Impact of Two Recall Intervals on Dental Caries Incidence, Anxiety and Quality of Life of Preschool Children

Sponsor
University of Sao Paulo (Other)
Overall Status
Completed
CT.gov ID
NCT02263768
Collaborator
(none)
224
1
2
36
6.2

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Oral clinical conditions
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Actual Enrollment :
224 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Prevention
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
Actual Study Start Date :
Mar 1, 2015
Actual Primary Completion Date :
Mar 1, 2018
Actual Study Completion Date :
Mar 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Other: Group 1 - Recall Interval of 12 months

Oral clinical conditions: Caries incidence assessment dental anxiety assessment oral health related quality of life assessment time and costs assessment

Procedure: Oral clinical conditions
Caries incidence assessment dental anxiety assessment oral health related quality of life assessment time and costs assessment
Other Names:
  • Caries incidence
  • dental anxiety
  • oral health related quality of life
  • time and costs
  • Other: Group 2 - Recall Interval of 18 months

    Oral clinical conditions: Caries incidence assessment dental anxiety assessment oral health related quality of life assessment time and costs assessment

    Procedure: Oral clinical conditions
    Caries incidence assessment dental anxiety assessment oral health related quality of life assessment time and costs assessment
    Other Names:
  • Caries incidence
  • dental anxiety
  • oral health related quality of life
  • time and costs
  • Outcome Measures

    Primary Outcome Measures

    1. Dental caries incidence - Change [Baseline, 12 months and 18 months]

      Dental caries will be assessed using the ICDAS criteria (Ismail AI, Sohn W, Tellez M, Amaya A, Sen A, Hasson H, et al. The International Caries Detection and Assessment System (ICDAS): an integrated system for measuring dental caries. Community Dent Oral Epidemiol 2007; 35: 170-8).

    Secondary Outcome Measures

    1. Level of anxiety - Change [Baseline, 12 months and 18 months]

      Level of anxiety will be assessed using the Facial Image Scale (Buchanan H, Niven N. Validation of a facial image scale to assess child dental anxiety. Int J Paediatr Dent 2002;12:47-52).

    2. Oral health related quality of life - Change [Baseline, 12 months and 18 months]

      Oral health related quality of life will be assessed using the Brazilian validation of the ECOHIS (Scarpelli AC, Oliveira BH, Tesch FC, Leão AT, Pordeus IA, Paiva SM. Psychometric properties of the Brazilian version of the Early Childhood Oral Health Impact Scale (B-ECOHIS). BMC Oral Health. 2011; 11:19).

    3. Time [Baseline, 12 months and 18 months]

      The time in minutes, used in the recall interval visits, will be recorded in four categories: time spent on clinical examination including prophylaxis, hygiene and diet orientations, and time spent when the patient miss the recall visit. The total time will correspond to the sum of these categories.

    4. Costs [Baseline, 12 months and 18 months]

      Costs in real (continuous variable) will be recorded in two categories: salary of the dentist and dental assistant paid in public dental services in São Paulo, cost of dental materials/products used in the appointment.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    3 Years to 5 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Dental School of University of São Paulo São Paulo Brazil 05508-000

    Sponsors and Collaborators

    • University of Sao Paulo

    Investigators

    • Study Chair: Marcelo Bönecker, Professor, University of São Paulo

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Gabriela Oliveira Berti, PhD student, University of Sao Paulo
    ClinicalTrials.gov Identifier:
    NCT02263768
    Other Study ID Numbers:
    • 7709191
    First Posted:
    Oct 13, 2014
    Last Update Posted:
    Apr 18, 2019
    Last Verified:
    Jun 1, 2017
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 18, 2019