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The Effect of A Rehabilitation Program on Patients with Multidirectional Instability of the Glenohumeral Joint: A Functional MRI Study

Not Applicable
Recruiting
Conditions
Multidirectional Instability (MDI) of at the Glenohumeral Joint
Physical Medicine / Rehabilitation - Physiotherapy
Musculoskeletal - Other muscular and skeletal disorders
Registration Number
ACTRN12621001207808
Lead Sponsor
Swinburne University of Technology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
60
Inclusion Criteria

Patients with MDI: Inclusion criteria
1. Symptomatic shoulder instability in at least 2 directions (one direction being inferior).
2. Aged 18 to 35 years
3. Female. MDI is more prevalent in the female population and excluding males will limit any bias due to potential gender effects.
4. Right shoulder affected. Participants with a right affected shoulder will be included in this study to limit the potential biases that may result from differences in measuring the left and right sides of the brain from participants with left and right shoulder problems. In this study, fMRI effects of the LEFT brain will be measured from participants with a right sided shoulder problem.
5. No history of trauma to the affected shoulder
6. No structural lesion on a clinical Magnetic Resonance Imaging scan.
7. Ability to understand the English language and willingness to participant in a rehabilitation program.

Aged Matched Control: Inclusion criteria
1. Aged and gender matched controls with no history of shoulder problems for each included MDI participant

Exclusion Criteria

Exclusion criteria for MDI and control groups:
•Male
•Shoulder instability due to trauma, central nervous system lesions, peripheral lesions and any other neurological disorders
•Patients with significant neck (cervical spine) pathology
•Participants will any history of shoulder surgery
•Inability to understand or speak English
•Existence of MRI contraindications
•Participants who are planning surgery between baseline and follow-up FMRI imaging
•Participants who are or are planning to become pregnant
•Patients with contraindications to standard MRI or fMRI

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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