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

This study is currently recruiting participants.

Verified by Jyväskylä Central Hospital, August 2008

Sponsored by:	Jyväskylä Central Hospital
Information provided by:	Jyväskylä Central Hospital
ClinicalTrials.gov Identifier:	NCT00624117

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

MedlinePlus related topics: Exercise and Physical Fitness

U.S. FDA Resources

Study Type:	Interventional
Study Design:	Treatment, Randomized, Single Blind (Outcomes Assessor), Parallel Assignment, Efficacy Study
Official Title:	Progressive Exercise After Operation of Rotator Cuff Rupture and Anterior Labrum Rupture: Randomized Controlled Trial

Further study details as provided by Jyväskylä Central Hospital:

Primary Outcome Measures:

Strength and mobility [ Time Frame: one year ] [ Designated as safety issue: No ]

Estimated Enrollment:	100
Study Start Date:	May 2006
Estimated Study Completion Date:	December 2009
Estimated Primary Completion Date:	December 2008 (Final data collection date for primary outcome measure)

Arms	Assigned Interventions
A: Experimental	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

Contacts

Contact: Petri Salo, M.Sc

+358 14 2691092

petri.salo@ksshp.fi

Locations

Finland
Jyväskylä Central Hospital	Recruiting
Jyväskylä, Finland, 40620
Principal Investigator: Jari Ylinen, PhD

Sponsors and Collaborators

Jyväskylä Central Hospital

Investigators

Principal Investigator:

Jari Ylinen, PhD

Jyväskylä Central Hospital

More Information

Responsible Party:	Jyväskylä Central Hospital ( Jari Ylinen, MD, PhD )
Study ID Numbers:	Dnro46/2005
Study First Received:	February 15, 2008
Last Updated:	August 27, 2008
ClinicalTrials.gov Identifier:	NCT00624117
Health Authority:	Finland: Ethics Committee

Keywords provided by Jyväskylä Central Hospital:

shoulder joint
recovery of function
effectiveness of rehabilitation
rehabilitation

Study placed in the following topic categories:

Wounds and Injuries
Disorders of Environmental Origin
Rupture

ClinicalTrials.gov processed this record on January 16, 2009