Glenohumeral Internal Rotation Deficit in Non-pitcher Overhead Athletic Athletes: Case Series Analysis of Athletes (GIRDAhtlFMUI)

September 6, 2020 updated by: Andri Maruli Tua Lubis, Indonesia University

In this observational case series the investigators would like to investigate wether or not the strenuous activity exerted on over head athletic athletes (ie. javelin throwers, discus throwers) may incite injury on their shoulders.

The investigators understood that these athletes had to perform repeated throwing motions and yet reports on their effects are very limited. This condition in the long run may contribute to injury and affecting performance of the athletes.

The investigators found that these relationships have not been looked at closely by others and largely overshadowed by athletes in other fields; such injury patterns had been described in details in baseball pitchers but not in other athletes.

Study Overview

Detailed Description

Description of protocol:

In this study, the investigators would recruit athletes from the national athletics federation training in our city.

Data collection:

History taking:

  • complaints of shoulder stiffness
  • need for prolonged warm-up
  • pain
  • discomfort relating to the shoulders

Physical examination:

  • Bilateral shoulder range of motion (internal and external rotation)
  • Posterior shoulder flexibility test (denotes internal rotation deficit)
  • Scapular malpositioning, inferior medial border prominence, coracoid pain and malposition and dyskinesis of scapular movement (SICK) scapula rating

Notes: measurements are taken by at least two investigators separately and compared to ensure accuracy.

Results are presented in a table and analysed.

Study Type

Observational

Enrollment (Anticipated)

10

Contacts and Locations

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

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

National athletic athletes that performed overhead throwing motion in their sports that meet the inclusion criteria within our city.

Description

Inclusion Criteria:

  • Performed overhead throwing motions in their athletic skills
  • Athletes have competed in regional and national level
  • Undergoing active training

Exclusion Criteria:

  • Apparent anatomical deformity
  • Sustaining injury(ies)

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

  • Observational Models: Ecologic or Community
  • Time Perspectives: Cross-Sectional

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Glenohumeral internal rotation deficit
Time Frame: 1 day
A deficit of >20 degrees between dominant and non-dominant shoulder
1 day

Collaborators and Investigators

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

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 (Anticipated)

September 1, 2020

Primary Completion (Anticipated)

October 1, 2020

Study Completion (Anticipated)

October 1, 2020

Study Registration Dates

First Submitted

May 31, 2020

First Submitted That Met QC Criteria

June 4, 2020

First Posted (Actual)

June 5, 2020

Study Record Updates

Last Update Posted (Actual)

September 9, 2020

Last Update Submitted That Met QC Criteria

September 6, 2020

Last Verified

September 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • GIRD-Ahtl-FMUI

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

IPD Plan Description

There is a plan to make IPD and related data dictionaries available.

IPD Sharing Time Frame

The IPD will become available starting 6 months after publication.

IPD Sharing Access Criteria

The information will be shared electronically via email to other researchers after review by the principal investigator.

IPD Sharing Supporting Information Type

  • Study Protocol

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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