- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04030975
Cognitive Process of Diagnostic Error in Emergency Physicians (diagnosis)
July 22, 2019 updated by: Cathay General Hosp. IRB, Cathay General Hospital
Diagnostic error, Dual process model of reasoning) During the last decade, much emphasis has been placed on system solutions to patient safety problems.
However, diagnostic error, despite being responsible for twice as many adverse events as medication error, has received little attention.
The rate of diagnostic errors have been estimated to be between 0.6% to 12%.Some estimates are as high as 15%.The rate of negative outcome or adverse effects of diagnostic errors range from 6.9% to 17%.
Most authors accept that the dual process model of reasoning explains how clinicians make diagnoses.
The purpose of this study is to investigate why diagnostic errors occurred in the emergency departments (EDs).
Study Overview
Status
Completed
Conditions
Detailed Description
Diagnostic error, Dual process model of reasoning) During the last decade, much emphasis has been placed on system solutions to patient safety problems.
However, diagnostic error, despite being responsible for twice as many adverse events as medication error, has received little attention.
The rate of diagnostic errors have been estimated to be between 0.6% to 12%.Some estimates are as high as 15%.The rate of negative outcome or adverse effects of diagnostic errors range from 6.9% to 17%.
Most authors accept that the dual process model of reasoning explains how clinicians make diagnoses.
The purpose of this study is to investigate why diagnostic errors occurred in the emergency departments (EDs).
A qualitative study approach was used with in-depth semi-structured interviews conducted with emergency physicians to investigate the cognitive diagnosis process.
The study takes place in the EDs of three hospitals in Taiwan.
We chose the participants using a purposive sampling technique to yield a sample that would be most likely contribute significant information on the diagnostic process.
Sampling continued until novel information was no longer being gathered.
All audiotapes were transcribed verbatim.
The transcripts are analyzed by two of the investigators based on the ground theory.
Once all relevant codes were identified, they were grouped together into meaningful categories.
These categories were then grouped under appropriate themes, which were used to generate a theory of diagnostic errors.
Study Type
Observational
Enrollment (Actual)
30
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
-
-
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Taipei, Taiwan, 10630
- Cathay hospital
-
-
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
21 years to 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
emergency physicians
Description
Inclusion Criteria:
- trained emergency physicians
Exclusion Criteria:
- refused interview
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 |
|---|
|
interview
emergency physicians
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
generate a theory of diagnostic errors
Time Frame: Dec., 2015
|
Dec., 2015
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Chaou-Shune Lin, MD, Hsinchu Cathay General Hospital
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
May 1, 2014
Primary Completion (ACTUAL)
November 1, 2015
Study Completion (ACTUAL)
November 1, 2015
Study Registration Dates
First Submitted
May 27, 2014
First Submitted That Met QC Criteria
July 22, 2019
First Posted (ACTUAL)
July 24, 2019
Study Record Updates
Last Update Posted (ACTUAL)
July 24, 2019
Last Update Submitted That Met QC Criteria
July 22, 2019
Last Verified
July 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CGH-P103018 (OTHER: CGH)
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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