Clinical Trials Directory

Trials / Completed

CompletedNCT03425357

Sonoelastography of the Supraspinatus Tendon

Responsiveness of Sonoelastography in the Supraspinatus Tendon

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
23 (actual)
Sponsor
Karen Brage · Academic / Other
Sex
All
Age
40 Years – 60 Years
Healthy volunteers
Not accepted

Summary

This study aims a determine the responsiveness of sonoelastography in the tendinopathy-affected supraspinatus tendon.

Detailed description

The trial will include 20 patients diagnosed with supraspinatus tendinopathy from one orthopaedic shoulder clinic in Denmark. The intervention will consist of an exercise program including lowload exercises with elastics and dumbbells, targeting the rotator cuff in a 12 weeks home-exercise program with two control visits at a physiotherapy department at the hospitals. Tissue elasticity (measured by sonoelastography) is used as the primary outcome and is measured 12 weeks post baseline

Conditions

Interventions

TypeNameDescription
OTHERLow Load ExercisesAll rotator cuff and scapular exercises are performed with 3 sets of 20 repetitions 3 times per week for 12 weeks. The load is set at around 60% of 1 RM (20 reps). The glenohumeral/postural corrective exercises are performed with 3 sets of 5 repetitions (The position is held for 15 seconds per repetition).

Timeline

Start date
2018-03-25
Primary completion
2019-08-15
Completion
2019-08-21
First posted
2018-02-07
Last updated
2019-08-22

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT03425357. Inclusion in this directory is not an endorsement.