Manual Therapy Versus Conventional Rehabilitation Protocol on Subacromial Pain Syndrome

Not Applicable

Completed

• Conditions: Subacromial Impingement Syndrome
• Interventions: Other: accelerated protocol and mulligan method

• Registration Number: NCT04057170
• Lead Sponsor: Cukurova University

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2018-03-01
• Primary Completion: 2018-10-01
• Study Completion: 2018-11-30
• Status Verified: 2019-08
• Study First Submitted: 2019-08-13
• Study First Submitted QC: 2019-08-13
• Last Update Submitted: 2019-08-13
• Study First Posted: 2019-08-15
• Last Update Posted: 2019-08-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 42

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
mulligan method	accelerated protocol and mulligan method	Mulligan mobilization with mowement method every three days for six weeks
accelerated protocol	accelerated protocol and mulligan method	accelerated rehabilitation protocol every three days for six weeks

Primary Outcome Measures

Name	Time	Method
Subacromial Interval Measurement	six weeks	Subacromial interval measurement was performed via anterior-posterior shoulder radiography
Shoulder Pain and Disability Index	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	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	two weeks	Conventional goniometer with 1° increments is used to determine shoulder limitations due to pain in patients

Trial Locations

Locations (1)

Volkan Deniz; 🇹🇷 Ankara, Turkey