Evaluation of The Effect of Consecutive Dental Visits on Dental Anxiety of Paediatric Patients

February 12, 2024 updated by: Hamit Tunc, Burdur Mehmet Akif Ersoy University

The goal of this observational study is to learn about in effect of consecutive dental visits on dental anxiety of paediatric patients.

The main question[s]it aims to answer are:

  • Did the anxiety level of pediatric patients decrease in consecutive treatment sessions?
  • Were there changes in the physiological parameters related to stress level of pediatric patients in consecutive treatment sessions?

Participants will fill out the questionnaire about dental anxiety in each dental treatment sessions before and after dental treatment.

Researchers will compare paeditric patients have two caries on mandibular molars to see if changes dental anxiety levels and physiological parameters such as heart rates and oxygen saturations during dental treatments in consecutive dental treatment sessions.

Study Overview

Detailed Description

The aim of this study was to investigate the effect of consecutive dental visits on paediatric patients' dental anxiety level in 6-9 years old Turkish children with using of Abeer Children Dental Anxiety scale and physiological parameters.

Determination of Sample Size and Study Design The significance level for the sample size in the study was regulated to show an effect size of 0.83 with a power of 0.05 and 95%. The number of samples (n) was calculated as 200. However, it was decided that the total number of samples (n) would be 260 with data loss foreseen.

According to American Society of Anaesthesiologists (ASA), ASA1 and ASA2 healthy children who 6-9 years old without any learning and physical disabilities, children who don't need to emergency dental applications, children who can speak and understand Turkish, children who have dental caries that involved only dentine and enamel and were included to this study. Children with any disabilities that physical and mental or without parental consent were excluded from this study. In addition to this, children who has a systemic disease with changing the blood pressure, oxygen saturation and heart rate were excluded from this study. 260 children who met the inclusion criteria invited to the study.

Collection of Data and Study Procedure The ACDAS that including three parts as evaluation of child, dental, cognitive and 19 questions was used as a cognitive scale for this study. In the dental part of ACDAS including 13 questions, the children answered these questions using with three types of facial expressions for to show how they felt. All the answers were scored with scale of 1-3. According to the ACDAS children who have score of 26 and above were classified as anxious. The child evaluation and cognitive parts of ACDAS were answered by the paediatric dentist and child's legal guardians. The scores of ACDAS were accepted for master scores. Children were examined by the paediatric dentist as only clinical and radiographical without any dental treatment on first visit.

All participants were recorded, and their appointments were made by the dental assistant. Children were treated with topical anaesthesia (cotton with lidocaine %10 spray) followed by buccal infiltration local anaesthesia (articaine hydrochloride %4) for caries removing of one of the primary molars. The two mandibular primary molars of children were restored with compomer resin with using the rubber dam in first and second visits. All children were directed by same paediatric dentist (HT) with non-pharmacological behaviour management techniques during the dental treatments such as tell-show-do.The treatment duration was approximately 15 minutes. All participants completed to ACDAS for the two times as pre and post operative in both visits.

The objective symptoms of evaluation of dental anxiety such as oxygen saturation and heart rate were included in this study. Heart rate and oxygen saturations of each patient were measured with pulse oximeter (PC-60FL Finger Type Pulse Oxymeter, Galena, TURKEY). The heart rate and oxygen saturation were measured in 5th, 10 th and 15th minutes in first and second visits during dental procedures.

Statistical Analysis All data were analysed with SPSS 22.0 (SPSS for Windows, SPSS Inc, Chicago, IL) and GraphPad Prism software 7.0 for Windows (GraphPad Software, San Diego, California, USA). The sample size of the study was calculated with G-Power (version 3.1.9.7, Heinrich-Heine-Universität Düsseldorf, Germany). Calculation of the normality of the data was using with Kolmorognov-Simirnov test and followed by parametric tests. All data showed normal distribution. Standard deviation (SD) and mean values were shown with numerical variables. Categorical variables were shown with percentages. Two sample t-test were performed for comparing the differences between mean ACDAS score and physiological parameters of first and second visits.

Study Type

Observational

Enrollment (Actual)

240

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Centrum
      • Burdur, Centrum, Turkey, 15100
        • Burdur Mehmet Akif Ersoy University Faculty of Dentistry

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

Probability Sample

Study Population

Children aged 6-9 years who meet the inclusion criteria and needed at least two restorative dental treatments of the mandibular first primary molar were included in the study.

Description

Inclusion Criteria:

  • According to American Society of Anaesthesiologists (ASA), ASA1 and ASA2 healthy children who 6-9 years old without any learning and physical disabilities, children who don't need to emergency dental applications, children who can speak and understand Turkish, children who have dental caries that involved only dentine and enamel and were included to this study.

Exclusion Criteria:

  • Children with any disabilities that physical and mental or without parental consent were excluded from this study. In addition to this, children who has a systemic disease with changing the blood pressure, oxygen saturation and heart rate were excluded from this study.

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Firts Dental Visit
Dental anxiety level, heart rate and oxygen saturation of participants in first dental visit.
All participants were answered the dental anxiety questionnaire.
All participants heart rate were measured with finger type pulse oxymeter.
All participants oxygen saturation were measured with finger type pulse oxymeter.
Second dental visit
Dental anxiety level, heart rate and oxygen saturation of participants in second dental visit.
All participants were answered the dental anxiety questionnaire.
All participants heart rate were measured with finger type pulse oxymeter.
All participants oxygen saturation were measured with finger type pulse oxymeter.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Determination of sample size.
Time Frame: Before the starting to study
The significance level for the sample size in the study was regulated to show an effect size of 0.83 with a power of 0.05 and 95%. The number of samples (n) was calculated as 200. However, it was decided that the total number of samples (n) would be 260 with data loss foreseen.
Before the starting to study
Inviting participants to the study.
Time Frame: Before the starting to study
ASA1 and ASA2 healthy children who 6-9 years old without any learning and physical disabilities, children who don't need to emergency dental applications, children who can speak and understand Turkish, children who have dental caries that involved only dentine and enamel and were included to this study. The Abeer Children Dental Anxiety Scale that including three parts as evaluation of child, dental, cognitive and 19 questions was used as a cognitive scale for this study. All the answers were scored with scale of 1-3. Children who have score of 26 and above were classified as anxious. Heart rate and oxygen saturations of each patient were measured with pulse oximeter.
Before the starting to study
Determination of dental anxiety score of participants before dental treatment in first dental session
Time Frame: Before the starting to dental treatment in first session.
All participants completed The Abeer Children Dental Anxiety Scale (ACDAS) before starting treatment.The ACDAS that including three parts as evaluation of child, dental, cognitive and 19 questions was used as a cognitive scale for this study. In the dental part of ACDAS including 13 questions, the children answered these questions using with three types of facial expressions for to show how they felt. All the answers were scored with scale of 1-3. The total scores were ranging between 13 and 39. Children who have score of 26 and above were classified as anxious.
Before the starting to dental treatment in first session.
Heart rate measuring in first dental session.
Time Frame: Measured at the 5th, 10th and 15th minutes of dental treatment.
The heart rate were measured in every 5 minutes during dental procedures. Total dental treatment time 15 minutes.
Measured at the 5th, 10th and 15th minutes of dental treatment.
Oxygen saturation measuring in first dental session.
Time Frame: Measured at the 5th, 10th and 15th minutes of dental treatment.
The oxygen saturation were measured in every 5 minutes during dental procedures. Total dental treatment time 15 minutes.
Measured at the 5th, 10th and 15th minutes of dental treatment.
Determination of dental anxiety score of participants after dental treatment in first dental session
Time Frame: After the dental treatment in first session.
All participants completed the dental anxiety questionnaire after treatment process.
After the dental treatment in first session.
Determination of dental anxiety score of participants before dental treatment in second dental session
Time Frame: Before the starting to dental treatment in second session.
All participants completed the dental anxiety questionnaire before starting treatment.
Before the starting to dental treatment in second session.
Heart rate measuring in second dental session.
Time Frame: Measured at the 5th, 10th and 15th minutes of dental treatment.
The heart rate were measured in every 5 minutes during dental procedures. Total dental treatment time 15 minutes.
Measured at the 5th, 10th and 15th minutes of dental treatment.
Oxygen saturation measuring in second dental session.
Time Frame: Measured at the 5th, 10th and 15th minutes of dental treatment.
The oxygen saturation were measured in every 5 minutes during dental procedures. Total dental treatment time 15 minutes.
Measured at the 5th, 10th and 15th minutes of dental treatment.
Determination of dental anxiety score of participants after dental treatment in second dental session
Time Frame: After the dental treatment in second session.
All participants completed the dental anxiety questionnaire after treatment process.
After the dental treatment in second session.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Hamit Tunç, Ph.D, Burdur Mehmet Akif Ersoy University Faculty of Dentistry Deparment of Paediatric Dentistry

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 (Actual)

August 5, 2023

Primary Completion (Actual)

November 3, 2023

Study Completion (Actual)

December 27, 2023

Study Registration Dates

First Submitted

February 5, 2024

First Submitted That Met QC Criteria

February 12, 2024

First Posted (Actual)

February 20, 2024

Study Record Updates

Last Update Posted (Actual)

February 20, 2024

Last Update Submitted That Met QC Criteria

February 12, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • BMU-HTUNC-01

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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