- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03596255
Clinical Estimation of Dental Anxiety
July 20, 2018 updated by: Markus Höglund, Karolinska Institutet
Introduction: Dental anxiety (DA) is treatable and preventable when dental personnel correctly estimate the patient's level of DA.
Objective: To evaluate dental personnel's ability to estimate DA.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Method: All public dental clinics in the region of Östergötland, Sweden, were asked to consecutively recruit adult patients returning for their annual examination.
The patient rated DA using the Modified Dental Anxiety Scale (MDAS) and a Visual Analogue Scale of dental anxiety (DA-VAS).
The patient also recorded gender, age, level of education and confidence in handling DA.
After the examination, the dental personnel estimated the patient's level of DA (eDA) on a VAS.
The examiner also recorded gender, age, profession, years of experience, country of education, interest in DA, special education concerning DA and confidence in ability to handle DA.
Study Type
Observational
Enrollment (Actual)
1230
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
-
-
Östergötland
-
Linköping, Östergötland, Sweden, 58212
- Centrum för Orofacial Medicin, Torkelbergsgatan 11.
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
All adult patients returning for their annual examination on a public dental clinics in the region of Östergötland, Sweden
Description
Inclusion Criteria:
Adult patients returning for their annual examination on a public dental clinics in the region of Östergötland, Sweden during a two week period.
Exclusion Criteria:
inability to fill in the questionnaire
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
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Patients
All public dental clinics in the region of Östergötland, Sweden, were asked to consecutively recruit adult patients returning for their annual examination
|
The patient rated their DA using the Modified Dental Anxiety Scale (MDAS)
|
Dental personnel
All public dental clinics in the region of Östergötland, Sweden were contacted and asked to participate in the study
|
the dental personnel estimated the patient's level of DA (eDA) on a 100mm VAS
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Estimated Dental anxiety on a 100mm VAS vs MDAS
Time Frame: through study completion, 2 weeks/clinic and a total of aproximatly 6 months
|
The dental personnel's Clinical estimation of how dentally anxious their patient are (where 0mm represent minimal and 100mm maximal.)
compared to the patients one rating of dental anxiety(Measured whit the Modified Dental Anxiety Scale(MDAS) where 5 is minimal and 25 maximal) .
|
through study completion, 2 weeks/clinic and a total of aproximatly 6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The patients Dental Anxiety, measured whit the "Modified Dental Anxiety Scale"(MDAS)
Time Frame: through study completion, 2 weeks/clinic and a total of approximately 6 months
|
The Patients own ration of how dentally anxious they are.
Measured whit the Modified Dental Anxiety Scale(MDAS) where 5 is minimal and 25 maximal
|
through study completion, 2 weeks/clinic and a total of approximately 6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Director: Mats Bågesund, Lecturer, Linköpings University, Sweden.
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)
September 1, 2017
Primary Completion (Actual)
December 20, 2017
Study Completion (Actual)
February 1, 2018
Study Registration Dates
First Submitted
June 27, 2018
First Submitted That Met QC Criteria
July 20, 2018
First Posted (Actual)
July 23, 2018
Study Record Updates
Last Update Posted (Actual)
July 23, 2018
Last Update Submitted That Met QC Criteria
July 20, 2018
Last Verified
July 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0001 (Cancer Research Institute)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
IPD Plan Description
Data will only be presented at group level.
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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