Effect of an Exercise Program of the Scapular Muscle Stabilizers in Amateur Kayakers Shoulder Pain

July 3, 2015 updated by: CEU San Pablo University
The purpose of this study is to determine whether a specific strengthening program for the stabilizing scapular muscle can reduce shoulder pain of amateur kayaker.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

11

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

  • Spain
    • Madrid
      • Boadilla del Monte, Madrid, Spain, 28668
        • San Pablo CEU University

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

12 years to 28 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • There Have Been practicing kayaking over 3 years.
  • There Have Been shoulder pain during sports at least 1 month of evolution

Exclusion Criteria:

  • Shoulder pain was caused by a traumatic injury.
  • To be in medical, pharmacological or shoulder physiotherapy treatment during the study.
  • To have been surgically intervened in the shoulder

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: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Exercise program
Procedure: Exercise program of the scapular muscle stabilizers

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Change in pain level during kayakergometer test
Time Frame: participants will be followed for the duration of kayakergometer test, an expected average of 30 minutes
participants will be followed for the duration of kayakergometer test, an expected average of 30 minutes

Secondary Outcome Measures

Outcome Measure
Time Frame
change in the time of appearance of the symptoms during kayakergometer test.
Time Frame: participants will be followed for the duration of kayakergometer test, an expected average of 30 minutes
participants will be followed for the duration of kayakergometer test, an expected average of 30 minutes

Collaborators and Investigators

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

Sponsor

CEU San Pablo University

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

May 1, 2014

Primary Completion (Actual)

September 1, 2014

Study Completion (Actual)

October 1, 2014

Study Registration Dates

First Submitted

July 18, 2014

First Submitted That Met QC Criteria

July 18, 2014

First Posted (Estimate)

July 21, 2014

Study Record Updates

Last Update Posted (Estimate)

July 7, 2015

Last Update Submitted That Met QC Criteria

July 3, 2015

Last Verified

July 1, 2014

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CEU-008

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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