Overview

This trial is active, not recruiting.

Conditions dental caries, quality of life, anxiety
Treatment oral clinical conditions
Sponsor University of Sao Paulo
Start date September 2014
End date May 2017
Trial size 224 participants
Trial identifier NCT02263768, 7709191

Summary

Objectives: To assess the effectiveness of two recall intervals on dental caries incidence (primary outcome) in preschool children with low and moderate caries risk. The level of anxiety, oral health related quality of life (OHRQoL), time and cost (secondary outcomes) according to each interval will also be assessed. Methods: The sample will consist of 224 children between 3-5 years of age, of both genders, with low and moderate caries risk according to the clinical criteria adapted from the Secretary of Health of São Paulo. Children will be randomly allocated into two study groups: Group 1 (G1) - oral clinical examination + orientation for oral health and diet on the recall of 12 months; and Group 2 (G2) - oral clinical examination + orientation for oral health and diet on the recall of 18 months.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Intervention model parallel assignment
Masking single blind (investigator)
Primary purpose prevention
Arm
(Other)
Oral clinical conditions: Caries incidence assessment dental anxiety assessment oral health related quality of life assessment time and costs assessment
oral clinical conditions Caries incidence
Caries incidence assessment dental anxiety assessment oral health related quality of life assessment time and costs assessment
(Other)
Oral clinical conditions: Caries incidence assessment dental anxiety assessment oral health related quality of life assessment time and costs assessment
oral clinical conditions Caries incidence
Caries incidence assessment dental anxiety assessment oral health related quality of life assessment time and costs assessment

Primary Outcomes

Measure
Dental caries incidence - Change
time frame: Baseline, 12 months and 18 months

Secondary Outcomes

Measure
Level of anxiety - Change
time frame: Baseline, 12 months and 18 months
Oral health related quality of life - Change
time frame: Baseline, 12 months and 18 months
Time
time frame: Baseline, 12 months and 18 months
Costs
time frame: Baseline, 12 months and 18 months

Eligibility Criteria

Male or female participants from 3 years up to 5 years old.

Inclusion Criteria: - Children between 3-5 years of age, of both genders, with low and moderate caries risk according to the clinical criteria adapted from the Secretary of Health of São Paulo. - Guardians who have signed the informed consent confirming their participation and their child in research. Exclusion Criteria: - Children showing visible dental plaque and gingivitis in baseline. - Children showing more than 08 active and/or inactive caries cavitated surfaces, and who show fistula and/or dental abscess. - Special patients. - Children who received professional application of fluoride in the 6 months prior to the survey.

Additional Information

Official title Impact of Two Recall Intervals Associated to Oral Health Counseling on Dental Caries Incidence, Anxiety and Quality of Life of Preschool Children With Low and Moderate Caries Risk: Randomized Clinical Trial
Description An examiner calibrated and blinded to the study groups and the secondary outcomes will perform the clinical examinations, which consist of: the gingival bleeding index, dental plaque index, detection of caries and its activity according to the ICDAS (International Caries Detection and Assessment System) and the clinical features of active and inactive caries lesions will be associated with the criteria discribed in ICDAS Commitee manual. An external dentist will conduct the assessment of the anxiety levels assessed by the Facial Image Scale, the OHRQoL measured by B-ECOHIS (Brazilian Early Childhood Oral Health Impact Scale), the time and costs. All groups will be followed for a period of 36 months. All analyzes will be performed with the intention of treatment (ITT) and considering the sensitivity analyzes to assess the differences between the ITT analyzes and the complete cases analyzes.
Trial information was received from ClinicalTrials.gov and was last updated in November 2016.
Information provided to ClinicalTrials.gov by University of Sao Paulo.