Opposite SI Joint Stretching for GIRD

January 29, 2018 updated by: Victor Romano, MD, Romano Orthopaedic Center

Sacroiliac Stretching Improves Glenohumeral Internal Rotational Deficit of the Opposite Shoulder in Baseball Players in a Randomized Control Study

The purpose of this study is to investigate if stretching the contralateral sacroiliac (SI) joint improves GIRD in baseball players. Additionally, we aimed to compare our SI joint stretching regiment with a classically described sleeper stretch routine.

Study Overview

Detailed Description

Abstract:

Background:

Glenohumeral Internal Rotational Deficit (GIRD) is a well-documented finding in throwing athletes.

Hypothesis/Purpose:

The purpose of this study is to investigate if stretching the contralateral sacroiliac (SI) joint improves GIRD in baseball players. Additionally, the effect of the SI joint stretch will be compared to that of the classically described sleeper stretch.

Study Design:

Randomized Controlled Clinical Trial

Methods:

With the athlete supine and arm abducted 90o, internal rotation of both shoulders was measured in 23 minor league baseball players.

Next, each player randomly was assigned to either a control (sleeper stretch of dominant shoulder) or experimental (stretch of the SI joint contralateral to the dominant shoulder) group supervised by a certified athletic trainer. The players performed their own stretches.

Finally, the initial two investigators, unaware of to which group the player was assigned, re-measured the end-range internal rotation of each athlete's dominant shoulder.

Study Type

Interventional

Enrollment (Actual)

23

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Illinois
      • Oak Park, Illinois, United States, 60302
        • Romano Orthopaedic Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

23 years to 25 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • All members a minor league baseball team

Exclusion Criteria:

  • Any active shoulder or back injury or history of shoulder or back injury

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Single Group Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Sleeper stretch group
A certified athletic trainer supervised and observed the athlete as he performed the sleeper stretch on his dominant shoulder.
Internal Range of motion of dominant shoulder
Experimental: Opposite SI joint Stretch
A certified athletic trainer supervised and observed the athlete as he performed the SI joint stretch opposite his dominant shoulder.
Internal range of motion of dominant shoulder

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Shoulder internal ROM after stretching opposite SI joint
Time Frame: Measurement made within 30 minutes of stretching
Internal range of motion of dominant shoulder after stretching opposite SI joint
Measurement made within 30 minutes of stretching

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Shoulder Internal ROM after sleeper stretch
Time Frame: Measurement made with 30 minutes of stretching
Internal range of motion of dominant shoulder after sleeper stretch
Measurement made with 30 minutes of stretching

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Victor Romano, Romano Orthopaedic Center

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 23, 2017

Primary Completion (Actual)

May 23, 2017

Study Completion (Actual)

May 23, 2017

Study Registration Dates

First Submitted

December 30, 2017

First Submitted That Met QC Criteria

January 29, 2018

First Posted (Actual)

February 5, 2018

Study Record Updates

Last Update Posted (Actual)

February 5, 2018

Last Update Submitted That Met QC Criteria

January 29, 2018

Last Verified

January 1, 2018

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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