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Short-term effects of a Rigid Interocclusal Appliance and Hypnosis on individuals with bruxism: a feasibility study for a randomized clinical trial

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This study had the aim of evaluate the feasibility of a randomized clinical trial to compare the effects of a Rigid Interocclusal Appliance and Hypnosis on the quality of life and muscle pain in individuals with bruxism. Forty-two patients with self- report bruxism and clinical examination were randomly assigned to three groups: Rigid Interocclusal Appliance (G1), Hypnosis (G2), and a Control Group (G3). Data collection occurred at baseline and 40 days after the interventions using the Oral Health Impact Profile (OHIP-14), Lip’s Inventory of Stress Symptoms (ISSL) and muscle and joint palpation. P-value < 0.05 was considered significant. The G1 showed a greater reduction in pain in the masseter’s portions and in the temporalis tendon insertion (p<0.05). No significant differences were observed in the quality of life (OHIP-14). From this pilot study it was possible to verify the feasibility of a clinical trial with a larger sample size and follow-up time.
Title: Short-term effects of a Rigid Interocclusal Appliance and Hypnosis on individuals with bruxism: a feasibility study for a randomized clinical trial
Description:
This study had the aim of evaluate the feasibility of a randomized clinical trial to compare the effects of a Rigid Interocclusal Appliance and Hypnosis on the quality of life and muscle pain in individuals with bruxism.
Forty-two patients with self- report bruxism and clinical examination were randomly assigned to three groups: Rigid Interocclusal Appliance (G1), Hypnosis (G2), and a Control Group (G3).
Data collection occurred at baseline and 40 days after the interventions using the Oral Health Impact Profile (OHIP-14), Lip’s Inventory of Stress Symptoms (ISSL) and muscle and joint palpation.
P-value < 0.
05 was considered significant.
The G1 showed a greater reduction in pain in the masseter’s portions and in the temporalis tendon insertion (p<0.
05).
No significant differences were observed in the quality of life (OHIP-14).
From this pilot study it was possible to verify the feasibility of a clinical trial with a larger sample size and follow-up time.

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