Influence of Dental Occlusion on the Performance of High Level Rowers (IODPR) (IODPR)

Monocentric, prospective, randomized, open-label, cross-over study.

Study Overview

• Status: Terminated
• Conditions: Dental Occlusion, Traumatic
• Intervention / Treatment: Device: with artificial occlusal disturbance; Device: without artificial occlusal disturbance

Detailed Description

Current literature data suggest that dental occlusion has an influence on postural control in the general population, and more markedly in high-level athletes. The link between dental occlusion and the postural stability of top athletes has been studied in several disciplines such as basketball, shooting, golf and running. There is currently no data in the field of rowing. But this sport requires optimal postural control for synchronous and symmetrical muscle solicitation.

The present study aims to evaluate the influence of dental occlusion on postural stability and the performance of high level rowers.

Our assumptions are as follows:

• Occlusal disturbance alters the muscular power developed by high level rowers
• occlusal disturbance alters the static postural stability of high level rowers

• Study Type: Interventional
• Enrollment (Actual): 7
• Phase: Not Applicable

Contacts and Locations

Study Locations

• France
  • Hauts-de-France
    • Wattignies, Hauts-de-France, France, 59139
      • CREPS de Wattignies

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 15 years and older (ADULT, OLDER_ADULT, CHILD)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• High level rower, part of the Lille Rowing Hope Pole;
• At least 15 years old;
• Training at the Centre de Ressources, d'Expertise et de Performance Sportive (CREPS) de Wattignies during the period from 01/09/2017 to 31/10/2017;
• Having at least 28 natural or prosthetic teeth in occlusion;
• Not having consumed alcohol in the last 24 hours before the recordings;
• whose parents have given free, informed and written consent for minors;
• Having given free and informed consent, in writing supplemented by the consent of at least one holder of parental authority, if he is a minor;
• Affiliated, himself or through his parents if he is a minor, to a social security scheme.

Exclusion Criteria:

• Current antecedent(s) or pathology(s) likely to disturb the balance: neurological, ear nose and throat, ophthalmological, orthopedic;
• Temporomandibular joint disorder (s) (pain and / or noise);
• Orofacial symptoms (headache, tinnitus, facial myalgia, bruxism);
• Dental and / or periodontal care in progress;
• Chronic pain requiring daily use of analgesics for more than three months;
• Pregnant or lactating woman;
• Concurrent participation in another study;
• Major persons subject to legal protection (safeguard of justice, guardianship, tutorship) and persons deprived of their liberty.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: BASIC_SCIENCE
• Allocation: RANDOMIZED
• Interventional Model: SEQUENTIAL
• Masking: NONE

Number of Arms

1

Arms and Interventions

Participant Group / Arm

Intervention / Treatment

OTHER: Rowing training session; Power tests, balance and tonicity tests are performed eyes opened and eyes closed : with artificial occlusal disturbance and; without artificial occlusal disturbance

Device: with artificial occlusal disturbance; A silicon artificial occlusal disturbance is made from a mould of the rowers mouth and placed in the mouth during the training session. With artificial occlusal disturbance : Maximal Intercuspal Occlusion (MIO) with silicone splint increases the vertical dimension of occlusion of 1, 2 and 4 mm.; Device: without artificial occlusal disturbance; The training session is performed without occlusal disturbance

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Muscular power	Muscular power (in Watts) developed by the high level rowers with the "leg press" test on a "Dyno concept 2" machine, with and without artificial occlusal disturbance. Each test lasts 30 seconds. The sequence consists in 2 tests and is performed twice with a resting period of 1 min between each recording.	At the time of inclusion

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Surface of the pressure center of the rower's feet	Each test lasts 51.2 seconds. The sequence consists in 10 tests and is performed twice with a resting period of 1 min between each recording. During each test, the projected sway area (in mm², the area of the confidence ellipse containing 90% of the sampled positions of the foot pressure center on the statokinesigram) is extracted from the stabilometric platform	At the time of inclusion
Velocity of the pressure center of the rower's feet	Each test lasts 51.2 seconds. The sequence consists in 10 tests and is performed twice with a resting period of 1 min between each recording. During each test, the sway velocity (in mm/s) is calculated as the speed of displacement of the center of pressure of the foot as a function of the average position on the antero-posterior axis of the statokinesigram.	At the time of inclusion
Tonicity of the para-vertebral muscles	Tonicity of the para-vertebral muscles is evaluated with the postural test of Posterior-superior iliac spines (PSIS) with and without artificial occlusal disturbance. This PSIS test is performed eyes opened, in MIO position with and without artificial occlusal disturbance, The sequence of two tests is performed twice. During this test, the endpoint is qualitative: operator asymmetric thumbs' ascension reflecting asymmetric contraction of paravertebral muscles (abnormal response) or not (normal response).	At the time of inclusion

Collaborators and Investigators

• Sponsor: Rennes University Hospital
• Investigators: Principal Investigator: Xavier MD RAVALEC, Rennes University Hospital

Study record dates

Study Major Dates

• Study Start (ACTUAL): October 27, 2017
• Primary Completion (ACTUAL): November 22, 2017
• Study Completion (ACTUAL): November 22, 2017

Study Registration Dates

• First Submitted: May 25, 2018
• First Submitted That Met QC Criteria: August 23, 2018
• First Posted (ACTUAL): August 27, 2018

Study Record Updates

• Last Update Posted (ACTUAL): August 27, 2018
• Last Update Submitted That Met QC Criteria: August 23, 2018
• Last Verified: August 1, 2018

More Information

Terms related to this study

• Keywords: young elite rowers
• Additional Relevant MeSH Terms: Stomatognathic Diseases; Tooth Diseases; Malocclusion; Dental Occlusion, Traumatic; Anti-Infective Agents; Dermatologic Agents; Antifungal Agents; Keratolytic Agents; Salicylic Acid
• Other Study ID Numbers: 35RC17_8823_IODPR

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No