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Evaluation of the effects of Occlusal Splints and Hypnosis in the treatment of bruxism: A randomized controlled trial

Electromyography and analysis of quality of life in patients with Bruxism before and after treatment with Occlusal Splints, Hypnosis and Restoration of Canine Guidance - randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5s8fy4
Enrollment
Unknown
Registered
2020-07-27
Start date
2018-05-05
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

Interventions

INTERVENTIONS: 1. INTEROCCLUSAL SPLINTS 9 (n = 14): The occlusal splints were made of acrylic according to the laboratory routine in a clinical environment in the following sequence: * First clinical
- Bite registration: - Manufacture of plaster models
- Registration of the facial arch and assembly in semi-adjustable articulator. For such procedures, an approximate time of 20 minutes was required. * Laboratory procedure: - Waxing and making the acr
Device
Behavioural
Other
E03.155.141.481

Sponsors

Universidade Federal dos Vales do Jequitinhonha e Mucuri
Lead Sponsor
Universidade Federal dos Vales do Jequitinhonha e Mucuri
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: elderly patients, presenting reports of waking up with muscle fatigue and / or pain in the TMJ area, with tooth wear and / or edentulous line in the cheek mucosa, reports of noise (teeth grinding) at night evidenced by a partner, being orthognathic, without missing teeth and as few restorations as possible, from a pre-existing database

Exclusion criteria

Exclusion criteria: underage patients, with dental problems with occlusal instability, prognosis and compensation, alcohol, patients with removable prostheses, large amounts of indirect restorations, use of bite plates, neurological or psychiatric disorders, who use drugs that act on the central nervous system, as antidepressant inhibitors of serotonin reuptake, diseases with muscle and / or motor impairment, cognitive impairments and use of illicit drugs.

Design outcomes

Primary

MeasureTime frame
- Muscle electrical activity (EMG), measured by one blinded instructor using a portable equipment (Miotec Equipamentos Biomédicos Ltda, Porto Alegre, RS, Brazil) with analog-digital conversion board of 16-bit model CAD 10/26, sampling frequency of 20-500 kHz. Data collected at the baseline and 40 days after the interventions.;Quality of Life, evaluated by The Oral Health Impact Profile (OHIP-14). Data collected at the baseline and 40 days after the interventions.

Secondary

MeasureTime frame
Pain-related issues, evaluated through a framework of muscle and joint palpation adapted from the Research Diagnostic Criteria (RDC). The average time for completing this procedure was 20 minutes. Data collected at the baseline and 40 days after the interventions.;Stress assessment, evaluated by Lipp’s Inventory, registering the type of symptom (somatic – 37 itens or psychological – 19 itens), and its stage (the alert stage; resistance; close to exhaustion; and exhaustion). This questionnaire is a four-phase stress model, it was validated into Portuguese [Lipp, Lipp 2019]. Data collected at the baseline and 40 days after the interventions.

Countries

Brazil

Contacts

Public ContactAlexandre Henrique Reis Prado

Universidade Federal dos Vales do Jequitinhonha e Mucuri

alexandreprado.cba@gmail.com+55(38)992600113

Outcome results

None listed

Source: REBEC (via WHO ICTRP)