- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03051295
Dentists' Understanding of Diagnostic Test Results and Treatment Efficacy. (RCDENT2017)
February 10, 2017 updated by: Paulo Nadanovsky, Rio de Janeiro State University
The Influence of Different Formats for Presenting Diagnostic Test Results and Treatment Efficacy on Dentists' Understanding and on Their Reported Clinical Management.
There is little evidence on how best to present diagnostic and treatment effect information to dentists and whether this makes any difference to their understanding of the information given and clinical management.
The objective of this study is to assess the influence of different formats for presenting diagnostic test results and treatment efficacy on dentists' understanding and on their reported clinical management.
The hypothesis is that presenting diagnostic test and treatment effectiveness results using natural frequencies influences the threshold for treatment and improves interpretation of tests results compared to conditional probabilities and percentage differences.
A group of dentists recruited from postgraduate courses were randomized to two of four arms, being two arms of a hypothetical realistic diagnostic scenario (a) and two arms of a hypothetical realistic treatment scenario (b): a1) diagnostic test results presented in conditional probabilities; a2) diagnostic test results presented in natural frequencies; b1) treatment efficacy presented in percentages; b2) treatment efficacy presented in natural frequencies.
The main outcome measures were the correct answer as to whether disease was actually present (post-test probability) and the correct answer as the number of patients that would benefit from the treatment (efficacy).
Secondary outcome measures included the decision whether to treat or not treat the hypothetical patient.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
101
Phase
- Not Applicable
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Graduated dentist undergoing a postgraduate course in a public university in Rio de Janeiro.
Exclusion Criteria:
- None.
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
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Diagnostic percentages.
Dentist receives diagnostic test results presented in conditional probabilities.
|
The format in which dentists receive information about diagnostic test results and efficacy of treatment.
|
|
Experimental: Diagnostic frequencies
Dentist receives diagnostic test results presented in natural frequencies.
|
The format in which dentists receive information about diagnostic test results and efficacy of treatment.
|
|
Active Comparator: Treatment percentages.
Dentist receives treatment efficacy presented in percentages.
|
The format in which dentists receive information about diagnostic test results and efficacy of treatment.
|
|
Experimental: Treatment frequencies.
Dentist receives treatment efficacy presented in natural frequencies.
|
The format in which dentists receive information about diagnostic test results and efficacy of treatment.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The probability that a patient will have a dental cavity as assessed by a dentist.
Time Frame: Up to 20 minutes
|
The assessement by the dentist was based on a questionnarie containing a clinical hypothetical situation and the result of a bite-wing radiographic exam.
|
Up to 20 minutes
|
|
The number of patients that will benefit from systemic antibiotics adjunct to periodontal treatment as assessed by a dentist.
Time Frame: Up to 20 minutes
|
The assessement by the dentist was based on a questionnarie containing a clinical hypothetical situation and the information about the usual efficacy of systemic antibiotics adjunct to periodontal treatment.
|
Up to 20 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The number of dentists that would recommend the use of systemic antibiotics adjunct to periodontal treatment in the clinical management of a patient with periodontal disease.
Time Frame: Up to 20 minutes
|
The recommendation by the dentist was based on a questionnarie containing a clinical hypothetical situation and the information about the usual efficacy of systemic antibiotics adjunct to periodontal treatment.
|
Up to 20 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
June 8, 2016
Primary Completion (Actual)
December 13, 2016
Study Completion (Actual)
December 13, 2016
Study Registration Dates
First Submitted
February 6, 2017
First Submitted That Met QC Criteria
February 10, 2017
First Posted (Actual)
February 13, 2017
Study Record Updates
Last Update Posted (Actual)
February 13, 2017
Last Update Submitted That Met QC Criteria
February 10, 2017
Last Verified
February 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- riskcommunicationdentist2017
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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