Mobilization and Mobilization With Movement Effect on Sub Acromial Space in Impingement Syndrome.

October 1, 2020 updated by: Riphah International University

Effect of Shoulder Mobilization and Mobilization With Movement on Sub Acromial Space in Shoulder Impingement.

Mobilization and mobilization with movement both treatment techniques are effective in impingement syndrome.The objective of our study is to compare the effects of shoulder mobilization and mobilization with movement on subacromial space in impingement syndrome.

Study Overview

Status

Completed

Detailed Description

A study was conducted in 2016 to determine the effect of MWM in Impingement syndrome on sub acromial space, pain and disability. In this study,15 patients diagnosed with sub acromial impingement were selected and treated for six sessions. MWM posterolateral glide was the intervention selected. The results showed the p value of <0.00001 for pre and post treatment sessions of MWM in patients with Impingement syndrome. According to the results it was concluded that in terms of decreasing the pain and disability as well as increasing the acromiohumeral distance MWM is effective treatment for impingement syndrome.

An RCT was conducted in 2016 to find out the effect of posterolateral glide MWM on pain, strength of shoulder muscles and upward rotation of scapula. 31 patients were allocated to a group performing exercises actively and other group who received posterolateral glides MWM. The results suggested that MWM was effective intervention in decreasing pain on VAS and improving strength of external rotators.

A study was conducted in 2013 to compare the effects of supervised exercise with and without manual therapy for impingement syndrome.The results showed marked differences in reducing pain and increasing ROM and strength of rotator muscles in group that received supervised exercise with manual therapy. So it was concluded that manual therapy with exercise program is effective in decreasing pain and improving ROM than exercises alone in impingement syndrome.

A study was conducted to compare the effects of mobilization with movement and mobilization with therapeutic exercises in patients of subacromial impingement. The results are suggestive that shoulder mobilization and MWM with exercises result in more reduction of pain and improved AROM.

A RCT was conducted to compare the effectiveness of joint and soft tissue mobilization techniques and self-training program. The results of this study showed that patient who received manual therapy showed significant differences. So it was concluded that joint mobilization is effective intervention for patients with impingement syndrome.

Studies have been conducted in the past on effect of mobilization and mobilization with movement on shoulder impingement but they did not report their effect on sub acromial space in impingement syndrome using musculoskeletal ultrasound and the comparison of both techniques.

The purpose of this study is to find out the effects of mobilization and mobilization with movement on sub acromial space using musculoskeletal ultrasound in impingement syndrome and compare their outcomes.

Study Type

Interventional

Enrollment (Actual)

22

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Fedral
      • Islamabad, Fedral, Pakistan, 46000
        • Max Rehab & Physical Therapy Centre G-8 Markaz

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

30 years to 50 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Impingement Syndrome Screening using Neer Impingement Test, Hawkin Kennedy Test.
  • Patients with impingement syndrome in acute phase.

Exclusion Criteria:

  • Frozen Shoulder
  • Thoracic Outlet Syndrome
  • Cervical Radiculopathy
  • Any Fracture or dislocation of shoulder girdle.
  • Diabetic Patients.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Mobilization
Mobilization, heat application, ultrasound, TENS

Moist hot pack for 10 mins/1 set/ 6 consecutive days, Ultrasound for 5 mins/1 set/ 6 consecutive days, TENS on shoulder region for 10 mins/1 set/ 6 consecutive days, Shoulder mobilization posterolateral glide for 30 secs with 30 secs rest for 5 mins.

A total of 6 consecutive sessions were given each consisting of 30 mins.

Active Comparator: Mobilization with movement
Mobilization with movement, heat application, ultrasound, TENS

Moist hot pack for 10 mins/1 set/ 6 consecutive days, Ultrasound for 5 mins/1 set/ 6 consecutive days, TENS on shoulder region for 10 mins/1 set/ 6 consecutive days, Shoulder mobilization with movement (MWM) 10 repetitions with 30 secs rest for 5 mins.

A total of 6 consecutive sessions were given each consisting of 30 mins.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Sub acromial Space
Time Frame: 6th day
Changes from baseline, for measuring sub acromial space, patients were seated with arm resting at the side with fully extended elbow, trunk in neutral position and ultrasound images were taken using linear transducer probe. The ultrasound transducer was positioned on the shoulder over the acromion and humeral head. AHD was measured using onscreen calipers by finding superior aspect of head of humerus and inferior aspect of acromion (between apex of greater tubercle of humerus and inferior edge of acromial process). Three readings were taken which then averaged for a single reading.
6th day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Supraspinatus Tendon Thickness
Time Frame: 6th day
Changes from baseline, Transducer was placed on shoulder over subacromial space with the notch diagonally facing down towards the belly button, measured in transverse view lateral to the biceps tendon of long head.
6th day
Numeric Pain Rating Scale
Time Frame: 6th day
Changes from baseline, Numeric pain rating scale is a scale from 0 to 10. 0 indicating no pain and 10 indicating worse pain.
6th day
Range of motion ( ROM)
Time Frame: 6th day
Changes from baseline, shoulder ROM were taken using goniometer
6th day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Asghar Khan, PhD, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 6, 2019

Primary Completion (Actual)

September 10, 2020

Study Completion (Actual)

September 13, 2020

Study Registration Dates

First Submitted

October 1, 2020

First Submitted That Met QC Criteria

October 1, 2020

First Posted (Actual)

October 8, 2020

Study Record Updates

Last Update Posted (Actual)

October 8, 2020

Last Update Submitted That Met QC Criteria

October 1, 2020

Last Verified

October 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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