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Shoulder Training: Muscle Recruitment Patterns and the Effect of an Exercise Program
This study is currently recruiting participants.
Verified by University Ghent, April 2009
First Received: September 25, 2008   Last Updated: April 6, 2009   History of Changes
Sponsored by: University Ghent
Information provided by: University Ghent
ClinicalTrials.gov Identifier: NCT00774956
  Purpose

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


Condition Intervention
Shoulder Impingement
Procedure: Exercise training program

MedlinePlus related topics: Exercise and Physical Fitness
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: Shoulder Training: Muscle Recruitment Patterns and the Effect of an Exercise Program

Further study details as provided by University Ghent:

Primary Outcome Measures:
  • Muscle recruitment pattern [ Time Frame: After 6 weeks of training ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Shoulder pain and functional ability in the patient group [ Time Frame: After 6 weeks of training ] [ Designated as safety issue: No ]

Estimated Enrollment: 60
Study Start Date: September 2008
Estimated Study Completion Date: December 2010
Estimated Primary Completion Date: December 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental
Subject with shoulder impingement
Procedure: Exercise training program
A 6 week shoulder exercise training program
2: Active Comparator
Healthy persons
Procedure: Exercise training program
A 6 week shoulder exercise training program

  Eligibility

Ages Eligible for Study:   18 Years to 40 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

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
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00774956

Contacts
Contact: Kristof De Mey Kristof.demey@ugent.be

Locations
Belgium
University Ghent Recruiting
Ghent, Belgium, 9000
Principal Investigator: Guy Vanderstraeten, MD, PhD            
Principal Investigator: Ann Cools, PhD            
Sponsors and Collaborators
University Ghent
Investigators
Principal Investigator: Guy Vanderstraeten, MD, PhD University Ghent
Principal Investigator: Ann Cools, PhD University Ghent
  More Information

No publications provided

Responsible Party: University Ghent ( Ann Cools )
Study ID Numbers: 2008/432
Study First Received: September 25, 2008
Last Updated: April 6, 2009
ClinicalTrials.gov Identifier: NCT00774956     History of Changes
Health Authority: Belgium: Institutional Review Board

ClinicalTrials.gov processed this record on May 07, 2009