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Tell-Show-Do for Reducing Dental Anxiety During Local Anesthesia

30 de mayo de 2026 actualizado por: Mustafa Sarp Kaya, Bezmialem Vakif University

Effect of the Tell-Show-Do Technique on Dental Anxiety During Local Anesthesia Administration in School-Aged Children

Dental anxiety is common in children and may increase during local anesthesia administration. Dental injection anxiety is one of the most frequently reported causes of dental anxiety in pediatric dental patients. Communication-based behavior guidance techniques are commonly used to reduce anxiety during dental procedures. Among these techniques, tell-show-do is widely used in pediatric dentistry and is generally accepted by parents.

This completed interventional study evaluated the effect of introducing the syringe and related injection equipment using the tell-show-do technique on dental anxiety during local anesthesia administration in school-aged children. Children aged 5 to 7 years who required dental treatment under buccal infiltration local anesthesia and had no previous dental treatment experience involving injection were enrolled after parental consent was obtained.

The study used a controlled within-subject design. Each child attended an adaptation appointment followed by two dental treatment appointments involving local anesthesia. The syringe and related equipment were introduced using the tell-show-do technique at one local anesthesia appointment, whereas the injection equipment was kept out of the child's field of vision at the other local anesthesia appointment. The order of exposure to the tell-show-do intervention differed between sequence groups.

Dental anxiety, behavior, and pain-related responses were assessed using validated scales, including the Facial Image Scale, Human Figure Drawing scale, Frankl Behavior Scale, Modified Frankl Behavior Scale, and Sound-Eye-Motor scale. Parent-reported child dental fear and parental dental anxiety were also recorded.

Descripción general del estudio

Descripción detallada

This completed interventional study was designed to evaluate the effect of the tell-show-do behavior guidance technique on dental anxiety during local anesthesia administration in school-aged children. The behavioral intervention consisted of introducing the syringe and related injection equipment to the child before local anesthesia administration using the tell-show-do technique.

Eligible participants were children aged 5 to 7 years who presented to the faculty pediatric dentistry clinic and required dental treatment involving buccal infiltration local anesthesia. Children were included if no previous dental treatment involving injection had been performed, no urgent dental treatment was required, and no special health care needs were present. Participation was based on parental informed consent.

The study followed a controlled within-subject interventional design with two exposure conditions. Each participant attended an initial adaptation appointment followed by two treatment appointments involving local anesthesia. During the adaptation appointment, a preventive dental procedure not requiring injection, such as fissure sealant application, fluoride application, or prophylaxis, was performed to familiarize the child with the dental setting.

At the end of the adaptation appointment, baseline trait dental anxiety was assessed using the Human Figure Drawing scale after the child was asked to draw a child receiving dental treatment in a clinic. Parent-reported child dental fear was assessed using the Children's Fear Survey Schedule-Dental Subscale. Parental dental anxiety was assessed using the Modified Dental Anxiety Scale and the Dental Anxiety Inventory Short Form. The child's behavior during dental treatment was evaluated using the Frankl Behavior Scale.

Participants were assigned to one of two intervention sequences. In one sequence, the tell-show-do intervention was applied during the second appointment, and the hidden-instrument condition was applied during the third appointment. In the other sequence, the hidden-instrument condition was applied during the second appointment, and the tell-show-do intervention was applied during the third appointment. In this design, each child served as an internal control.

During the tell-show-do condition, the syringe and related injection equipment were introduced before local anesthesia administration. The syringe and needle were assembled in front of the child, and the syringe was described in child-appropriate language, such as a hollow tube. Local anesthesia was then administered after the introduction of the equipment.

During the hidden-instrument condition, the syringe and related equipment were kept outside the child's field of vision before and during local anesthesia administration. The injection was performed with the child's eyes closed, and the equipment was not introduced before the procedure.

State dental anxiety after local anesthesia administration was assessed using the Facial Image Scale, which includes five facial images representing different emotional states. At the end of the second and third appointments, trait dental anxiety was reassessed using the Human Figure Drawing scale. Child behavior during local anesthesia administration was evaluated using the Modified Frankl Behavior Scale. Pain-related responses before, during, and after injection were assessed from video recordings using the Sound-Eye-Motor scale by an independent rater.

Statistical analysis included Spearman correlation analysis, independent samples t-test, and Mann-Whitney U test, as appropriate. Statistical significance was set at p < 0.05.

Tipo de estudio

Intervencionista

Inscripción (Actual)

59

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Istanbul
      • Istanbul, Istanbul, Turquía (Türkiye)
        • Bezmialem Vakif University Faculty of Dentistry Department of PEdiatric Dentistry

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Niño

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion Criteria:

  • Children requiring dental treatment under buccal infiltration local anesthesia

Exclusion Criteria:

  • Children whose parents/legal guardians refuse to sign the informed consent form
  • Children whose parents/legal guardians do not consent to the demonstration of the dental injector
  • Children requiring emergency treatment
  • Children with special healthcare needs
  • Children with a history of previous dental treatment performed under local anesthesia via injection

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Diagnóstico
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Early Tell-Show-Do Dental Injector Demonstration Sequence
Participants in this arm received the tell-show-do dental injector demonstration at the first injection-related visit. At the subsequent injection-related visit, the dental injector and related equipment were kept outside the child's field of vision before and during local anesthesia administration.
This behavioral intervention sequence consisted of introducing the dental injector and related equipment using the tell-show-do technique before local anesthesia administration at the first injection-related visit. At the subsequent injection-related visit, the dental injector and related equipment were kept outside the child's field of vision before and during local anesthesia administration.
Comparador activo: Delayed Tell-Show-Do Dental Injector Demonstration Sequence
Participants in this arm first received local anesthesia with the dental injector and related equipment kept outside the child's field of vision. At the subsequent injection-related visit, the dental injector and related equipment were introduced using the tell-show-do technique before local anesthesia administration.
This behavioral intervention sequence consisted of local anesthesia administration with the dental injector and related equipment kept outside the child's field of vision at the first injection-related visit. At the subsequent injection-related visit, the dental injector and related equipment were introduced using the tell-show-do technique before local anesthesia administration.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
State Dental Anxiety Assessed by the Facial Image Scale
Periodo de tiempo: Immediately after local anesthesia administration at each injection-related visit, over the 3-month study period.
State dental anxiety after local anesthesia administration was assessed using the Facial Image Scale. The Facial Image Scale is a self-report scale consisting of five faces ranging from very happy to very unhappy. Scores range from 1 to 5, with higher scores indicating greater state dental anxiety.
Immediately after local anesthesia administration at each injection-related visit, over the 3-month study period.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Child Cooperation Assessed by the Modified Frankl Behavior Scale
Periodo de tiempo: During local anesthesia administration at each injection-related visit, over the 3-month study period.
Child cooperation during local anesthesia administration was assessed using the Modified Frankl Behavior Scale. Scores range from 1 to 4, with higher scores indicating more positive behavior and better cooperation.
During local anesthesia administration at each injection-related visit, over the 3-month study period.
Pain-Related Response Assessed by the Sound-Eye-Motor Scale
Periodo de tiempo: Before, during, and after local anesthesia administration at each injection-related visit, over the 3-month study period.
Pain-related behavioral response before, during, and after local anesthesia administration was assessed from video recordings using the Sound-Eye-Motor scale. The Sound-Eye-Motor scale evaluates sound, eye, and motor responses. Total scores range from 3 to 12, with higher scores indicating greater pain-related behavior or discomfort.
Before, during, and after local anesthesia administration at each injection-related visit, over the 3-month study period.
Parent-Reported Child Dental Fear Assessed by the Children's Fear Survey Schedule-Dental Subscale
Periodo de tiempo: At the adaptation appointment before the injection-related visits.
Parent-reported child dental fear was assessed using the Children's Fear Survey Schedule-Dental Subscale. The scale consists of 15 items scored on a 5-point Likert scale. Total scores range from 15 to 75, with higher scores indicating greater dental fear.
At the adaptation appointment before the injection-related visits.
Trait Dental Anxiety Assessed by the Human Figure Drawing Scale
Periodo de tiempo: At the adaptation appointment and at the end of each injection-related visit, over the 3-month study period.
Trait dental anxiety was assessed using the Human Figure Drawing scale. The scale was scored according to the study scoring system, with total scores ranging from 15 to 290. Higher scores indicate greater trait dental anxiety.
At the adaptation appointment and at the end of each injection-related visit, over the 3-month study period.
Child Behavior Assessed by the Frankl Behavior Rating Scale
Periodo de tiempo: During the adaptation appointment before the injection-related visits.
Child behavior during the adaptation appointment was assessed using the Frankl Behavior Rating Scale. Scores range from 1 to 4, with higher scores indicating more positive behavior and better cooperation.
During the adaptation appointment before the injection-related visits.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Director de estudio: Mustafa Sarp Kaya, DDS, PhD, Bezmialem Vakif University Department of Pediatric Dentistry

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de septiembre de 2022

Finalización primaria (Actual)

28 de noviembre de 2022

Finalización del estudio (Actual)

15 de mayo de 2023

Fechas de registro del estudio

Enviado por primera vez

23 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

30 de mayo de 2026

Publicado por primera vez (Actual)

4 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

4 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

30 de mayo de 2026

Última verificación

1 de marzo de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 2011-KAEK-42

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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