Manual Therapy Versus Conventional Rehabilitation Protocol on Subacromial Pain Syndrome

Subacromial Impingement Syndrome Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04057170
• Other study ID #: 0
• Status: Completed
• Phase: N/A
• Start date: March 1, 2018
• Est. completion date: November 30, 2018

Study information

• Verified date: August 2019
• Source: Cukurova University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 42
• Est. completion date: November 30, 2018
• Est. primary completion date: October 1, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

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

Related Conditions & MeSH terms

• Shoulder Impingement Syndrome
• Shoulder Pain
• Subacromial Impingement Syndrome
• Syndrome

Intervention

Other:
• accelerated protocol and mulligan method
manual therapy technic

Locations

Country	Name	City	State
Turkey	Volkan Deniz	Ankara

Sponsors (1)

Lead Sponsor	Collaborator
Cukurova University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Shoulder Pain and Disability Index	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	two weeks
Primary	Visual Analogue Scale	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	two weeks
Primary	Active Range of Motion measurement	Conventional goniometer with 1° increments is used to determine shoulder limitations due to pain in patients	two weeks
Primary	Subacromial Interval Measurement	Subacromial interval measurement was performed via anterior-posterior shoulder radiography	six weeks