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Sponsors and Collaborators: |
University Ghent BOF |
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Information provided by: | University Ghent |
ClinicalTrials.gov Identifier: | NCT00782522 |
In the first part of the the study two new outcome measurements (force reproducibility and tendon stiffness) will be tested for reproducibility.
Therefore 30 healthy people will be assessed. In a second part of the study 60 patients will be randomly allocated to two groups. Group A (n=30) will perform a traditional training program and group B (n=30) will perform an eccentric training program. Before the onset of the training programs, pain, function, maximal force, range of motion, tendon stiffness and force reproducibility will be assessed.
Both training programs will be accomplished at home. The first four weeks there will be an appointment with the therapist once a week to explain, correct and when necessary, aggravate the exercises. The next eight weeks these appointments will be diminished to once every two weeks.
After the 12 weeks of training the patients will be reassessed for all the parameters.
For detection of long term effects of the eccentric training program, the patients will be assessed a third time at three months after the end of the training program.
Condition | Intervention |
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Chronical Rotator Cuff Tendinopathy |
Procedure: Eccentric training program Procedure: Traditional training program |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study |
Official Title: | Effect Study of an Eccentric Training Program and Stretching for Patients With Chronical Rotator Cuff Tendinopathy |
Estimated Enrollment: | 90 |
Study Start Date: | April 2009 |
Estimated Study Completion Date: | December 2010 |
Estimated Primary Completion Date: | December 2010 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
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1: Experimental
Eccentric training program
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Procedure: Eccentric training program
Eccentric training program
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2: Active Comparator
Traditional training program
|
Procedure: Traditional training program
Traditional training program
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Ages Eligible for Study: | 20 Years to 50 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
Contact: Annelies Maenhout | Annelies.maenhout@ugent.be |
Belgium | |
University Hospital Ghent | Recruiting |
Ghent, Belgium, 9000 | |
Principal Investigator: Lieven De Wilde, MD, PhD |
Principal Investigator: | Ann Cools, PhD | University Ghent |
Responsible Party: | University Ghent ( Ann Cools ) |
Study ID Numbers: | 2008/380 |
Study First Received: | October 29, 2008 |
Last Updated: | April 6, 2009 |
ClinicalTrials.gov Identifier: | NCT00782522 History of Changes |
Health Authority: | Belgium: Institutional Review Board |
Tendinopathy Tendon Injuries Muscular Diseases |
Musculoskeletal Diseases Wounds and Injuries Disorders of Environmental Origin |
Tendinopathy Tendon Injuries Muscular Diseases |
Musculoskeletal Diseases Wounds and Injuries Disorders of Environmental Origin |