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Clinical Trials/NCT05720897
NCT05720897
Completed
Not Applicable

Comparing Brief Relaxation Period to Virtual Reality Period in Reducing Dental Anxiety Prior to Root Canal Treatment; a Randomized Control Trial

Indiana University1 site in 1 country60 target enrollmentJanuary 11, 2023
ConditionsDental Anxiety

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dental Anxiety
Sponsor
Indiana University
Enrollment
60
Locations
1
Primary Endpoint
State-Trait Anxiety Inventory State Sub-scale (STAI-S) Score at the End of the Appointment
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The goal of this study is to evaluate non-drug approaches to reducing dental anxiety prior to non-surgical root canal treatment. This will be done by comparing two relaxation methods which will be performed immediately prior to scheduled, clinical non-surgical root canal treatment. Measures of anxiety will be evaluated prior to, and after, the relaxation intervention, as well as after the non-surgical root canal treatment is completed. Participation in the study is completed in a single study visit.

Detailed Description

Fifty-eight participants who needed non-surgical root canal treatment were randomly assigned into 2 groups of ABR and VRR. One group received earphones to listen to a guided brief relaxation recording, focusing on a body scan of tense points with diaphragmatic breathing. The other group received Meta 2 virtual reality headsets to listen and watch a 360 inclusive and integrative experience of ambient music, high resolution graphic illustrations and immersive scenery. Participants self-reported levels of anxiety were assessed prior to and post treatment by conducting evaluations using the State Trait Anxiety Indicator (STAI-State \& Trait) and the use of both a self-reported Visual Analog Scale (VAS) as well as by assessing objective secondary biometrics of anxiety of heart rate (HR) and Blood Pressure (BP) pre intervention, post intervention and following treatment completion.

Registry
clinicaltrials.gov
Start Date
January 11, 2023
End Date
April 3, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Stuart Schrader

Clinical Associate Professor

Indiana University

Eligibility Criteria

Inclusion Criteria

  • requires non-surgical root canal treatment
  • is able to independently provide informed consent for root canal treatment
  • proficient in English

Exclusion Criteria

  • history of vertigo or severe motion sickness
  • history of severe psychiatric disease
  • history of seizures, concussions, or severe neurological conditions
  • visual or hearing impairments
  • cardiac pacemaker or defibrillator
  • will require nitrous oxide sedation, nor pharmacologic anxiolytics or sedatives for dental treatment

Outcomes

Primary Outcomes

State-Trait Anxiety Inventory State Sub-scale (STAI-S) Score at the End of the Appointment

Time Frame: End of the appointment, approximately 90+ minutes after baseline

STAI-S is a 20 item sub-scale questionnaire which measures subjective self-reported feelings of state anxiety. Responses for each item include four possible responses that range from "very much" to "not at all" and which correlate to a numerical value. Scores range from 20 to 80. A score of 45-80 indicates "high anxiety": 38-44 indicate "moderate anxiety": 20-37 indicate low or no anxiety.

Visual Analog Score (VAS) at the End of the Appointment

Time Frame: End of the appointment, approximately 90+ minutes after baseline

The VAS will be a single question in which the participant is asked to assign and report a numerical value to the amount of anxiety one is feeling in the moment. It consists of a 10 point scale, with one symbolizing no anxiety and 10 symbolizing unbearable anxiety.

Systolic Blood Pressure (SBP) at the End of the Appointment

Time Frame: End of the appointment, approximately 90+ minutes after baseline

BP will be measured three times during the single study visit: at enrollment (prior to the assigned relaxation intervention), at the end of the assigned relaxation intervention, and at the end of the appointment.

Diastolic Blood Pressure (DBP) at the End of the Appointment

Time Frame: End of the appointment, approximately 90+ minutes after baseline

BP will be measured three times during the single study visit: at enrollment (prior to the assigned relaxation intervention), at the end of the assigned relaxation intervention, and at the end of the appointment.

Heart Rate (HR) at the End of the Appointment

Time Frame: End of the appointment, approximately 90+ minutes after baseline

HR will be measured three times during the single study visit: at enrollment (prior to the assigned relaxation intervention), at the end of the assigned relaxation intervention, and at the end of the appointment.

State-Trait Anxiety Inventory Trait Sub-scale (STAI-T) Score at the End of the Appointment

Time Frame: End of the appointment, approximately 90+ minutes after baseline

STAI-T is a 20 item sub-scale questionnaire which measures subjective self-reported feelings of trait anxiety. Responses for each item include four possible responses that range from "not at all" to "very much" and which correlate to a numerical value. Scores range from 20 to 80. A score of 45-80 indicates "high anxiety": 38-44 indicate "moderate anxiety": 20-37 indicate low or no anxiety.

Study Sites (1)

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