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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00774956
Other study ID # 2008/432
Secondary ID
Status Completed
Phase N/A
First received September 25, 2008
Last updated March 19, 2012
Start date September 2008
Est. completion date June 2011

Study information

Verified date March 2012
Source University Ghent
Contact n/a
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the muscle recruitment pattern and the effect of a 6 week shoulder exercise training program in healthy persons and subjects with shoulder impingement


Recruitment information / eligibility

Status Completed
Enrollment 77
Est. completion date June 2011
Est. primary completion date June 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- current reported history of shoulder pain localised at the glenohumeral joint diagnosed as impingement

- two positive shoulder impingement tests

- pain reproduction during two of three additional categories of clinical tests

- the subject is able to perform pain-free arm elevations with a resistance of 0.5 kg

Exclusion Criteria:

- cervical and periscapular pain

- positive labral injury tests

- history of shoulder surgery

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Exercise training program
A 6 week shoulder exercise training program
Exercise training program
A 6 week shoulder exercise training program

Locations

Country Name City State
Belgium University Ghent Ghent

Sponsors (1)

Lead Sponsor Collaborator
University Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle recruitment pattern After 6 weeks of training No
Secondary Shoulder pain and functional ability in the patient group After 6 weeks of training No
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