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CompletedNCT07882914Updated Oct 20, 2026

Dental Anxiety in Children Attending Emergency Versus Routine Dental Care

An observational study in Dental Anxiety and Dental Fear, sponsored by Marmara University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 2 Years to 13 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-20.

Sponsored by Marmara University · Observational

Updated Oct 20, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
47
Ages
2 Years to 13 Years
Sex
All
01

Study summary

The goal of this observational study is to learn whether children who come to a pediatric dental emergency clinic have higher dental anxiety than children who come for routine dental care. The study includes children aged 2 to 13 years attending the Department of Pediatric Dentistry at Marmara University in Istanbul, Turkiye.

The main question it aims to answer is: Do children attending an emergency dental visit (because of dental pain, abscess, facial swelling, or dental trauma) have higher dental anxiety scores than children attending a routine dental visit?

Researchers will also look at whether dental anxiety is related to age, sex, previous dental visits, previous local anesthesia, and tooth decay experience.

Participants will:

  • Have a parent or guardian fill out a short form about the child's age, sex, and dental history
  • Receive a routine dental examination to record tooth decay (dmft/DMFT index)
  • Answer the 4-question Turkish version of the Corah Dental Anxiety Scale during a single visit

No extra treatment or intervention is given as part of this study.

Read the detailed description

Dental fear and anxiety are common in children and are a major barrier to dental care. Dental pain and traumatic dental injuries are the leading reasons for emergency dental visits in children, but few studies have directly compared dental anxiety between children attending emergency and routine dental care.

This single-center, cross-sectional pilot study was conducted at the Department of Pediatric Dentistry, Marmara University Faculty of Dentistry. Children were allocated to two groups according to the type of visit: (1) Emergency group: children presenting to the pediatric emergency dental clinic with pain due to acute apical abscess, facial swelling, dental trauma, or similar urgent conditions; (2) Routine group: children presenting for routine examination or treatment without dental pain, trauma, or acute infection.

After written informed consent was obtained from parents or legal guardians, parents completed a questionnaire on demographic characteristics and dental history (previous dental visits, previous treatments, pain experience, local anesthesia or sedation history). Caries experience was recorded using the WHO dmft/DMFT index. Dental anxiety was measured with the Turkish version of the Corah Dental Anxiety Scale (C-DAS; 4 items, total score 4-20).

Statistical analysis was performed with IBM SPSS Statistics v24. Normality was assessed with the Shapiro-Wilk test; group comparisons used the independent samples t-test or Mann-Whitney U test, and categorical variables were compared with the Chi-square test. Correlations were evaluated with Pearson or Spearman analyses. Statistical significance was set at p\<0.05.

The original protocol planned to include 106 participants; 47 children were enrolled during the data collection period, and the study was therefore reported as a pilot study.

02

Conditions studied

  • Dental Anxiety
  • Dental Fear

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Keywords

  • Pediatric Dentistry
  • Emergency Dental Care
  • Corah Dental Anxiety Scale
  • Children
  • Dental Caries
03

In context

Dental Caries

1,137 studies on the registry are indexed under Dental Caries; 201 are open to participants now.

This study's enrollment of 47 is below the median of 178 across 185 observational studies indexed under Dental Caries.

Browse Dental Caries studies →

Lead sponsor

Marmara University is the lead sponsor of 589 studies on the registry; 136 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
2 Years to 13 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Children aged 2-13 years attending the Department of Pediatric Dentistry, Marmara University Faculty of Dentistry, Istanbul, Turkiye, either at the pediatric emergency dental clinic (dental pain, acute apical abscess, facial swelling, or dental trauma) or at the routine pediatric dental clinic, enrolled consecutively during the study period.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Children aged 2-13 years
  • Written informed consent provided by a parent or legal guardian
  • Admission to either the pediatric dentistry clinic or the pediatric emergency dental clinic
  • Ability to communicate effectively with the researchers
  • Absence of mental or cognitive disabilities
  • Emergency group: attending the faculty for the first time with acute apical abscess, facial swelling, dental trauma, or similar urgent dental conditions (children who previously received dental treatment at other centers were also eligible)
  • Routine group: attending for routine examination or treatment without dental pain, trauma, or acute infection at admission

Exclusion criteria

Exclusion Criteria:

  • Failure to obtain written informed consent from a parent or legal guardian
  • Inability to communicate with the researchers or severe communication barriers
  • Presence of mental or cognitive disabilities
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
47 participants (actual)
Patient registry
No

Groups and cohorts

  • Emergency Dental Care Group

    Children aged 2-13 years presenting to the pediatric emergency dental clinic with dental pain due to acute apical abscess, facial swelling, dental trauma, or similar urgent conditions, attending the faculty for the first time.

  • Routine Dental Care Group

    Children aged 2-13 years presenting to the pediatric dentistry clinic for routine examination or treatment, with or without prior dental experience, and without dental pain, trauma, or acute infection at the time of admission.

06

What researchers measure

Primary outcomes

  1. Dental Anxiety Score (Corah Dental Anxiety Scale)

    Dental anxiety was assessed using the Turkish version of the Corah Dental Anxiety Scale (C-DAS), a 4-item questionnaire with each item scored from 1 to 5. Total scores range from 4 to 20, with higher scores indicating greater dental anxiety. Mean C-DAS scores were compared between the emergency and routine dental care groups.

    Time frame: Day 1 (before clinical examination)

Secondary outcomes

  1. Distribution of Dental Anxiety Categories

    Participants were categorized according to total C-DAS score (not anxious: 0-4, low anxiety: 5-8, moderate anxiety: 9-12, high anxiety: 13-14, extreme anxiety/phobia: 15-20). The proportion of participants in each category was compared between groups.

    Time frame: Day 1 (before clinical examination)

  2. Caries Experience (dmft/DMFT Index)

    Caries experience was recorded by clinical examination using the WHO dmft/DMFT index (number of decayed, missing, and filled primary/permanent teeth). Higher scores indicate greater caries experience.

    Time frame: Day 1 (at clinical examination)

07

Study locations

1 site
  • Marmara University Faculty of Dentistry
    Istanbul, 34854, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No — Individual participant data will not be shared publicly because participants are minors and the informed consent obtained from parents/legal guardians did not include data sharing. Aggregated data are reported in the publication; anonymized data may be made available by the corresponding author upon reasonable request and with ethics committee approval.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 20, 2026
Show all 1 update
  1. Oct 20, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07882914
Lead sponsor
Marmara University
Responsible party
Sponsor
First posted
Oct 20, 2026
Start date
Mar 15, 2025
Primary completion
May 15, 2025
Completion
May 15, 2025
Last update
Oct 20, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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