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Clinical Trials/NCT06092177
NCT06092177
Completed
Not Applicable

Evaluation of Virtual Reality Distraction on Dental Anxiety in Patients Undergoing Periodontal Surgery

Kutahya Health Sciences University1 site in 1 country58 target enrollmentMay 2, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Virtual Reality
Sponsor
Kutahya Health Sciences University
Enrollment
58
Locations
1
Primary Endpoint
Anxiety level
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The goal of this randomized controlled clinical trial is to evaluate the effect of virtual reality technology on anxiety and pain levels in patients undergoing periodontal surgery.

Participants will be randomly assigned into test and control groups. While the patients in the test group will undergo periodontal surgery with virtual reality distraction, the patients in the control group without distraction. After treatment, the groups will be compared regarding anxiety and pain levels.

Registry
clinicaltrials.gov
Start Date
May 2, 2022
End Date
May 2, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Kutahya Health Sciences University
Responsible Party
Principal Investigator
Principal Investigator

Ezgi Gürbüz

Assistant Professor

Kutahya Health Sciences University

Eligibility Criteria

Inclusion Criteria

  • Individuals over the age of 18
  • Systemically healthy patients
  • Need for periodontal surgical treatment in the mandibular anterior region
  • Scoring 15 or above on the modified dental anxiety scale

Exclusion Criteria

  • Having a history of seizures or a convulsive disorder
  • Balance disorders such as nystagmus, vertigo
  • Use of psychotropic drugs
  • Getting treatment for anxiety
  • Presence of dermatological lesions on the face, especially around the eyes
  • A lesion in the eye that will prevent the use of virtual reality glasses
  • Systemic disease and medication use that contraindicate periodontal surgery

Outcomes

Primary Outcomes

Anxiety level

Time Frame: Preoperative, immediately postoperative

Modified dental anxiety scale where higher scores mean a worse outcome and has a minimum value of 5 and a maximum value of 25

Secondary Outcomes

  • Pain level(Preoperative, immediately postoperative)
  • Diastolic blood pressure(Preoperative, intraoperative, immediately postoperative)
  • Systolic blood pressure(Preoperative, intraoperative, immediately postoperative)
  • Heart rate(Preoperative, intraoperative, immediately postoperative)

Study Sites (1)

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