Arm Pump in Motorcross Training

September 16, 2015 updated by: Prof. Dr. F. Staes, Universitaire Ziekenhuizen KU Leuven

Hand Strength Grip and Ergonomics of Driving as Risk Factors in the Etiology of Arm Pump in Motorcross Training

Arm Pump is a sport specific term drivers use to describe Acute or Chronic Compartment Syndrome of the forearm. Drivers experience pain in the forearms due to increased blood pressure in forearm muscle compartments. No strategies nor methods have been used to diminish the risk to suffer from arm pump within motor cross.

This project aims to look at ergonomics of driving and its relationship with the occurrence of arm pump.

The investigators will first investigate the experience of motor cross athletes with arm pump through motor cross federations in Belgium and The Netherlands (survey).

Two groups of athletes will be selected (20 persons within each group) who will be invited to the motor cross track to investigate their hand grip strength, motor driving position, muscle activity.

Study Overview

Status

Completed

Study Type

Observational

Enrollment (Actual)

11

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

    • Limbur
      • Lommel, Limbur, Belgium
        • Motor Cross Track

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

18 years to 50 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Recreational or competitive motor cycle athletes

Description

Inclusion Criteria:

  • recreational or competitive motor cycling athletes
  • with or without arm pump problems
  • signing informed consent
  • participation with their own motor bike
  • Regular training hours

Exclusion Criteria:

  • Inactive for more than 2 weeks before participation
  • Pathology at shoulder, elbow or wrist level (except for arm pump)

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

Cohorts and Interventions

Group / Cohort
persons without arm pump
persons with arm pump

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
motor ergonomics
Time Frame: March - June 2014 (3 months)
2D video-recording will be used to observe motor sitting position
March - June 2014 (3 months)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
hand grip strength
Time Frame: March - June 2014 (3 months)
Use of hand grip dynamometer (Biometrics) to measure hand grip strength.
March - June 2014 (3 months)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
muscle activity
Time Frame: March - June 2014 (3 months)
Use of surface electromyography in order to record muscle activity of forearm and upper arm musculature
March - June 2014 (3 months)

Collaborators and Investigators

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

April 1, 2014

Primary Completion (Actual)

December 1, 2014

Study Completion (Actual)

May 1, 2015

Study Registration Dates

First Submitted

March 21, 2014

First Submitted That Met QC Criteria

March 25, 2014

First Posted (Estimate)

March 26, 2014

Study Record Updates

Last Update Posted (Estimate)

September 17, 2015

Last Update Submitted That Met QC Criteria

September 16, 2015

Last Verified

September 1, 2015

More Information

Terms related to this study

Other Study ID Numbers

  • S56412

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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