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NCT00624117 Clinical Trial

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

Rotator Cuff Disease Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00624117
Other study ID # Dnro46/2005
Secondary ID
Status Completed
Phase N/A
First received February 15, 2008
Last updated May 25, 2010
Start date May 2006
Est. completion date February 2010

Study information
Verified date May 2010
Source Jyväskylä Central Hospital
Contact n/a
Is FDA regulated No
Health authority Finland: Ethics Committee
Study type Interventional

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date February 2010
Est. primary completion date February 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility 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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• Progressive exercise
home-based exercise program, 2 to 3 exercise sessions per week

Locations
Country Name City State
Finland Jyväskylä Central Hospital Jyväskylä

Sponsors (1)
Lead Sponsor Collaborator
Jyväskylä Central Hospital

Country where clinical trial is conducted

Finland, 

Outcome
Type Measure Description Time frame Safety issue
Primary Strength and mobility one year No
See also
  Status Clinical Trial Phase
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Completed NCT00925366 - Which is the Most Reliable Radiologic Examination for the Diagnosis of Rotator Cuff Tendon Tear? N/A
Not yet recruiting NCT01069224 - Analysis of Proinflammatory Factors in the Synovial Fluid In Patients With Rotator Cuff Disease N/A
Completed NCT00640575 - Subacromial Ultrasound-guided or Systemic Steroid Injection for Rotator Cuff Disease, a Randomized Double Blinded Study N/A
Recruiting NCT04805242 - Effects of Dextrose Prolotherapy in Rotator Cuff Disease N/A
Completed NCT02474342 - Autologous Adipose Tissue Derived Mesenchymal Stem Cells for Rotator Cuff Disease N/A
Completed NCT03205852 - Patients Decision-making in Rotator Cuff Surgery N/A
Completed NCT02025400 - Internet Enhanced, Patient-Centered Orthopedic Care: A Prospective, Randomized, Controlled Pilot Trial Phase 1
Completed NCT00845715 - Early Range of Motion Following Arthroscopic Rotator Cuff Repair N/A
Completed NCT00500630 - Objective Evaluation of Shoulder Pathology and Surgery N/A