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Clinical Trials/NCT04057170
NCT04057170
Completed
Not Applicable

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 University1 site in 1 country42 target enrollmentMarch 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Subacromial Impingement Syndrome
Sponsor
Cukurova University
Enrollment
42
Locations
1
Primary Endpoint
Subacromial Interval Measurement
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
March 1, 2018
End Date
November 30, 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Volkan Deniz, PT

Director, Clinical Research

Cukurova University

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

  • 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

Outcomes

Primary Outcomes

Subacromial Interval Measurement

Time Frame: six weeks

Subacromial interval measurement was performed via anterior-posterior shoulder radiography

Shoulder Pain and Disability Index

Time Frame: 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

Time Frame: 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

Time Frame: two weeks

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

Study Sites (1)

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