- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04453696
Dentist-Patient Communication on Dental Anxiety Using the Social Media and Timing in Communication
Dentist-Patient Communication on Dental Anxiety Using the Social Media and Timing in Communication: A Double-blinded Randomized Controlled Trial
Study Overview
Status
Detailed Description
The purpose of the present study was to assess the effects of dentist-patient communication via social media on dental anxiety, and second, to evaluate the appropriate timing of such communications.
Instagram's quick replies system was used to answer patients' questions to alleviate dental anxiety for patients undergoing impacted mandibular third-molar extraction under local anesthesia. Patients were assigned randomly into four groups according to timing of such communications: Communication before operation (n=36), Communication after operation (n=35), Communication before and after operation (n=36), and a control group who received no communication on social media (n=36). Dental anxiety was evaluated one week before and after the surgical operation using recognized assessment scales-the Spielberger's State-Trait Anxiety Inventory, Modified Dental Anxiety Scale and a visual analog scale.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Trabzon, Turkey, 61080
- Efe Can Sivrikaya
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Must be able to use the Instagram platform. I
- Clinicial diagnosis of mesioangular impacted lower third molar according to the classification of Winter and the Pell and Gregory classification (2 or 3/B).
Exclusion Criteria:
- Patients who previously obtained information from social media
- Bad dental history
- Systemic disease
- Pregnant
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Communication before operation
Communication was established before the operation.
|
STAI-S, like kinetic energy, refers to a palpable reaction or process taking place at a given time and level of intensity. STAI-T, like potential energy, refers to individual differences in reactions. Both of STAI-S and STAI-T scales includes 20 questions. For each question, the scores range from 1 (almost never) to 4 (almost always) points. For both scales, the sum of the scores ranges from 20 to 80. A score between 36 and 41 refers to a mean anxiety level, with values greater than 41 classified as a high level of anxiety. The MDAS consists of 5 questions that measure anxiety at different stages of dental treatment. The options range from 1 (not anxious) to 5 (very anxious) for each question. The sum of the scores varies from 5 to 25; values between 19 and 25 indicate a high level of dental anxiety. The VAS scale was included in the present study to determine how anxious the patients felt according to their own thoughts. Scores range from 0 (no anxiety) to 10 (extreme anxiety). |
Communication after operation
Communication was established after the operation.
|
STAI-S, like kinetic energy, refers to a palpable reaction or process taking place at a given time and level of intensity. STAI-T, like potential energy, refers to individual differences in reactions. Both of STAI-S and STAI-T scales includes 20 questions. For each question, the scores range from 1 (almost never) to 4 (almost always) points. For both scales, the sum of the scores ranges from 20 to 80. A score between 36 and 41 refers to a mean anxiety level, with values greater than 41 classified as a high level of anxiety. The MDAS consists of 5 questions that measure anxiety at different stages of dental treatment. The options range from 1 (not anxious) to 5 (very anxious) for each question. The sum of the scores varies from 5 to 25; values between 19 and 25 indicate a high level of dental anxiety. The VAS scale was included in the present study to determine how anxious the patients felt according to their own thoughts. Scores range from 0 (no anxiety) to 10 (extreme anxiety). |
Communication before and after operation
Communication took place both before and after the operation.
|
STAI-S, like kinetic energy, refers to a palpable reaction or process taking place at a given time and level of intensity. STAI-T, like potential energy, refers to individual differences in reactions. Both of STAI-S and STAI-T scales includes 20 questions. For each question, the scores range from 1 (almost never) to 4 (almost always) points. For both scales, the sum of the scores ranges from 20 to 80. A score between 36 and 41 refers to a mean anxiety level, with values greater than 41 classified as a high level of anxiety. The MDAS consists of 5 questions that measure anxiety at different stages of dental treatment. The options range from 1 (not anxious) to 5 (very anxious) for each question. The sum of the scores varies from 5 to 25; values between 19 and 25 indicate a high level of dental anxiety. The VAS scale was included in the present study to determine how anxious the patients felt according to their own thoughts. Scores range from 0 (no anxiety) to 10 (extreme anxiety). |
No communication
No communication.
|
STAI-S, like kinetic energy, refers to a palpable reaction or process taking place at a given time and level of intensity. STAI-T, like potential energy, refers to individual differences in reactions. Both of STAI-S and STAI-T scales includes 20 questions. For each question, the scores range from 1 (almost never) to 4 (almost always) points. For both scales, the sum of the scores ranges from 20 to 80. A score between 36 and 41 refers to a mean anxiety level, with values greater than 41 classified as a high level of anxiety. The MDAS consists of 5 questions that measure anxiety at different stages of dental treatment. The options range from 1 (not anxious) to 5 (very anxious) for each question. The sum of the scores varies from 5 to 25; values between 19 and 25 indicate a high level of dental anxiety. The VAS scale was included in the present study to determine how anxious the patients felt according to their own thoughts. Scores range from 0 (no anxiety) to 10 (extreme anxiety). |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Visual analog scale (VAS)
Time Frame: 2 weeks
|
The VAS scale was included in the present study to determine how anxious the patients felt according to their own thoughts.
Scores range from 0 (no anxiety) to 10 (extreme anxiety).
|
2 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
State-Trait Anxiety Inventory (STAI-T and STAI-S)
Time Frame: 2 weeks
|
STAI-S, like kinetic energy, refers to a palpable reaction or process taking place at a given time and level of intensity.
STAI-T, like potential energy, refers to individual differences in reactions.
Both of STAI-S and STAI-T scales includes 20 questions.
For each question, the scores range from 1 (almost never) to 4 (almost always) points.
For both scales, the sum of the scores ranges from 20 to 80.
A score between 36 and 41 refers to a mean anxiety level, with values greater than 41 classified as a high level of anxiety.
|
2 weeks
|
Modified Dental Anxiety Scale (MDAS)
Time Frame: 2 weeks
|
The MDAS consists of 5 questions that measure anxiety at different stages of dental treatment.
The options range from 1 (not anxious) to 5 (very anxious) for each question.
The sum of the scores varies from 5 to 25; values between 19 and 25 indicate a high level of dental anxiety.
|
2 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KaradenizTU01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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