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

The purpose of this study is to evaluate the effectiveness of progressive strength training after rotator cuff and labrum operation of the shoulder joint.

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Key information

Conditions

Rotator Cuff Disease Shoulder Joint

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Jyväskylä Central Hospital

Jyväskylä, 40620, Finland

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Progressive exercise

Behavioral

home-based exercise program, 2 to 3 exercise sessions per week

Primary outcomes

Strength and mobility

Time frame: one year

Sponsors and collaborators

Lead sponsor

Jyväskylä Central Hospital

Other

Registry information

Official study title

Progressive Exercise After Operation of Rotator Cuff Rupture and Anterior Labrum Rupture: Randomized Controlled Trial

Important dates

Study start: 2006
Primary completion: 2009
Study completion: 2010
First posted: Feb 26, 2008
Registry last updated: May 27, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed