Construction of a Multidimensional Risk Prediction Model for Severe Early Childhood Caries

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age3-6
SponsorThe Children's Hospital of Zhejiang University School of Medicine

About this trial

This study aims to address the high prevalence and recurrence rate of severe early childhood caries (S-ECC) by breaking away from the traditional single biological factor perspective and introducing the theories of "24-hour activity behavior" and "family psychological stress". By collecting clinical and behavioral data from 1,200 preschool children and their parents, it explores the association pathways between parental burnout, children's executive function, sleep/dietary behaviors and S-ECC, and builds a high-precision risk prediction model to provide evidence-based support for the clinical development of personalized prevention strategies.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age range: 3-6 years old (36 months ≤ months < 72 months);

Good overall health condition (ASA classification I-II);

Parents have given informed consent and are willing to participate in this study.

Disqualifiers

Suffering from severe systemic diseases (such as congenital heart disease, blood disorders, immune deficiencies, etc.);

Having congenital craniofacial deformities (such as cleft lip and palate, facial clefts, etc.);

Undergoing orthodontic treatment for the mouth;

Having a history of long-term use of drugs that affect saliva secretion;

Trial population

Children who visited the oral department of the Children's Hospital affiliated to Zhejiang University School of Medicine.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • questionnaire survey

    Other intervention

    Parents fill out the "Children's Oral Health and Comprehensive Development Assessment Form", which includes scales such as family socioeconomic status, parental burnout in child-rearing (PBA), children's executive function (BRIEF-P), sleep habits (CSHQ), and dental fear (CFSS-DS).

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

number of carious teeth at the baseline

The number of the carious teeth includes the treated or untreated carious teeth.

Time frame
at the baseline
2

number of carious teeth at 6 months

The number of carious includes treated or untreated carious teeth.

Time frame
at 6 months after enrollment
3

number of carious teeth at 1 year

the number of carious teeth includes treated or untreated carious teeth.

Time frame
at 1 year after enrollment

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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