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Virtual Reality and Point-of-View Video Modeling for Dental Anxiety in Children

4 listopada 2026 zaktualizowane przez: Didem ATABEK

Comparison of "Virtual Reality" (VR) and "Point-of-View" (POV) Video Modeling Techniques for Reducing Dental Anxiety in Children

Dental anxiety is common among children and may make dental treatment more difficult. This study aims to compare three non-pharmacological behavior guidance techniques for reducing dental anxiety and improving cooperation during invasive fissure sealant treatment in children aged 6-10 years.

Children who require an invasive fissure sealant on a mandibular first molar and meet the study eligibility criteria will be included. Participants will be randomly assigned to one of three groups. The first group will watch a 1.5-2-minute Point-of-View (POV) video showing the dental examination and treatment process from a child's perspective before the dental procedure. The second group will use virtual reality (VR) glasses during the procedure and watch age-appropriate animation or cartoon content as an active distraction technique. The control group will receive the standard Tell-Show-Do behavior guidance technique.

Dental anxiety, behavior, physiological responses, and pain will be assessed using the Children's Fear Survey Schedule-Dental Subscale (CFSS-DS), Facial Image Scale (FIS), Frankl Behavior Rating Scale, pulse rate, oxygen saturation, and Wong-Baker FACES Pain Rating Scale. A post-intervention satisfaction and experience questionnaire will also be administered to assess the children's experiences with the behavior guidance techniques.

The study is expected to provide comparative evidence regarding the effectiveness of POV video modeling and VR distraction compared with the standard Tell-Show-Do technique in managing dental anxiety and improving children's cooperation during dental treatment.

Przegląd badań

Status

Rekrutacyjny

Warunki

Interwencja / Leczenie

Szczegółowy opis

The Facial Image Scale (FIS) will be used to evaluate the child's anxiety at four predefined time points: while the child is waiting in the waiting area, after sitting in the dental unit before the behavior guidance technique, after application of the assigned behavior guidance technique, and after completion of the invasive fissure sealant procedure.

Pulse rate and oxygen saturation will also be recorded at the same four assessment time points using a pulse oximeter. The Frankl Behavior Rating Scale will be used to assess behavioral cooperation before and during the dental procedure. Immediately after completion of the invasive fissure sealant procedure, pain will be assessed using the Wong-Baker FACES Pain Rating Scale. A post-intervention satisfaction and experience questionnaire will also be administered to evaluate the child's experience and perceived comfort with the assigned behavior guidance technique.

Typ studiów

Interwencyjne

Zapisy (Szacowany)

69

Faza

  • Nie dotyczy

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Kopia zapasowa kontaktu do badania

Lokalizacje studiów

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

6 lat do 10 lat (Dziecko)

Akceptuje zdrowych ochotników

Tak

Płeć kwalifikująca się do nauki

Wszystko

Opis

Inclusion Criteria:

  • Children aged 6-10 years.
  • Children without any systemic or psychiatric disorder or special needs.
  • Children who do not require emergency dental treatment.
  • Children whose parent(s) provide written and/or verbal informed consent for participation in the study.
  • Children who agree to participate in the assigned intervention, including watching the POV video or using virtual reality (VR) glasses, as applicable.

Exclusion Criteria:

  • Children with a systemic or psychiatric disorder or special needs.
  • Children who require emergency dental treatment.
  • Children who refuse to use virtual reality (VR) glasses.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Inny
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: POV Video Modeling Group

Participants in this group will watch a 1.5-2-minute Point-of-View (POV) video before the dental procedure. The video presents the dental examination and treatment process from a child's perspective and is designed to familiarize the child with the dental procedure before invasive fissure sealant treatment.

Participants will watch a 1.5-2-minute Point-of-View (POV) video before the dental procedure. The video presents the dental examination and treatment process from a child's perspective and is intended to familiarize the child with the dental procedure before invasive fissure sealant treatment.

Eksperymentalny: Virtual Reality (VR) Group

Participants in this group will use virtual reality (VR) glasses during the dental procedure. Age-appropriate animation or cartoon content will be presented through the VR glasses as an active distraction technique during invasive fissure sealant treatment.

Participants will use virtual reality (VR) glasses during the dental procedure. Age-appropriate animation or cartoon content will be presented through the VR glasses as an active distraction technique during invasive fissure sealant treatment.

Aktywny komparator: Tell-Show-Do Control Group

Participants in this group will receive the standard Tell-Show-Do behavior guidance technique before and during the invasive fissure sealant procedure. The child will be introduced to the dental procedure using the standard Tell-Show-Do approach.

Participants in the control group will receive the standard Tell-Show-Do behavior guidance technique before and during the invasive fissure sealant procedure. The child will be introduced to the dental procedure using the standard Tell-Show-Do approach.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Facial Image Scale (FIS) Score
Ramy czasowe: Visit 1: Within 1 min after dental examination. Visit 2 (2 weeks later): (1) Before dental examination; (2) within 1 min after seating; (3) within 1 min after behavior guidance; (4) within 1 min after fissure sealant.

The Facial Image Scale (FIS) is a self-report measure used to assess dental anxiety in children. It consists of five facial images representing increasing levels of anxiety, scored from 1 to 5. A score of 1 indicates the least anxiety, whereas a score of 5 indicates the highest anxiety. Higher scores indicate greater dental anxiety and therefore a worse outcome.

FIS scores will be recorded at five time points. During the first visit, the FIS will be administered within 1 minute after completion of the dental examination. During the second visit, which will take place 2 weeks after the initial visit, FIS scores will be recorded at four time points: (1) in the waiting area immediately before the dental examination; (2) within 1 minute after the child is seated in the dental chair; (3) within 1 minute after completion of the assigned behavior guidance technique and before dental treatment; and (4) within 1 minute after completion of the invasive fissure sealant procedure.

Visit 1: Within 1 min after dental examination. Visit 2 (2 weeks later): (1) Before dental examination; (2) within 1 min after seating; (3) within 1 min after behavior guidance; (4) within 1 min after fissure sealant.

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Children's Fear Survey Schedule-Dental Subscale (CFSS-DS) Score
Ramy czasowe: Visit 1: Within 5 min after dental examination. Visit 2 (2 weeks later): Within 5 min after fissure sealant procedure.

Dental fear and anxiety will be assessed using the Children's Fear Survey Schedule-Dental Subscale (CFSS-DS), a 15-item scale scored from 15 to 75. Higher scores indicate greater dental fear and anxiety and a worse outcome. Scores are categorized as low (≤32), moderate (33-37), and high (≥38) dental anxiety. CFSS-DS scores will be recorded within 5 minutes after completion of the dental examination during the first visit and within 5 minutes after completion of the fissure sealant procedure during the second visit, which will take place 2 weeks after the initial visit.

Visit 1: Within 5 min after dental examination. Visit 2 (2 weeks later): Within 5 min after fissure sealant procedure.
Frankl Behavior Rating Scale Score
Ramy czasowe: Visit 1: During the dental examination. Visit 2: Before the behavior guidance technique: during the dental examination; after the behavior guidance technique: Throughout the fissure sealant procedure, including at treatment completion.

The child's behavior will be assessed using the Frankl Behavior Rating Scale, which consists of four categories scored from 1 to 4: definitely negative (1), negative (2), positive (3), and definitely positive (4). Higher scores indicate more positive behavior and a better outcome.The child's behavior will be observed during the dental examination at the first visit and, at the second visit, during the dental examination before the behavior guidance technique and throughout the fissure sealant procedure, including at treatment completion. The second visit will take place 2 weeks after the initial visit.

Visit 1: During the dental examination. Visit 2: Before the behavior guidance technique: during the dental examination; after the behavior guidance technique: Throughout the fissure sealant procedure, including at treatment completion.
Pulse Rate
Ramy czasowe: Visit 2: (1) In the waiting area, before dental examination; (2) within 1 min after seating in dental unit; (3) within 1 min after behavior guidance, before dental treatment; (4) within 1 min after fissure sealant.

Pulse rate (beats per minute, bpm) will be measured at four time points during the second visit: (1) in the waiting area immediately before the dental examination; (2) within 1 minute after the child is seated in the dental chair; (3) within 1 minute after completion of the assigned behavior guidance technique and before dental treatment; and (4) within 1 minute after completion of the invasive fissure sealant procedure.

Visit 2: (1) In the waiting area, before dental examination; (2) within 1 min after seating in dental unit; (3) within 1 min after behavior guidance, before dental treatment; (4) within 1 min after fissure sealant.
Oxygen Saturation (SpO2)
Ramy czasowe: Visit 2: (1) In the waiting area, before dental examination; (2) within 1 min after seating in dental unit; (3) within 1 min after behavior guidance, before dental treatment; (4) within 1 min after fissure sealant.

Oxygen saturation (SpO₂), expressed as a percentage (%), will be measured at four time points during the second visit: (1) in the waiting area immediately before the dental examination; (2) within 1 minute after the child is seated in the dental chair; (3) within 1 minute after completion of the assigned behavior guidance technique and before dental treatment; and (4) within 1 minute after completion of the invasive fissure sealant procedure. Changes in SpO₂ will be evaluated across these time points.

Visit 2: (1) In the waiting area, before dental examination; (2) within 1 min after seating in dental unit; (3) within 1 min after behavior guidance, before dental treatment; (4) within 1 min after fissure sealant.
Wong-Baker FACES Pain Rating Scale Score
Ramy czasowe: Visit 2: Within 1 min after completion of the fissure sealant procedure.

Pain intensity will be assessed using the Wong-Baker FACES Pain Rating Scale, scored from 0 to 10 in increments of 2 (0, 2, 4, 6, 8, and 10). A score of 0 indicates no pain, while 10 indicates the worst pain. Higher scores indicate greater pain intensity and a worse outcome. Pain will be assessed within 1 minute after completion of the invasive fissure sealant procedure during the second visit.

Visit 2: Within 1 min after completion of the fissure sealant procedure.
Satisfaction and Experience Questionnaire
Ramy czasowe: Visit 2: Within 5 min after completion of the fissure sealant procedure (POV and VR groups only).

A post-intervention Satisfaction and Experience Questionnaire will be administered to participants in the POV Video Modeling and Virtual Reality (VR) groups within 5 minutes after completion of the fissure sealant procedure to assess their satisfaction, perceptions, and comfort regarding the assigned behavior guidance technique. Items will be answered with "Yes" or "No."

Visit 2: Within 5 min after completion of the fissure sealant procedure (POV and VR groups only).

Współpracownicy i badacze

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Sponsor

Współpracownicy

Śledczy

  • Główny śledczy: Didem Atabek, Prof. Dr., Gazi University

Publikacje i pomocne linki

Osoba odpowiedzialna za wprowadzenie informacji o badaniu dobrowolnie udostępnia te publikacje. Mogą one dotyczyć wszystkiego, co jest związane z badaniem.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

20 października 2026

Zakończenie podstawowe (Szacowany)

1 stycznia 2027

Ukończenie studiów (Szacowany)

1 stycznia 2027

Daty rejestracji na studia

Pierwszy przesłany

19 października 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

19 października 2026

Pierwszy wysłany (Rzeczywisty)

26 października 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

9 listopada 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

4 listopada 2026

Ostatnia weryfikacja

1 listopada 2026

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • 2025-2098

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .