Effect Study of an Eccentric Training Program and Stretching for Patients With Chronical Rotator Cuff Tendinopathy

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00782522

Enrollment

Registered

2008-10-31

Start date

2009-04-30

Completion date

2012-02-29

Last updated

2012-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronical Rotator Cuff Tendinopathy

Brief summary

In the first part of the the study two new outcome measurements (force reproducibility and subacromial space) will be tested for reproducibility. Therefore 30 healthy people will be assessed. In a second part of the study 60 patients will be randomly allocated to two groups. Group A (n=30) will perform a traditional training program and group B (n=30) will perform an eccentric training program. Before the onset of the training programs, pain, function, maximal force, range of motion, subacromial space and force reproducibility will be assessed. Both training programs will be accomplished at home. The first six weeks there will be an appointment with the therapist once a week to explain, correct and when necessary, aggravate the exercises. The next six weeks these appointments will be diminished to once every two weeks. After 6 and after 12 weeks of training the patients will be reassessed for all the parameters.

Interventions

PROCEDUREEccentric training program

Eccentric training program

PROCEDURETraditional training program

Traditional training program

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 75 Years

Healthy volunteers

Yes

Inclusion criteria

* global tendon thinning * inhomogeneous echo partitioning * calcifications at the insertion * symptoms present for at least 3 months: painful resisted isometric abduction, painful palpation of the supraspinatus tendon, impingement tests positive

Exclusion criteria

* documented full thickness rotator cuff rupture * other lesions than CRCT at the moment of the study * echographic criteria for ruptures (focal thinning, fluid-filled gap,compressibility)

Design outcomes

Primary

Measure	Time frame
Maximum force, pain and function,range of motion, force reproduction, subacromial space	After 6 and after 12 weeks of training

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026