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CompletedNCT05563532Updated Oct 3, 2022

Dental Anxiety and Periodontal Health

An observational study in Dental Anxiety, Periodontal Health and Oral Hygiene, sponsored by Okan University. Completed at 1 site in Turkey. Open to participants aged 4 Years to 12 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-10-03.

Sponsored by Okan University · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
280
Ages
4 Years to 12 Years
Sex
All
01

Study summary

Mothers usually have the primary role in bringing up children and developing health-related behaviors. The aim of this study was to determine the effect of mothers' dental anxiety and oral hygiene on the dental anxiety and periodontal health of their children.

The study included 280 randomly selected children, aged 4-12 years, who came to the dentist for the first time and their mothers. Demographic and oral hygiene information of the mothers was collected through a questionaire. Dental anxiety of the mothers and children was assessed using the Modified Dental Anxiety Scale (MDAS) and the Venham Picture Test (VPT), respectively.

Read the detailed description

Anxiety is a neurotic syndrome in which patients have difficulty in explaining internal restlessness, anxiety and fear reaching the level of panic, which causes physiological and behavioral disorders as a result of affecting motor tension and even autonomic hyperactivity. Anxiety and fear are frequently encountered in dentistry clinical practice in both adults and children. Dental anxiety is also defined as intense fear and anxiety that occurs as a result of the thought that patients will be harmed, that they will have an unknown operation outside their control, and because they have had previous negative dental treatment experiences.

Direct factors such as previous traumatic dental experiences, postoperative complications, age, gender, anxious temperament in childhood, and indirect factors such as the effect of family on the approach to dental treatment and sociodemographic factors have been reported to have an effect on the development of dental anxiety. Most early school-age children begin to imitate their parents as role models. Children in this age group internalize their mothers' values, attitudes and behaviors, since they usually spend more time with their mothers. It is thought that especially parents' dental anxiety may have an effect on their children's dental anxiety through modeling and knowledge.

Children with dental anxiety try every way to avoid dental treatment. The thought that patients will feel more pain than normal due to the anxiety they experience during dental treatments makes treatment difficult. Anxiety might lead to individuals discontinuing treatment, thereby worsening their dental health. As a result, necessary dental treatment becomes more time-consuming, invasive, and costly. At the same time, treatment anxiety impedes the clinical process, jeopardizes treatment results, and causes professional stress for dentists.

Dental anxiety is evaluated through projective tests, behavioral assessments, psychometric assessments, and physiological techniques. Behavioral assessment is based on the dentist or researchers scoring the behaviors visually. For this purpose, the Frankl Behavior Scale and the Yale Preoperative Anxiety Scale are used. Psychometric assessments are made with questionnaires, which are the most preferred because of their ease of application, and these are used to measure the anxiety of children or adults before dental treatment. At the present time, the Modified Dental Anxiety Scale (MDAS) is frequently used for adults, while the Children's Fear Survey Schedule-Dental Subscale (CFSS-DS) is used for children. Projective techniques also use pictures or narratives of objects that may cause anxiety and fear in young children. The Venham Picture Test (VPT) and Children's Dental Fear Picture Test are commonly used projective techniques. Physiological techniques measure anxiety-related parameters such as salivary cortisol level, blood pressure, and dorsal skin response. However, it is thought that the equipment used in this technique may increase anxiety, especially in children.

From a review of literature it can be seen that there are few studies conducted in Turkey which have evaluated the effect of the mother on the child's dental anxiety and oral hygiene. The aim of this study was to determine the effects of mothers' dental anxiety and oral hygiene on the dental anxiety and periodontal health of their children, using psychometric analysis and projective methods.

02

Conditions studied

  • Dental Anxiety
  • Periodontal Health
  • Oral Hygiene

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03

In context

Anxiety Disorders

4,868 studies on the registry are indexed under Anxiety Disorders; 1,390 are open to participants now.

This study's enrollment of 280 is above the median of 150 across 606 observational studies indexed under Anxiety Disorders.

Browse Anxiety Disorders studies →

Lead sponsor

Okan University is the lead sponsor of 96 studies on the registry; 14 are open to participants now.

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

04

Who can participate

Ages eligible
4 Years to 12 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study inclusion criteria for mothers were the absence of any systemic and psychiatric disorders, not being pregnant or breastfeeding, non-smoking, not having received periodontal treatment in the last 6 months, and with at least 20 teeth and willing to participate in the study. The inclusion criteria for children were defined as age 4-12 years, having no known systemic disease, visiting a dentist for the first time, and not having reported acute pain. Only one child per family was included in the study for mother-child pairs.

Inclusion criteria

  • The inclusion criteria for children were defined as age 4-12 years,
  • Having no known systemic disease,
  • visiting a dentist for the first time,
  • not having reported acute pain.

Exclusion criteria

Exclusion Criteria:

  • The exclusion criteria for children were defined as having systemic disease,
  • Having reported acute pain.
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
280 participants (actual)
Patient registry
No

Groups and cohorts

  • anxious group

    Children with a score ≥4 on the venham picture test were included.

    Behavioral: dental anxiety and oral hygiene

  • non-anxious group

    Children with a score \<4 on the venham picture test were included.

Interventions

  • Behavioraldental anxiety and oral hygiene

    Evaluation of the effect of mothers' dental anxiety and oral hygiene on children's dental anxiety and periodontal status.

06

What researchers measure

Primary outcomes

  1. Evaluation of the child's dental anxiety level

    The Venham Picture Test (VPT) was applied to the children to determine dental anxiety levels. The VPT consists of eight illustrations of human figures expressing various emotional reactions. The child selects pictures to reflect their current emotions. Each picture of an anxious child is assigned a score of 1, and each picture of a non-anxious child is assigned a score of 0. The total score ranges from 0 to 8, with a high score indicating a high level of anxiety, and a score of ≥4 is evaluated as high level dental anxiety. The children were separated into two groups based on whether or not they were classified as anxious.

    Time frame: 2 years

Secondary outcomes

  1. Evaluation of the mother's dental anxiety level

    Modified Dental Anxiety Scale (MDAS) was applied to the mothers to determine dental anxiety levels. The MDAS consists of 5 items providing a total score ranging from 5 to 25 points. A MDAS score ≥19 is evaluated as a high level of dental anxiety.

    Time frame: 2 years

07

Study locations

1 site
  • Okan university
    İstanbul, Tuzla 34947, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 3, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05563532
Lead sponsor
Okan University
Responsible party
Ekin Besiroglu (assistant profesor, Okan University) — Principal investigator
First posted
Oct 3, 2022
Start date
Dec 1, 2019
Primary completion
Apr 1, 2022
Completion
Sep 1, 2022
Last update
Oct 3, 2022

Oversight

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

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