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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00998777
Other study ID # SwimmersShoulder
Secondary ID
Status Completed
Phase Phase 2
First received October 19, 2009
Last updated January 9, 2012
Start date September 2009
Est. completion date June 2010

Study information

Verified date January 2012
Source University of North Carolina, Chapel Hill
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The primary purpose of this study is to assess changes in shoulder muscle strength, shoulder movement, shoulder flexibility, muscle thickness, upper arm torsion angle, and subacromial width (space where the rotator cuff muscle passes through) after completing a 6-week shoulder strengthening and stretching program in division I collegiate swimmers. The result of this study may demonstrate the effectiveness of a strengthening and stretching program to positively influence factors that have been associated with pain and injury in division I collegiate swimmers and indicate the need to implement this program for the entire team. Following a 6-week strengthening and stretching program, it is believed that scapular kinematics, shoulder flexibility, and shoulder and scapular stabilizer strength will be improved compared to control subjects.


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date June 2010
Est. primary completion date June 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria:

- Subjects will be included in the study if they meet the following criteria:

- NCAA division I swimmers

- Participate in swimming for at least 30 minutes per day for 4 days per week.

- Participate in all team weight lifting sessions.

- Complete 15 of the 18 training sessions if the subject is placed in the treatment group.

Exclusion Criteria:

- Subjects will be excluded from the study if:

- They are currently being treated for shoulder pain

- They develop shoulder pain during the course of the intervention program

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Procedure:
Shoulder Strengthening
The intervention program is a 6 week shoulder and scapular stabilizer strengthening program that is performed 3 times per week. The program includes 10 exercises that are performed with Theraband rubber tubing and 2 stretches. The exercises are: shoulder flexion, Ys, Ts, Ws, IR @ 90, ER @ 90, Throwing acceleration, Throwing deceleration, dynamic hug, and low rows. The stretches include the sleeper stretch and the corner stretch.

Locations

Country Name City State
United States Dean E. Smith Center Chapel Hill North Carolina

Sponsors (1)

Lead Sponsor Collaborator
University of North Carolina, Chapel Hill

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Shoulder and Scapular Stabilizer Strength Measured pre and post test No
Secondary Scapular Kinematics Measured pre and post test No
Secondary Shoulder ROM Measured pre and post test No
Secondary Postural Assessment Measured pre and post test No
Secondary Width of subacromial space Measured pre and post test No
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