CClinicalTrials.gg
CompletedNCT07653854VR-IANBUpdated Jun 17, 2026

Virtual Reality Training for Inferior Alveolar Nerve Block in Dental Students

An interventional study of SIMtoCARE Virtual Reality Simulator and Conventional Training in Dental Education and Inferior Alveolar Nerve Block, sponsored by Konya Necmettin Erbakan Üniversitesi. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-17.

Sponsored by Konya Necmettin Erbakan Üniversitesi · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 10 months after the study started (first participant enrolled Aug 2025, registered Jun 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
132
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This randomized controlled study aims to evaluate the effectiveness of virtual reality simulator-based training in teaching the inferior alveolar nerve block (IANB) technique to third-year dental students. Participants were randomly assigned to either a virtual reality simulator training group or a conventional training group. The outcomes evaluated include theoretical knowledge, anatomical understanding, procedural performance, self-confidence, and anxiety levels associated with IANB administration. The study aims to determine whether virtual reality simulation provides advantages over conventional educational methods in local anesthesia training.

Read the detailed description

Inferior alveolar nerve block (IANB) is one of the most frequently performed local anesthesia techniques in dentistry and requires adequate theoretical knowledge, anatomical understanding, and psychomotor skills. Traditional educational methods may not provide sufficient opportunities for repeated practice without patient involvement.

Virtual reality (VR) simulators with haptic feedback have emerged as innovative educational tools that allow students to perform procedures in a safe and controlled environment. However, evidence regarding their effectiveness in IANB training remains limited.

This randomized controlled study evaluates the effectiveness of a VR simulator (SIMtoCARE) in teaching the IANB technique to third-year dental students at the Faculty of Dentistry, Necmettin Erbakan University. Participants were randomly assigned to either a VR-based training group or a conventional training group.

A total of three questionnaires were administered to the students. Based on the results of these questionnaires, several parameters, including theoretical knowledge, anatomical awareness, self-confidence, and anxiety levels, were evaluated.

The findings of this study may contribute to the development of evidence-based educational strategies and support the integration of VR simulation into the dental education curriculum.

02

Conditions studied

  • Dental Education
  • Inferior Alveolar Nerve Block

Keywords

  • Haptic Simulator
  • SIMtoCARE
  • Dental Education
  • Inferior Alveolar Nerve Block
  • Local Anesthesia
  • Dental Students
  • Simulation-Based Training
  • Randomized Controlled Trial
03

In context

Lead sponsor

Konya Necmettin Erbakan Üniversitesi is the lead sponsor of 27 studies on the registry; 4 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Being a third-year student at our Faculty of Dentistry Willingness to participate in the study voluntarily

Exclusion criteria

Exclusion Criteria:

  • Having previously received local anesthesia training using a virtual reality simulator Unwillingness to participate in the study
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
132 participants (actual)

Study arms

  • Experimental
    Virtual Reality Training Group

    Participants completed the first questionnaire after the theoretical training. They then received virtual reality simulator-based training using the SIMtoCARE system. Following this training, they completed the second questionnaire. After the virtual reality training, participants also received conventional training and completed the third questionnaire.

    Other: SIMtoCARE Virtual Reality Simulator · Other: Conventional Training

  • Active comparator
    Conventional Training Group

    Participants completed the first questionnaire after the theoretical training. They then received conventional training and completed the third questionnaire at the end of the training.

    Other: Conventional Training

Interventions

  • OtherSIMtoCARE Virtual Reality Simulator

    A haptic virtual reality simulator used for inferior alveolar nerve block training.

  • OtherConventional Training

    Traditional theoretical and practical instruction for inferior alveolar nerve block administration.

06

What researchers measure

Primary outcomes

  1. Change in inferior alveolar nerve block education questionnaire score

    Difference in questionnaire scores assessing theoretical knowledge, anatomical understanding, self-confidence, and anxiety related to inferior alveolar nerve block administration between baseline and post-training assessments. The effect of virtual reality simulator-based training will be evaluated through changes in these scores.

    Time frame: Baseline and immediately after completion of training

07

Study locations

1 site
  • Necmettin Erbakan Üniversitesi Diş Hekimliği Fakültesi
    Konya, 42090, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No — Individual participant data will not be shared with other researchers. The questionnaire data were collected anonymously and will be used only by the study investigators for research purposes.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 17, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07653854
Lead sponsor
Konya Necmettin Erbakan Üniversitesi
Responsible party
Kubilay Isik (Professor, Department of Oral and Maxillofacial Surgery, Konya Necmettin Erbakan Üniversitesi) — Principal investigator
First posted
Jun 17, 2026
Start date
Aug 1, 2025
Primary completion
May 22, 2026
Completion
May 22, 2026
Last update
Jun 17, 2026

Oversight

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

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This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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