Sleep bruxism
Conditions
Interventions
Intervention content for the intervention group
During the intervention period (3 weeks), the study subjects will be provided with three low-fiber meals (boxed lunches), a research beverage containing
Sponsors
Daisuke Ekuni
Toyama Naoki
Nagase Viita Co., Ltd.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: The subjects are Japanese people aged 18 years or older who are healthy and have sleep bruxism and do not require medical treatment at a hospital. Patients who have received a full explanation of this study and who are able to provide written consent to participate in the study of their own free will.
Exclusion criteria
Exclusion criteria: Smokers Excessive alcohol drinkers (average of 20g or more of pure alcohol per day) Those taking calcium antagonists and selective serotonin reuptake inhibitors Those with insomnia or those who regularly use sleeping pills Those who are obese or underweight Those who have taken antibiotics within 3 months of starting the study Those with food allergies Pregnant women or women who may be pregnant Breastfeeding women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in the number of sleep bruxism incidents per hour | — |
Secondary
| Measure | Time frame |
|---|---|
| Intestinal flora, fecal short-chain fatty acid content, objective sleep quality, subjective sleep quality | — |
Contacts
Public ContactEkuni Daisuke
Graduate School of Medicine, Dentistry and Parmaceutical Sciences, Okayama University
Outcome results
None listed