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Glenohumeral Internal Rotation Deficit (GIRD)

U

University Ghent

Status

Completed

Conditions

Glenohumeral Internal Rotation Deficit (GIRD)

Treatments

Procedure: home stretching program

Study type

Interventional

Funder types

Other

Identifiers

NCT01422083
2010/372

Details and patient eligibility

About

A loss of mobility in the shoulder in direction of internal rotation is associated with shoulder tendon pathology. Cause-effect relationship between these two is still not clear. It is suspected that this loss of mobility reduces the size of the tunnel in which this shoulder tendon is lying, namely the subacromial space. Overhead athletes frequently show glenohumeral internal rotation deficit (GIRD) while being healthy and free of shoulder pain. This makes this population interesting to investigate. This study wants to look at shoulders of overhead athletes with GIRD and measure the size of the subacromial space. After this, the athletes will be instructed to perform a home stretching program and at the end the effect of this on mobility and the size of the subacromial space will be measured.60 athletes will be recruited and randomly allocated to the control group and the stretching group. Before they start stretching, subacromial space size will be measured by use of ultrasound. This is a safe and non-invasive measuring tool. Mobility will be measured by use of a digital inclinometer. This also is safe and non-invasive. Patients will be instructed a stretching exercise, which they will be performing at home once a day during 6 weeks. At the end all outcome measures will be reassessed.

Enrollment

30 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • overhead athletes: at least 3 hours/week training
  • male and female
  • 18-30 years of age
  • No shoulder pain during last 3 months for which a doctor was consulted
  • No shoulder surgery
  • No neck diseases

Exclusion criteria

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

Control group
No Intervention group
Description:
This group of athletes do not perform a 6-week stretching program.
Home stretching program
Experimental group
Description:
These athletes take on a home stretching program (sleeper's stretch).
Treatment:
Procedure: home stretching program

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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