive Neuromuscular Facilitation has been described as a comprehensive rehabilitation concept, promoting motor learning, motor control, strength and mobility.

This comprehensive rehabilitation approach includes task-oriented training with manual facilitation aimed at motor learning and motor control.

therefore, what are the effects of scapular Blackburn stabilization and PNF techniques in addition to conventional exercises on shoulder pain, function, shoulder ROM, scapular muscle strength, and scapular orientation in patients with sub acromial impingement syndrome?

研究类型

介入性

注册 (实际的)

51

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Giza Governorate
      • Cairo、Giza Governorate、埃及、022
        • faculty of physical therapy Cairo university

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

30年 至 50年 (成人)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • 1. Fifty one Male and female patients with SIS and aged between 30-50.

    2. Body mass index (BMI) 18.5-29.9 kg/m2.

    3. patients complaining primary shoulder impingement.

    4. patients with altered scapular resting positions with scapular dyskinesia with positive lateral scapular slide test.

    5- patients will be included at least three special tests positive from the following tests:

A-Hawkins-Kennedy Impingement Test:

B-Neer"s Impingement Test:

C- "Empty Can" or Jobe Test D-painful arc test

E-External rotation resistance test

F-Cross-body adduction test

G-Drop arm sign

Exclusion Criteria:

  • 1- Neurological deficit affecting the shoulder function during daily activities.

    2-Cervical disc pathology.

    3- Brain injures.

    4- Fractures in the upper limb

    5-Undergone shoulder surgery

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:Experimental.

receive a scapular PNF exercise program in addition to conventional Exercise ,

scapular Blackburn stabilization

实验性的:Experimental

receive a scapular Blackburn stabilization exercises in addition to conventional Exercise

PNF plus Exercise

其他:control group

Exercise only

Exercise only

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
shoulder pain and functional disability
大体时间:Assessment procedure will be performed pre intervention and post third and sixth week of treatment

Shoulder pain and disability index., minimum number 0=mean No pain and No disabilities and maximum number 10=mean highest pain and maximum disability

Assessment procedure will be performed pre intervention and post third and sixth week of treatment
A-shoulder flexion ROM B- shoulder external rotation C-shoulder internal rotation
大体时间:Assessment procedure will be performed pre intervention and post third and sixth week of treatment

Digital Inclinometer.

Assessment procedure will be performed pre intervention and post third and sixth week of treatment
selective muscle strength on: A- upper trapezius B- middle trapezius C-lower trapezius. D- serrates anterior
大体时间:Assessment procedure will be performed pre intervention and post third and sixth week of treatment

-Lafayette Hand-held dynamometer

Assessment procedure will be performed pre intervention and post third and sixth week of treatment
scapula orientation
大体时间:Assessment procedure will be performed pre intervention and post third and sixth week of treatment

lateral scapular slide test

Assessment procedure will be performed pre intervention and post third and sixth week of treatment

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Enas F. Youssef, Prof.Dr、chair person of Department of Physical therapy for Musculoskeletal Disorder and its Surgery

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2024年7月30日

初级完成 (实际的)

2025年6月30日

研究完成 (实际的)

2025年7月30日

研究注册日期

首次提交

2024年7月18日

首先提交符合 QC 标准的

2024年8月13日

首次发布 (实际的)

2024年8月15日

研究记录更新

最后更新发布 (实际的)

2026年10月5日

上次提交的符合 QC 标准的更新

2026年9月30日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • Blackburn versus PNF

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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