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Dynamic Posturographic Testing and Motor Learning Predictability in Gymnasts

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ClinicalTrials.gov Identifier: NCT00374569
Recruitment Status : Completed
First Posted : September 11, 2006
Last Update Posted : January 27, 2016
Information provided by (Responsible Party):

Study Description
Brief Summary:
One aim of this study was to find if there was a difference between balance and stability between elite level gymnasts and non-gymnasts. Another aim was to find if there was a relationship between dynamic posturographic scores associated with sway fatigue or adaptability and the ability to learn new gymnastic routines. The ultimate aim of the study was to improve gymnastic performance while reducing the probability of injury.

Condition or disease Intervention/treatment Phase
Gymnastics Injury, Motor Learning, Balance Procedure: Gymnastic Routine Early Phase 1

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Detailed Description:
Computerized dynamic posturography outcomes will be obtained on elite level gymnasts and non gymnasts who will be age matched. The outcome measurement will be obtained using computerized dynamic posturography, a standard diagnostic test of balance function (41-46). The subject's balance was tested using a three-component force platform (CAPS test) under one sensory condition of the modified Clinical Test of Sensory Interaction on Balance (mCTSIB), the eyes closed on perturbing surface condition. This condition was chosen as studies have shown it to be the single test that best correlates with balance impairment and falls. The stability score, already used in several studies by other authors will be used as the primary outcome measure in this research. It is defined as 1 minus the ratio between the measured sway during the test (computed as the major axis of a standard 95% confidence ellipse) and the amount of sway a normal subject of the same height as the one being tested should be able to sway before falling (also known as the theoretical maximum sway or the theoretical limit of stability, calculated using a regression formula based on the subject's height developed by NASA in 1962 and commonly used in all posturographic tests). For convenience, the stability score will be expressed as a percentage. Its definition makes it a convenient and easy to understand measure to use as a subject able to stand perfectly still with no sway will have a score of 100%, whereas one that sways as much as the limit of stability will have a score of 0%. During each test, the subject's sway will be determined by the force platform and its related software. The CAPS three-component force platform uses 3 load cells arranged in a triangle to measure the distribution of the vertical ground reaction force on the platform. The analog load cell signals are amplified and simultaneously sampled by the platform electronics using three synchronized individual 24bit delta-sigma analog to digital converters sampling at 312kHz and decimating the samples to a data rate of 64Hz. The use of three A/D converters insures that the signals from the 3 load cells are acquired simultaneously with no timing error. The high sampling rate with the high decimation and low data rate of the sigma-delta converters eliminates aliasing and provides a resolution of about 4 parts per million. The digital load cell data was then sent via a USB connection to the PC where software uses a calibration matrix determined by the manufacturer to compute the total vertical force and the two horizontal moments acting on the platform. From these data, the software computed the point of application of the vertical force acting on the platform, commonly referred to as the Center of Pressure (CoP). The location of the CoP coincides in static conditions with the projection of the subject's Center of Mass (CoM) onto the platform, and its movement relates to the movements of the subject's CoM (sway). The determination of the actual sway will require the determination of the instantaneous location of the CoM via the location and inertial properties of each body segment of the specific subject being tested. The CAPS test, like all posturographic equipment, uses the movement of the CoP as an approximation of the sway. Because it is an approximation, and because for kinetic reasons the CoP moves more than the CoM, the 95% confidence interval of the CoP motion was considered. This will allow the CAPS software to compute the ellipse that represents the location of all of the sway samples collected during the test with 95% confidence. The major axis of this ellipse will represent the maximum sway of the subject in any direction during the test and it will be used to compute the stability score. To assess the accuracy and resolution of the measurement chain, calibrated weights of 75kg and 100kg will be positioned in the center of the force platform (as if it were a subject) and 20s acquisitions will be performed: the accuracy of the weight must be within the instrument's factory specifications (+-2N). Therefore the accuracy for the position claimed by the manufacturer of +-1mm for a weight of 75kg will be accepted as correct as it determination will require specialized equipment and software available only to the manufacturer. It should be noted that the overall accuracy of the position of the CoP given by the instrument will not be relevant in this study as the motion of the CoP determined the sway. The sway measurement error will be estimated considering the fact that during the test at both weights the dead weight must not move, but the measurement chain will indicate a "sway" of less then 0.05mm (measurement noise), therefore the resolution of the measurement chain and the sway measurement error will be considered to be 0.05mm. To verify the repeatability of the measurement chain, the same type of tests will be repeated two times, obtaining similar results (within the specified accuracy and resolution). Given the sway measurement error, the measurement error in the stability score will be determined. From the definition of the stability score it is clear that the least the theoretical limit of stability, the more pronounced the effect of the sway measurement error is. As the theoretical limit of stability is computed by using the formula 0.55*height*2*sin(6.25°), the shorter the subject, the more the stability score is sensitive to the measurement errors. To estimate the stability score measurement error a subject's height of 1.6m will be considered. Such a subject will have a theoretical limit of stability of 191.6mm. For such a subject, a sway measurement error of 0.05mm means a stability score measurement error of 0.05/191.6 or, if the score is expressed in percentage, of 0.026%. Thus, any changes in the stability score greater than that will be a consequence of the subject's sway and not of measurement errors. A CAPS dynamic posturography test in the eyes closed perturbed stance will be obtained on all subjects. Subjects will be instructed that they will stand on a foam platform and close their eyes while data will be obtained from a computerized force plate. The subjects will be given practice sessions so that they will be familiar with the test prior to the collection of data. The CAPS test occurs over 25 seconds. We will divide the degree of sway observed during the first half of the test and the second half of the test and will obtain ratios. Subjects whose sway will increase in the second half of the test in reference to the first half will be identified as demonstrating a fatigability ratio. Individuals who will demonstrate less sway in the second half of the test will be identified as demonstrating an adaptability ratio that we consider might be related to some type of motor learning. All gymnasts will be instructed in a novel gymnastic routine which will include a variety of inverted postures and ground routines unfamiliar to the subjects. The athletes will be allowed to practice the routine for one hour after which they will be asked to perform the routine in front of the same judge who will be blinded as to the outcome measures previously obtained. The performance scores will be then compared to the CDP measurements to ascertain if there would be any relationship.

Study Design

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 300 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Dynamic Posturographic Testing and Motor Learning Predictability in Gymnasts
Study Start Date : June 2005
Primary Completion Date : July 2006
Study Completion Date : September 2006
Arms and Interventions

Arm Intervention/treatment
Experimental: Gymnastics
Gymnasts stand on a computerized dynamic posturography Force Plate and Stability is measured and gymnastic routines performed
Procedure: Gymnastic Routine
A combination of gymnastic movements are performed
Experimental: Non Gymnasts
Non Gymnasts stand on a computerized dynamic posturography Force Plate and Stability is measured and gymnastic routines performed
Procedure: Gymnastic Routine
A combination of gymnastic movements are performed

Outcome Measures

Primary Outcome Measures :
  1. Dynamic Posturography [ Time Frame: pre and post ]
    stability testing pre and post gymnastic routines

Secondary Outcome Measures :
  1. Blinded expert judging of motor performance in Gymnastics [ Time Frame: pre and post immediate ]
    Judging of gymnastic performance

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   10 Years to 30 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Elite level Gymnasts
  • Non Gymasts control

Exclusion Criteria:

  • Non Elite level Gymnasts
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00374569

United States, Texas
Carrick Institute for Graduate Studies Texas
Dallas, Texas, United States, 75267
Sponsors and Collaborators
Carrick Institute for Graduate Studies
Study Chair: Frederick R Carrick, PhD, FACCN Carrick Institute for Graduate Studies
Principal Investigator: Guido Pagnacco, PhD Carrick Institute for Graduate Studies
Principal Investigator: Elena Oggero, PhD Carrick Institute for Graduate Studies
Study Chair: Brandon Brock, DC Carrick Institute for Graduate Studies
Principal Investigator: Tina Arikan, DC Carrick Institute for Graduate Studies
More Information

Responsible Party: Frederick Carrick, PhD, FACCN, Principal Investigator, Carrick Institute for Graduate Studies
ClinicalTrials.gov Identifier: NCT00374569     History of Changes
Other Study ID Numbers: CI-05-05
First Posted: September 11, 2006    Key Record Dates
Last Update Posted: January 27, 2016
Last Verified: January 2016
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Keywords provided by Frederick Carrick, PhD, FACCN, Carrick Institute for Graduate Studies:
Gymnastics, Computerized Dynamic Posturography, Balance