Shoulder Injury Prevention Program in Swimmers

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00998777
Recruitment Status : Completed
First Posted : October 20, 2009
Last Update Posted : January 11, 2012
Information provided by (Responsible Party):
University of North Carolina, Chapel Hill

October 19, 2009
October 20, 2009
January 11, 2012
September 2009
June 2010   (Final data collection date for primary outcome measure)
Shoulder and Scapular Stabilizer Strength [ Time Frame: Measured pre and post test ]
Same as current
Complete list of historical versions of study NCT00998777 on Archive Site
  • Scapular Kinematics [ Time Frame: Measured pre and post test ]
  • Shoulder ROM [ Time Frame: Measured pre and post test ]
  • Postural Assessment [ Time Frame: Measured pre and post test ]
  • Width of subacromial space [ Time Frame: Measured pre and post test ]
Same as current
Not Provided
Not Provided
Shoulder Injury Prevention Program in Swimmers
The Effect of a 6-week Shoulder Strengthening Program on Scapular Kinematics and Shoulder Strength in Division I Collegiate Swimmers
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.
Not Provided
Phase 2
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Prevention
Shoulder Injury
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.
Other Name: Shoulder injury prevention, tubing program for athletes
Experimental: Shoulder Strengthening
The shoulder strengthening program is a 6-week intervention aimed to improve shoulder and scapular stabilizer strength and scapular kinematics. The program includes 10 exercises: shoulder flexion, Ys,Ts,Ws, Throwing Acceleration, Throwing Deceleration, Low Rows, Dynamic Hug, IR @ 90, and ER @ 90. The program also includes 2 stretches: sleeper stretch and corner stretch.
Intervention: Procedure: Shoulder Strengthening
Not Provided

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
Same as current
June 2010
June 2010   (Final data collection date for primary outcome measure)

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
Sexes Eligible for Study: All
18 Years to 25 Years   (Adult)
Contact information is only displayed when the study is recruiting subjects
United States
Not Provided
Not Provided
University of North Carolina, Chapel Hill
University of North Carolina, Chapel Hill
Not Provided
Principal Investigator: Elizabeth Hibberd UNC-Chapel Hill
Study Director: Joseph B Myers, PhD, ATC UNC- Chapel Hill
University of North Carolina, Chapel Hill
January 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP