End-range Maitland Mobilization on Glenohumeral Internal Rotation Deficit and Proprioception

September 4, 2022 updated by: University of Pecs

The Effect of End-range Maitland Mobilization on Glenohumeral Internal Rotation Deficit and Proprioception in Volleyball Players

Glenohumeral internal rotation deficit (GIRD) is one of the main reasons for glenohumeral pain in athletes with over-head activity. As GIRD increases, the ratio between internal and external rotation changes resulting in decreased joint stability.

Joint mobilization is a possible option for the decrease of GIRD and contribution to improvement of proprioception in addition to physical therapy. The aim of this trial is to investigate the effect of end-range Maitland mobilization in addition to physical therapy on GIRD, other joint movements and proprioception.

Study Overview

Detailed Description

Glenohumeral internal rotation deficit (GIRD) is one of the main reasons for glenohumeral pain in athletes with over-head activity. As GIRD increases, the ratio between internal and external rotation changes resulting in decreased joint stability. The occurence of GIRD and decreased joint proprioception may lead to different shoulder pathologies (e.g. Impingement syndrome).

Joint mobilization is a possible option for the decrease of GIRD and contribution to improvement of proprioception in addition to physical therapy. Several joint mobilization techniques exists, which can be applied for stretching of periarticular tissues. Maitland mobilization is a well applied mobilization type. The effectiveness of both end-range and not end-range Maitland mobilization in lengthening of periarticular tissues and improvement of joint proprioception has been previously confirmed amongst several diseases. However, the effect of end-range Maitland mobilization on decrease of GIRD and proprioception in addition to physical therapy has not been investigated in volleyball players so far.

The aim of this trial is to investigate the effect of end-range Maitland mobilization in addition to physical therapy on GIRD, other joint movements and proprioception.

Study Type

Interventional

Enrollment (Actual)

60

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

    • Please Select
      • Harkány, Please Select, Hungary, 7815
        • Harkány Thermal Rehabilitation Centre

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

18 years to 30 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • National Championship players in I. or II. level
  • at least, 10 degree deficit of glenohumeral internal rotation in the dominant shoulder compared to the non-dominant hand

Exclusion Criteria:

  • previous trauma or surgery on the dominant shoulder
  • participation in any kind of treatment during the intervention period

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: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: End-range mobilization + proprioception training
End-range Maitland mobilization performed in end-range internal rotation of the shoulder accompanied with 8--week long proprioception training
End-range Maitland mobilization performed in end position of internal rotation of the shoulder accompanied with 8--week long proprioception training
Active Comparator: Non end-range mobilization+ proprioception training
Non end-range Maitland mobilization performed in loose position of the shoulder accompanied with 8--week long proprioception training
Non end-range Maitland mobilization performed in loose position of the shoulder accompanied with 8--week long proprioception training
Sham Comparator: Sham manual therapy technique + proprioception training
Placebo performed in loose position of the shoulder accompanied with 8--week long proprioception training
Placebo performed in loose position of the shoulder accompanied with 8--week long proprioception training

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Internal rotation of the dominant glenohumeral joint
Time Frame: after 8 weeks
Measurement of active internal rotation of the dominant glenohumeral joint with goniometer expressed in degree
after 8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Flexion of the dominant glenohumeral joint
Time Frame: after 8 weeks
Measurement of active flexion of the dominant glenohumeral joint with goniometer expressed in degree
after 8 weeks
Extension of the dominant glenohumeral joint
Time Frame: after 8 weeks
Measurement of active extension of the dominant glenohumeral joint with goniometer expressed in degree
after 8 weeks
Abduction of the dominant glenohumeral joint
Time Frame: after 8 weeks
Measurement of active abduction of the dominant glenohumeral joint with goniometer expressed in degree
after 8 weeks
Adduction of the dominant glenohumeral joint
Time Frame: after 8 weeks
Measurement of active adduction of the dominant glenohumeral joint with goniometer expressed in degree
after 8 weeks
External rotation of the dominant glenohumeral joint
Time Frame: after 8 weeks
Measurement of active external rotation of the dominant glenohumeral joint with goniometer expressed in degree
after 8 weeks
Western Ontario Shoulder Instability Index
Time Frame: after 8 weeks
Western Ontario Shoulder Instability Index of the dominant shoulder
after 8 weeks
Posterior Shoulder Endurance Test
Time Frame: after 8 weeks
Muscle strength test of the dominant shoulder expressed in Newton
after 8 weeks
Proprioception of the shoulder
Time Frame: after 8 weeks
Proprioception of the shoulder measured with plurimeter expressed in degree
after 8 weeks
Davies test
Time Frame: after 8 weeks
Measurement of proprioception and muscle strength test by the Davies test expressed in amount of success touch
after 8 weeks
Sportspecific proprioception test
Time Frame: after 8 weeks
Measurement of the precision of serving expressed in centimeter
after 8 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Miklós Pozsgai, Harkány Thermal Rehabilitation Centre

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.

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)

September 28, 2021

Primary Completion (Actual)

October 10, 2021

Study Completion (Actual)

October 10, 2021

Study Registration Dates

First Submitted

April 22, 2021

First Submitted That Met QC Criteria

April 27, 2021

First Posted (Actual)

April 30, 2021

Study Record Updates

Last Update Posted (Actual)

September 8, 2022

Last Update Submitted That Met QC Criteria

September 4, 2022

Last Verified

September 1, 2022

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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