Anxiety, Anxiety State, Tooth Extraction Status Nos
Conditions
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.
Interventions
OTHERGreen color exposure
Patients will wear green colored glasses before and during the surgery.
OTHERRed color exposure
Patients will wear red colored glasses before and during the surgery.
OTHERBlue color exposure
Patients will wear blue colored glasses before and during the surgery.
OTHERcontrol
Patients will wear translucent glasses before and during the surgery.
Sponsors
Selcuk University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in the Anxiety Score | 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
| Measure | Time frame | Description |
|---|---|---|
| Change in the oxygen saturation | 1 minute after the participant sits the dental unit and 10 minutes after | Saturation measurement is done from the fingertip using a pulse oximeter one minute after the patient sits in the dental unit and after ten minutes. Changes in the scores are the secondary outcome of the study. The average value is above %90. |
| Change in the pulsation | 1 minute after the participant sits the dental unit and 10 minutes after | Pulsation was measured from the fingertip by a pulse oximeter one minute after the patient sat in the dental unit and after ten minutes. Changes in the scores are the secondary outcome of the study. The average value is between 65 and 75. |
| Intraoperative Pain Score | 1 minutes after the surgery | Measuring the pain felt by the patient after the operation with the help of the visual analog scale. The range of Scala is 0-10. A lower score means better results. |
| Change in the salivary cortisol level | 1 minute after the participant sits the dental unit and 10 minutes after | Measuring the salivary cortisol level one minute after the patient sits in the dental unit and after ten minutes. Changes in the levels are the secondary outcome of the study. |
| Change in the salivary alfa-amilase level | 1 minute after the participant sits the dental unit and 10 minutes after | Measuring the salivary alfa-amylase level one minute after the patient sits in the dental unit and after ten minutes. Changes in the levels are the secondary outcome of the study. |
Countries
Turkey (Türkiye)
Contacts
STUDY_CHAIRGökhan Gürses
Selcuk University, Faculty of Dentistry
PRINCIPAL_INVESTIGATORİsmail Okumuş
Selcuk University, Faculty of Medicine
Outcome results
None listed