- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07656948
The Effect of Teledentistry on Dental Anxiety in Children: A Randomized Clinical Trial
16 juni 2026 uppdaterad av: Venus Seyedoskuyi, Istanbul Aydın University
This randomized controlled trial aimed to evaluate the effect of a brief teledentistry consultation on dental anxiety in children aged 7-11 years.
Two hundred children with no previous dental visits or treatment experience were randomly assigned to either a teledentistry group or a conventional clinical examination group.
The teledentistry group received a standardized 3-5-minute pre-appointment video consultation via WhatsApp before their first dental visit.
Dental anxiety was assessed using subjective and physiological parameters before and after the examination.
The study investigated whether teledentistry could reduce dental anxiety and improve children's adaptation to their first dental visit.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
This randomized controlled trial was conducted at the Department of Pediatric Dentistry, Faculty of Dentistry, Istanbul Aydin University, Istanbul, Turkey.
The study included 200 children aged 7-11 years with no previous dental visits, dental treatment experience, or dental complaints.
Participants were randomly allocated to either a teledentistry group (n=100) or a conventional clinical examination group (n=100).
In the teledentistry group, children participated in a standardized synchronous 3-5-minute pre-appointment consultation via WhatsApp.
During the consultation, children were introduced to the dentist, dental instruments, oral health concepts, and the examination process.
The conventional group underwent direct face-to-face examination without prior virtual interaction.
Dental anxiety was assessed using the Facial Image Scale (FIS), heart rate, and oxygen saturation measured before and after clinical examination.
The primary outcome was the difference in post-examination FIS scores between groups.
Secondary outcomes included changes in heart rate and oxygen saturation.
Studietyp
Interventionell
Inskrivning (Faktisk)
200
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
Kucukcekmece
-
Istanbul, Kucukcekmece, Turkiet (Türkiye)
- Istanbul Aydin University
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Barn
Tar emot friska volontärer
Ja
Beskrivning
Inclusion Criteria:
- Children aged 7 to 11 years.
- Children attending their first dental examination appointment.
- Children requiring a non-emergency dental examination.
- Children and their parents/legal guardians who provided written informed consent.
Exclusion Criteria:
- Children with previous dental treatment experience.
- Children with systemic diseases, neurological disorders, or developmental disabilities that could affect anxiety assessment.
- Children requiring emergency dental treatment.
- Children whose parents/legal guardians did not provide consent.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Hälsovårdsforskning
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Teledentistry Group
Participants received a standardized 3-5-minute synchronous teledentistry consultation via WhatsApp before their first dental examination.
Children were introduced to the dentist, dental instruments, oral health concepts, and the examination process.
|
A standardized synchronous teledentistry consultation delivered via WhatsApp for 3-5 minutes before the first dental examination.
Children were introduced to the dentist, dental instruments, oral health concepts, and the examination process.
|
|
Aktiv komparator: Conventional Clinical Examination Group
Participants underwent a conventional face-to-face clinical examination without prior teledentistry consultation.
Children met the pediatric dentist for the first time during their scheduled dental appointment and received a routine clinical examination.
|
Participants underwent a routine face-to-face dental examination without prior teledentistry consultation.
Children attended their first dental visit and received a standard clinical examination performed by a pediatric dentist.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Subjective dental anxiety in children
Tidsram: Before and immediately after the first dental examination (same day)
|
Dental anxiety levels of children assessed before and after the first dental examination using the Facial Image Scale (FIS).
|
Before and immediately after the first dental examination (same day)
|
|
Objective dental anxiety assessed by oxygen saturation
Tidsram: Before and immediately after the first dental examination (same day)
|
Peripheral oxygen saturation (SpO2) was measured before and immediately after the first dental examination as an objective physiological parameter of dental anxiety.
|
Before and immediately after the first dental examination (same day)
|
|
Objective dental anxiety assessed by heart rate
Tidsram: Before and immediately after the first dental examination (same day)
|
Heart rate was measured before and immediately after the first dental examination as an objective physiological parameter of dental anxiety.
|
Before and immediately after the first dental examination (same day)
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
11 september 2023
Primärt slutförande (Faktisk)
23 juli 2024
Avslutad studie (Faktisk)
27 september 2024
Studieregistreringsdatum
Först inskickad
16 juni 2026
Först inskickad som uppfyllde QC-kriterierna
16 juni 2026
Första postat (Faktisk)
18 juni 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
18 juni 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
16 juni 2026
Senast verifierad
1 juni 2026
Mer information
Termer relaterade till denna studie
Nyckelord
Andra studie-ID-nummer
- 2022/143
Plan för individuella deltagardata (IPD)
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NEJ
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