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Clinical Trials/NCT01423682
NCT01423682CompletedNot Applicable

The Influence of Eccentric Training on the Volume and Vascularisation of the Rotator Cuff in Patients With Rotator Cuff Tendinopathy and Healthy Subjects

University Ghent1 site in 1 country60 target enrollmentStarted: April 1, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
60
Locations
1
Primary Endpoint
Tendon vascularisation examination.

Study Overview

Brief Summary

Patients with rotator cuff tendinopathy make up a large part of the population in physiotherapy practice. The rotator cuff, a shoulder muscle group, plays an important role in causing pain. Tendons suffer large compression and friction, which can lead to degeneration of these tendons. Rehabilitation often leads to unsatisfying results.

In Achilles and patella tendinopathy, a new training program called eccentric training has shown very good results. Eccentric training contains exercises during which a force has to be resisted while the muscle lengthens instead of shortens. This would have a larger influence on tendon tissue. Some small studies also show promising results of eccentric training in patients with rotator cuff tendinopathy but the mechanisms behind these results remain unclear.

To investigate this, 30 patients with rotator cuff tendinopathy and 30 healthy subjects will be evaluated before and immediately after performing the exercise. Three measurements will be done: ultrasonographic measurement of tendon thickness, power Doppler imaging and measurement of microcirculation around the tendon with Oxygen to see. All measurements are non-invasive, pain free and without risks for the human body.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Male/ Female
  • •18-40 years old
  • •Unilateral shoulder pain for at least 3 months
  • •Pain of at least 3/10 on a visual analogue scale
  • •Painful arc or pain at end range abduction
  • •2/3 impingement tests positive
  • •2/4 resistance tests positive
  • •Pain at insertion rotator cuff

Exclusion Criteria

  • •Spurling test positive
  • •Shoulder surgery in the past
  • •Osteoarthritis shoulder
  • •Full thickness ruptures
  • •Inclusion Criteria Healthy subjects:
  • •Male/ Female
  • •18-40 years old
  • •Exclusion Criteria Healthy subjects:
  • •Shoulder pain during the last 3 months
  • •Shoulder surgery in the past
  • •Neck pain or disability
  • •Systemic disease (e.g. Marfan, Ehlers Danlos,...)

Arms & Interventions

Healthy subjects

Placebo Comparator

Intervention: Eccentric exercise (Behavioral)

Rotator cuff tendinopathy

Active Comparator

Intervention: Eccentric exercise (Behavioral)

Outcomes

Primary Outcomes

Tendon vascularisation examination.

Time Frame: After 30 minutes rest, before performing the exercise.

Power Doppler ultrasound examination is used.

Tendon thickness measurement

Time Frame: After 30 minutes rest, before performing the exercise.

Grey scale ultrasound examination is used.

Microcirculation around the tendon examination.

Time Frame: After 30 minutes rest, before performing the exercise.

Oxygen to see (spectrophotometry and laser Doppler) will be used.

Secondary Outcomes

  • Tendon thickness measurements.(10 minutes after performing the exercise.)
  • Tendon vascularisation examination.(10 minutes after performing the exercise.)
  • Microcirculation around the tendon examination.(10 minutes after performing the exercise.)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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