Predicting Caries Risk in Underserved Toddlers in Primary Healthcare Settings
NCT ID: NCT01707797
Last Updated: 2018-09-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
1326 participants
OBSERVATIONAL
2012-11-15
2017-03-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Healthy children aged 9-15 months
Healthy children aged 12 months (± 3 months) at baseline stratified by Medicaid status and/or race/ethnicity to ensure a diverse representation. Each child will be paired with the primary caregiver, whom the investigators expect to most likely be the adult parent or legal guardian.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* If Primary Caregiver is the Parent/Legal guardian: The parent/legal guardian must provide written informed consent for the child and her/himself (if s/he is the primary caregiver) prior to participation.
* If Primary Caregiver is not the Parent/Legal Guardian: If another individual is the primary caregiver, then this individual must provide written informed consent for her/himself prior to participation.
* The parent/legal guardian and the participating primary caregiver must each be at least 18 years old or an emancipated minor
* The parent/legal guardian must consent and allow examination of the oral cavity of her/his child. The primary caregiver must complete the caries risk assessment questionnaire.
* The primary caregiver must be willing to participate, anticipate being the child's primary caregiver during the study period, and anticipate being available for all examinations (baseline, 18 month follow up, and 36 month follow up), in addition to intermediate contacts in between examinations.
Children
* Child must be 9-15 months of age at the time of the baseline study visit.
* Child must be generally healthy (i.e., no current medical condition that makes it difficult for her/him to receive a dental examination).
* Child must allow examination of the oral cavity.
Exclusion Criteria
* A participant pair (adult-child) who demonstrates an inability to comply with study protocol requirements will be excluded - this determination will be at the Site Primary Investigator's discretion.
* Non-English, non-Spanish reading/speaking individuals will be excluded, as they will not be able to comprehend the consent document or complete the risk questionnaire.
Children
* Children who are in foster care at study initiation will be excluded, due to the likelihood that their primary caregiver will change multiple times during the length of the study.
* Need for antibiotic and/or sedative premedication prior to dental exam.
* Uncontrolled epilepsy.
* Active cancer treatment.
* Unrepaired congenital heart defects that would require premedication prior to dental exam.
9 Months
15 Months
ALL
Yes
Sponsors
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National Institute of Dental and Craniofacial Research (NIDCR)
NIH
University of Michigan
OTHER
Responsible Party
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Margherita Fontana, DDS, PhD
Professor Cariology Discipline Co-coordinator
Principal Investigators
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Margherita Fontana, DDS, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Michigan
Locations
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Indiana University Oral Health Research Institute
Indianapolis, Indiana, United States
University of Iowa
Iowa City, Iowa, United States
Duke Health Center
Durham, North Carolina, United States
Countries
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References
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Fontana M, Eckert GJ, Keels MA, Jackson R, Katz BP, Kemper AR, Levy BT, Levy SM, Yanca E, Kelly S, Daly JM, Patterson B, McKnight P. Predicting Caries in Medical Settings: Risk Factors in Diverse Infant Groups. J Dent Res. 2019 Jan;98(1):68-76. doi: 10.1177/0022034518799080. Epub 2018 Sep 11.
Fontana M, Eckert GJ, Keels MA, Jackson R, Katz B, Levy BT, Levy SM. Fluoride Use in Health Care Settings: Association with Children's Caries Risk. Adv Dent Res. 2018 Feb;29(1):24-34. doi: 10.1177/0022034517735297.
Other Identifiers
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NIDCR 11-101
Identifier Type: -
Identifier Source: org_study_id
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