Back to resultsManual Therapy Versus Conventional Rehabilitation Protocol on Subacromial Pain Syndrome
Primary Purpose
Subacromial Impingement Syndrome
Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
accelerated protocol and mulligan method
Sponsored by
About this trial
This is an interventional treatment trial for Subacromial Impingement Syndrome focused on measuring shoulder pain
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
Sites / Locations
- Volkan Deniz
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
mulligan method
accelerated protocol
Arm Description
Mulligan mobilization with mowement method every three days for six weeks
accelerated rehabilitation protocol every three days for six weeks
Outcomes
Primary Outcome Measures
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
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
Active Range of Motion measurement
Conventional goniometer with 1° increments is used to determine shoulder limitations due to pain in patients
Subacromial Interval Measurement
Subacromial interval measurement was performed via anterior-posterior shoulder radiography
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04057170
Brief Title
Manual Therapy Versus Conventional Rehabilitation Protocol on Subacromial Pain Syndrome
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
Study Type
Interventional
2. Study Status
Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
March 1, 2018 (Actual)
Primary Completion Date
October 1, 2018 (Actual)
Study Completion Date
November 30, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cukurova University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Subacromial Impingement Syndrome
Keywords
shoulder pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
42 (Actual)
8. Arms, Groups, and Interventions
Arm Title
mulligan method
Arm Type
Experimental
Arm Description
Mulligan mobilization with mowement method every three days for six weeks
Arm Title
accelerated protocol
Arm Type
Experimental
Arm Description
accelerated rehabilitation protocol every three days for six weeks
Intervention Type
Other
Intervention Name(s)
accelerated protocol and mulligan method
Intervention Description
manual therapy technic
Primary Outcome Measure Information:
Title
Shoulder Pain and Disability Index
Description
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
Time Frame
two weeks
Title
Visual Analogue Scale
Description
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
Time Frame
two weeks
Title
Active Range of Motion measurement
Description
Conventional goniometer with 1° increments is used to determine shoulder limitations due to pain in patients
Time Frame
two weeks
Title
Subacromial Interval Measurement
Description
Subacromial interval measurement was performed via anterior-posterior shoulder radiography
Time Frame
six weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
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
Facility Information:
Facility Name
Volkan Deniz
City
Ankara
ZIP/Postal Code
06560
Country
Turkey
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Manual Therapy Versus Conventional Rehabilitation Protocol on Subacromial Pain Syndrome
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