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Ferula DeportivaNCT07523984

Effects of a Training Oral Device (Custom Splint) Adjusted Using Electromyography for the Balance Between the Masseter and Temporal Muscle in Elite Military Paratroopers.

A study testing Effects of a Training Oral Device (Custom Splint) Adjusted Using Electromyography in people with Ferula Deportiva, run by Universidad Católica San Antonio de Murcia at 1 site in Spain.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The aim of this prospective, longitudinal observational study is to evaluate the influence of the use of sports splints on the muscular activity of the stomatognathic system and cervical mobility in adult sport parachutists. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Ferula Deportiva
What is being tested?
Effects of a Training Oral Device (Custom Splint) Adjusted Using Electromyography
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
19 participants
Where
1 siteSpain
Study dates
1 Dec 2020to 28 Feb 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Athletes aged 18 years or older
  • good oral health -no history of cardiovascular disease or diabetes -
  • oral hygiene habits of at least two brushings per day.

Who cannot join

  • Poor oral hygiene periodontitis history of recent dental trauma.

Trial locations and contacts

1 site in 1 country.

Spain1 site
  • UCAM DENTAL Av. Juan Carlos I 30008 Murcia (en el CC ZigZag)

    Murcia, Murcia, 30008

Other trials in Spain

About this study

Official title: Comparative Study in Professional Paratroopers Between Occlusion and Postural Condition

The aim of this prospective, longitudinal observational study is to evaluate the influence of the use of sports splints on the muscular activity of the stomatognathic system and cervical mobility in adult sport parachutists.

The main research questions are: Does the use of a sports splint modify the electromyographic activity of the masticatory muscles during functional movements? Does it produce changes measurable by accelerometry?

Read more

The researchers will compare the records obtained with and without the sports splint in order to determine whether the use of this device produces changes in the neuromuscular activity of the stomatognathic system and in cervical mobility.

Participants will perform the following tasks during the evaluation:

Recording of electromyographic activity of the masticatory muscles using surface electromyography.

Measurement of cervical movements using an accelerometer. Performance of functional cervical movements (flexion, extension, lateral inclination, and nodding) under conditions with and without the sports splint.

Being tested
Effects of a Training Oral Device (Custom Splint) Adjusted Using Electromyography

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Effects of a Training Oral Device (Custom Splint) Adjusted Using ElectromyographyDiagnostic test

    Electromyographic recording comparing muscle activity with and without a sports splint.

Study groups in NCT07523984
Study groupRoleWhat they receive
Condición "splint-off" Condición "splint-on"Active comparatorEach participant acted as their own control, with EMG recorded without and with the sports splint.
Receives: Diagnostic Test: Effects of a Training Oral Device (Custom Splint) Adjusted Using Electromyography

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. POC TA

    Percentage of Overlapping Coefficient of the Anterior Temporalis (right and left): A parameter that measures the degree of overlap in electromyographic activity between two muscles or between two conditions, used to assess muscular coordination or symmetry. The higher the percentage, the more synchronized or similar the muscular activity.

    Measured: 2 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Apr 2026
  2. Study start1 Dec 2020
  3. Primary completion10 Aug 2025
  4. Study completion28 Feb 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
19 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07523984
Sponsor's protocol ID
CE112008
Other IDs
CE112008
Status last verified
Apr 2026
First submitted
19 Mar 2026
Last updated
13 Apr 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Effects of a Training Oral Device (Custom Splint) Adjusted Using Electromyography in people with Ferula Deportiva, run by Universidad Católica San Antonio de Murcia at 1 site in Spain.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 13 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

POC TA (time frame: 2 year). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Apr 2026.

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