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

Construction of a Multidimensional Risk Prediction Model for Severe Early Childhood Caries Based on the "Bio-psy-social" Medical Model

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.

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Detailed Description

Severe Early Childhood Caries (S-ECC), as a serious infectious disease that severely endangers the physical and mental health of preschool children, has now become a major public health challenge in pediatric dentistry in China. Epidemiological data show that the prevalence of caries among 3-5-year-old children in China remains high, and it is characterized by rapid disease progression, extensive tooth surface involvement, and high treatment difficulty. S-ECC not only leads to extensive tooth tissue loss in children, causing severe pain due to pulpitis and periapical inflammation, but also seriously affects children's masticatory efficiency, facial growth and development, language function, and sleep quality, and may even induce systemic diseases due to long-term chronic inflammation. Although current clinical treatment methods cover fluoride application, minimally invasive restoration, and comprehensive treatment under general anesthesia, high postoperative recurrence rates and difficult behavioral management are common problems in clinical practice. This reveals the limitations of the current "biomedical model" dominated diagnosis and treatment system, which focuses on the repair of dental lesions but neglects the deep-seated family behavioral and psychosocial roots that cause the disease and its recurrence.

Previous research on the etiology of S-ECC mainly focused on biological aspects such as cariogenic bacteria (such as Streptococcus mutans), host factors (such as saliva composition and tooth structure), and environmental factors (such as sugar intake frequency) . With the deepening of research, although some scholars have begun to pay attention to the impact of socioeconomic status (SES) on oral health, finding that parents' educational level and family income are significantly related to the caries rate, these macroscopic sociodemographic indicators are difficult to explain why there are significant differences in oral health management capabilities among families with similar socioeconomic backgrounds . The current knowledge gap lies in the lack of analysis of the family aggregation mechanism of S-ECC from the perspective of micro psychology and behavioral neuroscience. In particular, the concept of "parental burnout" proposed in the field of psychology in recent years, which refers to the emotional exhaustion and reduced parental efficacy that parents experience under long-term parenting stress, may lead to the lack or ineffectiveness of their supervision over children's oral hygiene behaviors, but this has not been fully verified in the field of dentistry . At the same time, previous studies often viewed dietary habits in isolation and ignored the "24-hour activity behavior" holistic view proposed by the World Health Organization, that is, there may be complex interactions between sleep disorders (such as mouth breathing, night waking), sedentary behavior (excessive screen time), and unhealthy diet, which together form a risk loop for S-ECC. In addition, the cognitive traits of preschool children themselves, such as deficits in inhibitory control in executive function, may lead to poor cooperation in tooth brushing and poor control of dietary impulses, and the impact of this neuro-psychological characteristic on the susceptibility to S-ECC is also a blind spot in current research.

Given the above background and research status, it is particularly urgent and important to conduct multi-dimensional risk factor research on S-ECC in preschool children based on the "biopsychosocial" medical model. This study aims to break through the framework of traditional etiological research, and on the basis of collecting objective clinical indicators such as the dmft index and plaque index, introduce psychological and behavioral science assessment tools to systematically explore the deep association pathways between parental burnout, children's executive function deficits, and unhealthy lifestyles (sleep, screen time) and the onset of S-ECC. This study not only helps to fill the current knowledge gap regarding the psychosocial pathogenesis of S-ECC and explain the phenomenon that "high-knowledge families" may still have a high risk of caries, but also has important clinical translation significance. By constructing a multi-dimensional risk prediction model of S-ECC that incorporates psychological and behavioral characteristics, clinicians can identify families with "high-risk psychological and behavioral characteristics" at an early stage, thereby moving the intervention point forward and achieving a shift from merely "tooth treatment" to "overall oral health management of the family". This provides a solid evidence-based medical basis for formulating precise personalized prevention strategies and reducing the recurrence rate of S-ECC.

Study Type

Observational

Enrollment (Estimated)

1200

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

  • Child

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

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

Description

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  • 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;
  • Refusing to undergo oral clinical examination or unable to cooperate.

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
number of carious teeth at the baseline
Time Frame: at the baseline
The number of the carious teeth includes the treated or untreated carious teeth.
at the baseline
number of carious teeth at 6 months
Time Frame: at 6 months after enrollment
The number of carious includes treated or untreated carious teeth.
at 6 months after enrollment
number of carious teeth at 1 year
Time Frame: at 1 year after enrollment
the number of carious teeth includes treated or untreated carious teeth.
at 1 year after enrollment

Collaborators and Investigators

This is where you will find people and organizations involved with this 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 (Estimated)

March 1, 2026

Primary Completion (Estimated)

May 30, 2027

Study Completion (Estimated)

May 30, 2028

Study Registration Dates

First Submitted

December 24, 2025

First Submitted That Met QC Criteria

January 12, 2026

First Posted (Actual)

January 13, 2026

Study Record Updates

Last Update Posted (Actual)

February 12, 2026

Last Update Submitted That Met QC Criteria

February 10, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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