Pandemic-adapted Caries Care Multicentre Single-group Interventional Study

November 28, 2023 updated by: Stefania Martignon, Universidad El Bosque, Bogotá

CariesCare International Adapted for the Pandemic in Children: Caries OUT Multicentre Single-group Interventional Study

The current understanding of dental caries has not been completely transferred into the clinical practice to control caries lesion progression (severity / activity) and the individual risk of caries. This situation led to the development of the CariesCare International CCI Caries Management System (2018), derived from ICCMS™- International Caries Classification and Management System (2012) and the ICDAS - International Caries Detection and Assessment System (2002) in a consensus among more than 45 cariologists, epidemiologists, public health professionals, researchers and cliniciansfrom all over the world. The consensus aimed to guide dentists and dental teams in clinical practice, facilitating the control of the caries process and the maintenance of oral health in their patients.

The general lack of implementation of an updated management of dental caries is evident in Colombia, in the survey of 1094 clinicians, teachers and students, failures were reported to adopt related behaviours, motivation barriers (remuneration), opportunity (in terms of relevance, physical/infrastructure resources, time) and training. As an additional barrier, the Colombian Chapter of the Alliance for a Cavity-Free Future (ACFF), evidences the absence of a facilitating Oral Health Record (OHR), this situation lead to stablish a new Alliance between the Ministry of Health and Social Protection (MSPS) and the AFLC to develop an inter-institutional consensus at the national level, of a clinical history for diagnosis and management of lesions and caries risk. Finally, 55 institutions participated in this consensus, and we have just finished a pilot test of the forms to submit a proposal for national standardization from the MSPS.

The aim of this multicentre case series is to assess after 3, 6 and 12 months in children oral health outcomes, caregivers' satisfaction and in dentists' process outcomes, after the implementation of the CCI system adapted for the COVID-19 era -non-aerosol generating procedures. Oral health outcomes will be evaluated in terms of:

  • Effectiveness of CCI to control bacterial plaque, caries progression and caries risk, and to achieve behavioural change in oral health in children.
  • Acceptance of CCI caries management adapted for COVID-19 through Treatment Evaluation Interventory in dentists, and in children/parents through satisfaction questionnaire.
  • Costs of CCI adapted for caries management, in economic terms, number and appointment time.

Study Overview

Detailed Description

This study has been planned to be developed in 21 centres: 5 Colombian, 14 international dental schools, 1 Colombian health care provider and a demonstrative centre of the ACFF. Each center will implement the CCI management adapted for COVID-19 era in a total of 20 3 to 5- and 6 to 8-year-old children. Children's caries care can be delivered at dental schools' clinics and private practice. Follow-up assessments will be conducted at 3, 6 and 12 months.

Study Type

Observational

Enrollment (Actual)

409

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Buenos Aires, Argentina
        • Universidad de Buenos Aires
      • Córdoba, Argentina
        • Universidad Nacional de Córdoba
      • São Paulo, Brazil
        • University of Sao Paulo
      • Barranquilla, Colombia
        • Viva 1A IPS Health Provider
      • Bogotá, Colombia
        • Fundación Universitaria de Colegios de Colombia
      • Cartagena, Colombia
        • Corporación Universitaria Rafael Núñez
      • Cartagena, Colombia
        • Universidad de Cartagena
      • Manizales, Colombia
        • ACFF Colombian Chapter Manizales Demonstration Territory
      • Medellín, Colombia
        • Universidad Cooperativa de Colombia
    • Bogotá DC
      • Bogotá, Bogotá DC, Colombia, 110121
        • Universidad El Bosque
      • Santo Domingo, Dominican Republic
        • Universidad Iberoamericamericana
      • Nice, France
        • Universite Cote d' Azur
      • Guadalajara, Mexico
        • Universidad de Guadalajara
      • Amsterdam, Netherlands
        • ACTA
      • Lima, Peru
        • Universidad Peruana Cayetano Heredia
      • Porto, Portugal
        • University of Porto
      • Moscow, Russian Federation
        • University of Moscow
      • Sheffield, United Kingdom
        • University of Sheffield
    • Indiana
      • Indianapolis, Indiana, United States, 47405
        • Indiana University
    • Massachusetts
      • Boston, Massachusetts, United States, 02155
        • Tufts University
    • Sanmartin
      • Buenos aires, Sanmartin, Uruguay
        • Universidad Catolica de Uruguay

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

3 years to 8 years (Child)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Participants will be enrolled from the University Dental clinics, dental health providers and dental private practice across 21 multi-centre sites. The parents/caregivers of patients, aged 3 to 5 years and 6 to 8 years will be invited by the dentist to participate in the study and that their children are eligible to be considered for recruitment.

Description

Inclusion Criteria:

  • Children 3 to 5 and 6 to 8 years of age.

Exclusion Criteria:

  • Family plans to move during the study time
  • Oral-health related systemic conditions or physical/mental disabilities
  • Presence of orthodontic/orthopaedic appliances
  • Presence of MIH in first permanent molars with indication of extraction
  • Children attending for a dental emergency/urgency

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Adapted-CCI single-intervention group in children
The single-group intervention will be the adapted-CCI 4D-cycle caries care, with non-AGP and reduced in-office appointments' time. A trained examiner per centre will conduct examinations at baseline, at 5-5.5 months (three months after basic management), 8.5 and 12 months, assessing the child's CCI caries risk and oral-health behaviour, visually staging and assessing caries-lesions severity and activity without air-drying (ICDAS-merged Epi); fillings/sealants; missing/dental-sepsis teeth, and tooth symptoms, synthetizing together with parent and external-trained dental practitioner (DP) the patient- and tooth-surface level diagnoses and personalised care plan. DP will deliver the adapted-CCI caries care. Parents' and dentists' process acceptability will be assessed via Treatment-Evaluation-Inventory questionnaires, and costs in terms of number of appointments and activities. Twenty-one centres in 13 countries will participate.

Interventions of this single-group study correspond to the 4D, to be implemented by the external DP, when possible with remote care and only with non-AGP:

  1. D-DETERMINE risk assessing the protective and risk factors (social/medical/behavioural and clinical), using remote tools. Additionally, the description of tooth brushing behaviours and consumption of free sugars is included.
  2. D-DETECT & ASSESS: Caries staging and activity: ICDAS-merged visual criteria Caries OUT (without using compressed air, and avoiding radiographs). Clinical risk factors are assessed as well.
  3. D-DECIDE a personalized care plan: individually designed for caries management home and clinical approaches.
  4. D-DO: Appropriate Tooth-preserving & Patient-level caries: Management plan at the Patient and at the Lesion level and the implementation of the Change Behaviour Tool (CBT) designed for this protocol.

The follow-up data will include a T1, T2 and T3 assessment.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mean number of tooth surfaces with avoidance of caries progression (ICDAS-merged Epi severity and/or activity)
Time Frame: up to 12 months
With the implementation of the CCI 4D-cycle adapted for the COVID-19 pandemic characterized by the patient-centred risk -based caries management systems, the the primary outcomes consist of: At the tooth surface level in avoidance of individuals and average number of surfaces with caries progression. At the individual level consist in avoidance of caries risk level increase/no control, plaque control, and avoidance of extraction, pain, failure of the restoration. Figures will be described using mean and standard deviation (SD) for quantitative variables and percentages for qualitative variables.
up to 12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Proportion of subjects with avoidance of caries progression (ICDAS-merged Epi severity and/or activity)
Time Frame: up to 12 months
Figures will be described using mean and standard deviation (SD) for quantitative variables and percentages for qualitative variables.
up to 12 months
Proportion of subjects with avoidance of caries risk level increase/no control, and avoidance of extraction, pain, failure of the filling/sealant.
Time Frame: up to 12 months
Figures will be described using mean and standard deviation (SD) for quantitative variables and percentages for qualitative variables.
up to 12 months
Proportion of parents and dentists with high dental care process acceptability (measured with TEI).
Time Frame: up to 12 months
Figures will be described using mean and standard deviation (SD) for quantitative variables and percentages for qualitative variables.
up to 12 months
Proportion of subjects with avoidance of caries risk level increase/no control, and avoidance of extraction, pain, failure of the filling/sealant
Time Frame: up to 12 months
Figures will be described using mean and standard deviation (SD) for quantitative variables and percentages for qualitative variables.
up to 12 months
Proportion of children improving oral-health related behaviours
Time Frame: up to 12 months
Figures will be described using mean and standard deviation (SD) for quantitative variables and percentages for qualitative variables.
up to 12 months
Description of dental care costs
Time Frame: up to 12 months
The providers' payment model of the centre will be described (Fee-for-service, Capitation, Salary-based and Pay-for-performance) (43). For the description of costs, these will be converted to the United States Dollar (USD) under the average Market Representative Exchange Rate for the year 2021 (MRER-average).
up to 12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Stefania Martignon, PhD, Universidad El Bosque

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 15, 2020

Primary Completion (Actual)

December 30, 2021

Study Completion (Actual)

December 30, 2021

Study Registration Dates

First Submitted

December 7, 2020

First Submitted That Met QC Criteria

December 7, 2020

First Posted (Actual)

December 14, 2020

Study Record Updates

Last Update Posted (Estimated)

December 4, 2023

Last Update Submitted That Met QC Criteria

November 28, 2023

Last Verified

November 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

All IPD

IPD Sharing Time Frame

CariesCare International adapted for the pandemic in children: Caries OUT multicentre single-group interventional study protocol

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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