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

This study has been completed.
Sponsor:
Information provided by:
Jyväskylä Central Hospital
ClinicalTrials.gov Identifier:
NCT00624117
First received: February 15, 2008
Last updated: May 25, 2010
Last verified: May 2010
History of Changes
  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
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (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:

U.S. FDA Resources

Further study details as provided by Jyväskylä Central Hospital:

Primary Outcome Measures:
  • Strength and mobility [ Time Frame: one year ] [ Designated as safety issue: No ]

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

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
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
Please refer to this study by its ClinicalTrials.gov identifier: 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

No publications provided

Responsible Party: Jari Ylinen, MD, PhD, Jyväskylä Central Hospital
ClinicalTrials.gov Identifier: NCT00624117     History of Changes
Other Study ID Numbers: Dnro46/2005
Study First Received: February 15, 2008
Last Updated: May 25, 2010
Health Authority: Finland: Ethics Committee

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

Additional relevant MeSH terms:
Rupture
Wounds and Injuries

ClinicalTrials.gov processed this record on May 16, 2013