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Clinical Trials/NCT06452836
NCT06452836
Completed
Not Applicable

Colors, Can They Reduce the Dental Anxiety

Selcuk University1 site in 1 country84 target enrollmentFebruary 1, 2024

Overview

Phase
Not Applicable
Intervention
Blue color exposure
Conditions
Anxiety
Sponsor
Selcuk University
Enrollment
84
Locations
1
Primary Endpoint
Change in the Anxiety Score
Status
Completed
Last Updated
10 days ago

Overview

Brief Summary

The investigator's aim in this study was to evaluate the preoperative anxiety and pain felt during the operation due to exposure to green, red, and blue light. For this purpose, the participants will wear colored glasses before the operation. The investigator will evaluate the patient's anxiety change and the pain she/he feels during the procedure.

Registry
clinicaltrials.gov
Start Date
February 1, 2024
End Date
December 1, 2025
Last Updated
10 days ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Gokhan Gurses

Assistant Professor

Selcuk University

Eligibility Criteria

Inclusion Criteria

  • ASA 1 and ASA 2 patient population
  • not having had a third molar surgery before
  • volunteer to participate in the study

Exclusion Criteria

  • dental phobia
  • patients who will be treated under general anesthesia
  • refusing the measurements
  • not filling out the VAS
  • encountering complications during surgery
  • operations lasting more than 45 minutes

Arms & Interventions

Blue Colored Glasses Group

Intervention: Blue color exposure

Translucent Glasses Group

Intervention: control

Green Colored Glasses Group

Intervention: Green color exposure

Red Colored Glasses Group

Intervention: Red color exposure

Outcomes

Primary Outcomes

Change in the Anxiety Score

Time Frame: 1 minute after the participant sits the dental unit and 10 minutes after

Patients complete the State-Trait Anxiety Inventory (STAI) while seated in the dental unit. Ten minutes after the glasses are worn, patients fill out the anxiety scale again. Changes in the scores are the primary outcome of the study. The scale range is 20-40. A lower score means better results.

Secondary Outcomes

  • Change in the salivary cortisol level(1 minute after the participant sits the dental unit and 10 minutes after)
  • Change in the oxygen saturation(1 minute after the participant sits the dental unit and 10 minutes after)
  • Change in the pulsation(1 minute after the participant sits the dental unit and 10 minutes after)
  • Intraoperative Pain Score(1 minutes after the surgery)
  • Change in the salivary alfa-amilase level(1 minute after the participant sits the dental unit and 10 minutes after)

Study Sites (1)

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