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Treatment to control Bruxism in adolescent athletes

Effectiveness of two techniques for the management of Bruxism in adolescent athletes: randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7tc89xr
Enrollment
Unknown
Registered
2024-06-24
Start date
2024-02-05
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bruxism, Sleep Bruxism, Facial Pain

Interventions

Randomized clinical trial, four-arm, unblinded. Groups 1 and 2 will receive the intervention for awake bruxism, and groups 3 and 4 for sleep bruxism. Group one: 35 adolescent athletes of both sexes wi

Sponsors

Universidade de Pernambuco
Lead Sponsor
Universidade de Pernambuco
Collaborator

Eligibility

Age
10 Years to 19 Years

Inclusion criteria

Inclusion criteria: Soccer players aged 10-19 years; of both sexes; with definite awake bruxism or possible or probable sleep bruxism associated with a report of orofacial pain or headache

Exclusion criteria

Exclusion criteria: Adolescents Teenagers with a cognitive and/or neurological disorder or syndrome that makes it impossible to complete the questionnaire. Teenagers who utilize an occlusal splint for the management of bruxism and/or temporomandibular dysfunction or any other treatment for orofacial pain in the last twelve months. Teenagers who have used any medications that may affect motor behavior in the three days leading up to the intervention. Adolescents in use of braces

Design outcomes

Primary

MeasureTime frame
Muscle activity: To assess the electromyographic activity of the masticatory muscles (anterior temporalis) utilizing an electromyograph device, where any deviations from the established threshold for each patient are evaluated from the first day of the intervention;Orofacial pain: To assess the frequency and intensity of pain using the DC/TMD diagnostic criteria questionnaire pain module; during the first month of the intervention, the evaluation will be weekly, and after the first month until the end of the 3rd month, the evaluation will be biweekly;Headache: To assess the frequency and intensity of pain using the DC/TMD diagnostic criteria questionnaire pain module; during the first month of the intervention, the evaluation will be weekly, and after the first month until the end of the 3rd month, the evaluation will be biweekly

Secondary

MeasureTime frame
Outcomes secondary are not expected

Countries

Brazil

Contacts

Public ContactFabiana Godoy

Universidade de Pernambuco

fabiana.godoy@upe.br+55(81)3184-7659

Outcome results

None listed

Source: REBEC (via WHO ICTRP)