NCT07699263Completed
Effect of an Occlusal Splint in Swimming Performance
Effect of a Customized Occlusal Splint on Athletic Performance in Master Swimmers: A Randomized Pilot Clinical Trial
Source: ClinicalTrials.gov · Last updated 13 Jul 2026
Brief summary (registry, in English)
Optimizing sports performance depends on the interaction of physiological, biomechanical, and neuromuscular factors. In recent years, interest has increased in the relationship between stomatognathic function and athletic performance, particularly regarding the possible role of occlusal splints in neuromuscular activation. This study evaluated the effect of a customized occlusal splint on the increase of Concurrent Activation Potentiation.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 20 (actual)
- First submitted
- 23 Jun 2026
- Start date
- 1 Dec 2025
- Primary completion date
- 30 Apr 2026
- Lead sponsor
- Universidad Europea de Valencia
- Diseases
- Stroke
- NCT number
- NCT07699263
What you commit to
- Study type: Interventional
- Participants enrolled: 20
- From 1 Dec 2025 to the primary completion date, 30 Apr 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Criteria the registry did not label
- To be eligible for inclusion, participants had to be between 20 and 40 years of age, actively participating in regular swimming training, free from acute or chronic injuries, and willing to comply with the study protocol. Exclusion criteria included use of performance-enhancing substances, presence of systemic diseases, current use of medication affecting performance, active orthodontic appliances, temporomandibular joint disorders, pregnancy, or failure to complete the study protocol.
- (It won't let me add the flowchart image, so I'll describe it below)
- Participamos assessed for eligibility (n=24)
- Excluded (n=4) 2.1 Did not Meet inclusion criteria (n=3) 2.2 Did not provide informed consent (n=1)
- Randomized (n=20) 3.1 Intervention group (case) (n=10) 3.1.1 Lost to follow-up (n=0) 3.1.2 Analyzed (n=10) 3.2 Control group (n=10) 3.2.1 Lost to follow-up (n=0) 3.2.2 Analyzed (n=10)
Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Universidad Europea de Valencia Coordinator of this site? Confirm its status | Valencia | Spain | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.