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Enrolling by invitation NCT07556211

Neuromuscular Function and Performance in Athletes With or Without Bruxism

Observational Bruxism

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Bruxism. Basic parameters: 18 years — 35 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Belgium
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Is Bruxism Associated With Altered Systemic Neuromuscular Function and Increased Risk of Muscular Injury ?

Overview

The aim of this study is to evaluate the associations between bruxism and neuromuscular function, as well as athletic performance, in a population of amateur athletes. Particular attention will be paid to musculoskeletal disorders associated with bruxism, particularly in the shoulder. Participants' history of sports injuries will also be recorded. To control for the effect of potential confounding variables, levels of stress, anxiety, and mood, as well as sleep quality, will be systematically measured using validated questionnaires.

Primary outcome measures

  • Muscular Tone [Time frame: Baseline]
  • Dynamic Stiffness [Time frame: Baseline]
  • Muscular elasticity [Time frame: Baseline]
  • Muscular Mechanical Stress Relaxation Time [Time frame: Baseline]
  • Muscular Creep [Time frame: Baseline]
  • Maximal grip strength test [Time frame: Baseline]
  • Muscle fatigue [Time frame: Baseline]
  • Trapeze isometric force [Time frame: Baseline]
  • Muscular Tone [Time frame: 15-30 minutes after training]
  • Dynamic Stiffness [Time frame: 15-30 minutes after training]
Secondary outcome measures (4)
  • Shoulder - passive range of motion [Time frame: Baseline]
  • Cervical spine mobility [Time frame: Baseline]
  • Athletic performance [Time frame: Baseline]
  • History of sports injuries [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

  • Practices swimming or handball 3 to 8 hours per week.
  • Has the cognitive/mental capacity to take part in this study.
  • Fluent in the language of the survey (French).

Exclusion criteria

  • Current orthodontic treatment or treatment completed within the last 2 months.
  • Shoulder and/or cervical spine injury or surgery within the past 6 months.
  • Current cessation or limitation of sports activity due to shoulder and/or cervical symptoms at the time of participation.
  • Any pathology or history of trauma to the dominant hand resulting in reduced grip strength.
  • Any clinically manifest infectious episode at the time of participation.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Belgium · 1 center
  • University of Liège — Liège

Identifiers

NCT: NCT07556211 · 2026/241

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗