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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01749553
Other study ID # Pro00011276
Secondary ID GO18000461
Status Completed
Phase N/A
First received
Last updated
Start date October 2011
Est. completion date February 2012

Study information

Verified date September 2021
Source University of Alberta
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To Determine whether an eight-week posterior shoulder stretch was effective in increasing dominant arm internal rotation(IR) and horizontal adduction (HAd) range of motion (ROM) in a group of overhead athletes identified as having tightness of their posterior shoulder structures.


Recruitment information / eligibility

Status Completed
Enrollment 37
Est. completion date February 2012
Est. primary completion date February 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria: - varsity level athletes involved in volleyball, tennis and swimming with internal rotation deficit of greater than or equal to 15 degrees Exclusion Criteria: - previous surgical procedure or fracture of either shoulder or presently receiving treatment for condition affecting either shoulder

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Sleeper Stretch
Posterior shoulder stretch technique

Locations

Country Name City State
Canada Department of Physical Therapy, Universiy of Alberta Edmonton Alberta

Sponsors (1)

Lead Sponsor Collaborator
University of Alberta

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Shoulder internal rotation and horizontal adduction range of motion 8 weeks
Secondary Rate of change in internal rotation and horizontal adduction range of motion 0 - 4 weeks and 4 - 8 weeks