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

NCT04868006 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2022-09-08

No results posted yet for this study

Summary

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.

Conditions

  • Sports Physical Therapy

Interventions

PROCEDURE

End-range Maitland mobilization + proprioception training

End-range Maitland mobilization performed in end position of internal rotation of the shoulder accompanied with 8--week long proprioception training

PROCEDURE

Non end-range Maitland mobilization + proprioception training

Non end-range Maitland mobilization performed in loose position of the shoulder accompanied with 8--week long proprioception training

PROCEDURE

Sham manual therapy technique + proprioception training

Placebo performed in loose position of the shoulder accompanied with 8--week long proprioception training

Sponsors & Collaborators

  • University of Pecs

    lead OTHER

Principal Investigators

  • Miklós Pozsgai · Harkány Thermal Rehabilitation Centre

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
30 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-28
Primary Completion
2021-10-10
Completion
2021-10-10

Countries

  • Hungary

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04868006 on ClinicalTrials.gov