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临床试验/NCT04057170
NCT04057170已完成不适用

Comparison of the Effects of Mulligan Mobilization With Movement Method and Accelerated Rehabilitation Protocol on Shoulder Pain and Functions in Subacromial Pain Syndrome: A Randomized Single Blind Trial

Cukurova University2 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2018年3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
入组人数
42
试验地点
2
主要终点
Subacromial Interval Measurement

研究概览

简要总结

This study compares the periodic effects of Accelerated rehabilitation protocol (ARP) and Mulligan mobilization with mowement method (MWM) in subacromial pain syndrome patients rehabilitation. Half of the participants will receive ARP, while the other half will receive MWM.

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 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • to be in the 18-60 age range, to be cooperative during evaluation and treatment and to accept to participate in the study

排除标准

  • the presence of adhesive capsulitis, surgical indication or shoulder surgery, cervicothoracic problems (such as stenosis and disc herniation) diagnosed as neurological or inflammatory joint diseases

研究组 & 干预措施

mulligan method

Experimental

Mulligan mobilization with mowement method every three days for six weeks

干预措施: accelerated protocol and mulligan method (Other)

accelerated protocol

Experimental

accelerated rehabilitation protocol every three days for six weeks

干预措施: accelerated protocol and mulligan method (Other)

结局指标

主要结局

Subacromial Interval Measurement

时间窗: six weeks

Subacromial interval measurement was performed via anterior-posterior shoulder radiography

Shoulder Pain and Disability Index

时间窗: two weeks

It consists of 13 questions in two sections as 5 pain questions and 8 disability questions. Both sections are scored with VAS. The total score range is between 0-130 and it is calculated with the percentage score. Pain and disability are inversely proportional with the percentage score

Visual Analogue Scale

时间窗: two weeks

to record pain intensity during rest and active shoulder movements. The patient is asked to mark the point corresponding to the pain (0 no pain and 10 maximal pain) on 10 cm horizontal line. The distance between the marked point and the beginning is recorded as a pain score

Active Range of Motion measurement

时间窗: two weeks

Conventional goniometer with 1° increments is used to determine shoulder limitations due to pain in patients

次要结局

未报告次要终点

研究者

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

Volkan Deniz, PT

Director, Clinical Research

Cukurova University

研究点 (2)

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