Toothache
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Children 03 to 13 years of age, with dental pain who seek emergency care in Dental Clinics; Have enough internet for synchronous consultation;Signature of the Informed Consent Form; Have agreed to participate in the research
Exclusion criteria
Exclusion criteria: Do not attend the face-to-face consultation, when allocated in group G2; Problems with the internet;Did not sign the free and informed consent form;Do not agree to participate in the research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to evaluate the presence of dental pain in children and adolescents, considering the independent samples. For the randomized clinical trial, the primary endpoint will be the change in pain score at the 7- and 14-day follow-ups compared to baseline. This outcome is composed of an ordinal qualitative variable and, therefore, the comparison between the telemarketing groups vs. face-to-face consultation will be performed using the Mann-Whitney test. | — |
Secondary
| Measure | Time frame |
|---|---|
| As a secondary outcome, the impact of treatments on oral health-related quality of life and the number of teeth lost after a 24-month follow-up will be evaluated. Differences in the final and initial scores of the oral health-related quality of life questionnaires; and the amount of missing teeth will be compared between groups using Student's t test or the Mann-Whitney test, depending on the normality of the data distribution. | — |
Countries
Brazil
Contacts
FOUSP - Faculdade de Odontologia da Universidade de São Paulo