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Progressive Exercise After Operation of Rotator Cuff Rupture and Anterior Labrum Rupture

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00624117
First Posted: February 26, 2008
Last Update Posted: May 27, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Jyväskylä Central Hospital
  Purpose
The purpose of this study is to evaluate the effectiveness of progressive strength training after rotator cuff and labrum operation of the shoulder joint.

Condition Intervention
Rotator Cuff Disease Shoulder Joint Behavioral: Progressive exercise

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Progressive Exercise After Operation of Rotator Cuff Rupture and Anterior Labrum Rupture: Randomized Controlled Trial

Resource links provided by NLM:


Further study details as provided by Jyväskylä Central Hospital:

Primary Outcome Measures:
  • Strength and mobility [ Time Frame: one year ]

Enrollment: 100
Study Start Date: May 2006
Study Completion Date: February 2010
Primary Completion Date: February 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: A Behavioral: Progressive exercise
home-based exercise program, 2 to 3 exercise sessions per week

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • rupture of rotator cuff
  • rupture of anterior labrum
  • age 18 to 65 years
  • motivated to continue in work life
  • motivated for rehabilitation

Exclusion Criteria:

  • former operation in the same joint
  • major arthrosis in the same joint
  • cervical disk herniation
  • concised spinal cord
  • conditions after cervical spine operations
  • rheumatic diseases
  • fibromyalgia
  • pregnancy
  • severe depression
  • alcoholism
  • misusing of drugs
  • disease that prevents progressive exercise eg. back pain, heart disease
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00624117


Locations
Finland
Jyväskylä Central Hospital
Jyväskylä, Finland, 40620
Sponsors and Collaborators
Jyväskylä Central Hospital
Investigators
Principal Investigator: Jari Ylinen, PhD Jyväskylä Central Hospital
  More Information

Responsible Party: Jari Ylinen, MD, PhD, Jyväskylä Central Hospital
ClinicalTrials.gov Identifier: NCT00624117     History of Changes
Other Study ID Numbers: Dnro46/2005
First Submitted: February 15, 2008
First Posted: February 26, 2008
Last Update Posted: May 27, 2010
Last Verified: May 2010

Keywords provided by Jyväskylä Central Hospital:
shoulder joint
recovery of function
effectiveness of rehabilitation
rehabilitation

Additional relevant MeSH terms:
Rupture
Wounds and Injuries