Core Stability Measures as a Risk Factor for the Development of Lower Extremity Injuries in Physical Education Students

November 10, 2017 updated by: University Ghent

Core Stability as a Risk Factor for the Development of Lower Extremity Injuries: a Prospective Study

Male and female physical education students were subjected to a clinical test battery comprised of valid and reliable tests to measure different aspects of core stability at the start of the study. After a period of 2 months testing, the injury registration procedure started with the use of an online injury registration platform and regular call back moments. After 2 years of injury registration, all data was gathered and will be analysed statistically to link the measured core stability aspects as risk factors for certain lower extremity injuries.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

September 2014 - December 2014: 139 male and female participants 18+ were subjected to different test to evaluate corresponding aspects of core stability. The following test were performed: Star excursion balance test; Lumbopelvic proprioception test; Lumbopelvic neuromuscular control test; Lateral step down test; Hip strength test measured with a handheld dynamometer(flexion/extension/abduction/adduction/internal rotation/external rotation); Trunk strength tests measured with a handheld dynamometer (trunk flexion and trunk extension) and core muscle endurance tests (prone bridging test/Biering-Sorenson test/side bridging tests).

January 2015 - April 2017: Prospective follow up of lower extremity injury contracted during sports activity. The injuries were confirmed by a medical examiner and were recorded in an online injury registry platform (Survey Monkey).

Statistical analysis will be performed to evaluate which core stability outcome measure can be considered a risk factor for the development of lower extremity injuries.

Study Type

Interventional

Enrollment (Actual)

139

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

      • Ghent, Belgium, 9000
        • Vakgroep REVAKI (Ghent University - Ghent University Hospital)

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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

- 1st year of physical education study (enrolled at the Artevelde graduate school or the Ghent graduate school

Exclusion Criteria:

  • Musculoskeletal injury at the time of study participation
  • Pre-existing lower back injury
  • Pre-existing lower extremity injury (less than 6 months prior to study participation)

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

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Healthy cohort
Core stability test
A test battery comprised of field tests to evaluate core stability

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Core muscle strength
Time Frame: 2 hours
Isometric strength of trunk flexor and trunk extensor musculature measured in Newton
2 hours
Hip strength
Time Frame: 2 hours
Isometric strength of hip flexor, hip extensor, hip abductor, hip adductor and hip rotator muscles measured in Newton
2 hours
Postural control
Time Frame: 2 hours
Anterior, posterolateral and posteromedial reaching distance during unipodal stance, measured in cm
2 hours
Core muscle endurance
Time Frame: 2 hours
Endurance capacity of ventral, dorsal and lateral core musculature, measured in seconds
2 hours
Sensorimotor control of core musculature
Time Frame: 2 hours
Propriocention and neuromuscular control of the lumbopelvic muscles using a qualitative assessment sheet
2 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Injury history
Time Frame: 2 hours
Previous lower extremity injuries, recorded using a questionnaire
2 hours

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Philip Roosen, PT, PhD, University Ghent

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)

September 1, 2014

Primary Completion (Actual)

December 31, 2015

Study Completion (Actual)

April 1, 2017

Study Registration Dates

First Submitted

November 10, 2017

First Submitted That Met QC Criteria

November 10, 2017

First Posted (Actual)

November 17, 2017

Study Record Updates

Last Update Posted (Actual)

November 17, 2017

Last Update Submitted That Met QC Criteria

November 10, 2017

Last Verified

November 1, 2017

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

No individual participant data will be shared after completion of the study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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.

Clinical Trials on Leg Injuries

Clinical Trials on Core stability tests

Subscribe