- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05890040
Evaluation of the Effect of Watching Surgery Videos on Social Media on Anxiety Before Impacted Wisdom Tooth Extraction
May 24, 2023 updated by: Berkan Altay, DDS, Kutahya Health Sciences University
Surgical extraction of impacted wisdom teeth creates a high level of anxiety on patients.
Anxiety in patients can affect the difficulty of tooth extraction, prolong the duration of surgery and increase post-operative pain.
With the increasing internet usage in recent years; patients can access different information about surgical procedures by watching videos on various social media platforms in an uncontrolled manner.
In the literature, the effects of impacted tooth extraction videos, which are watched by physicians before the operation, on anxiety have been examined.
However, studies on the evaluation of the effect of the surgery videos watched by the patients before the surgery on their own will on anxiety and pain perception have been limited.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
The study is given to KSBU Faculty of Dentistry, Department of Oral, Dental and Maxillofacial Surgery; It will be applied to patients who are referred from Oral, Dental and Maxillofacial Radiology and who want to participate in the study.
In our study, the Situational-Trait Anxiety Inventory will be used to assess anxiety.
Patients who are referred to our clinic from Oral, Dental and Maxillofacial Radiology and who have impacted wisdom teeth will be evaluated in terms of extraction indication.
Patients with indications for extraction will be asked to rate the sentences in the State and Trait Anxiety Inventory when making an appointment.
Patients will be informed about impacted tooth extraction as it is routinely practiced.
Within the scope of this study, no information about the extraction will be given in the Oral, Dental and Maxillofacial Radiology clinic, standard information will be given to the patients in our clinic and the surgery appointment will be given one week later.
On the day of tooth extraction, patients will be asked whether they watched a video about impacted tooth extraction from any social media platform.
The patients who watch the video will be assigned to the study group, and the patients who do not watch the video will be assigned to the control group, so the study will be conducted over two groups.
If the patient has watched the video; He will be asked whether he watches an animation video or a video with real surgery footage, and the reason for watching the video.
Then, before starting the operation, they will be asked to score the sentences in the Situational and Trait Anxiety Inventory.
By comparing the Situational Anxiety Inventory made at the time of the surgery appointment with the Situational Anxiety Inventory scores made just before the surgery, it will be evaluated whether the patients who watch videos have more anxiety.
At the same time, it will be evaluated whether the patients who have a high Trait Anxiety Inventory score when making an appointment and who generally have high anxiety watch more videos.
This study is planned to be performed on a total of 60 patients, 30 of whom watch videos and 30 who do not.
Study Type
Observational
Enrollment (Actual)
60
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Merkez
-
Kütahya, Merkez, Turkey
- Kütahya University of Health Sciences
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Patients between the ages of 18-45 who want to have their impacted tooth extracted
Description
Inclusion Criteria:
- Patients between the ages of 18-45
- The patient does not have any systemic disease.
- Patients with mesio-angular or 2 or 3 / B according to the Pell and Gregory classification of the impacted tooth radiographic grade according to Winter classification
Exclusion Criteria:
- Patients using antidepressant and anxiolytic drugs
- Patients with a history of impacted tooth extraction/difficult tooth extraction
- Patients with systemic disease
- Female patients who are pregnant or breastfeeding
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
patients watching surgery video
Situational and trait anxiety test will be applied to patients.
|
assessment of anxiety
|
|
patients who did not watch the surgery video
Situational and trait anxiety test will be applied to patients.
|
assessment of anxiety
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluation of anxiety in impacted wisdom tooth extraction
Time Frame: one week before impacted tooth extraction
|
State and trait anxiety inventory( STAI-T and STAI-S)
|
one week before impacted tooth extraction
|
|
Evaluation of anxiety in impacted wisdom tooth extraction
Time Frame: just before impacted tooth extraction
|
State and trait anxiety inventory( STAI-T and STAI-S)
|
just before impacted tooth extraction
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Berkan Altay, DDS, 05356557441
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 8, 2021
Primary Completion (Actual)
July 8, 2022
Study Completion (Estimated)
July 8, 2023
Study Registration Dates
First Submitted
March 28, 2023
First Submitted That Met QC Criteria
May 24, 2023
First Posted (Actual)
June 6, 2023
Study Record Updates
Last Update Posted (Actual)
June 6, 2023
Last Update Submitted That Met QC Criteria
May 24, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 021/12-08
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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