- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01665313
Comparison of Attention of Physician After Outpatient Clinic
July 25, 2013 updated by: Seoul National University Hospital
Comparison of Performance, Attention, and Emotion of Physician Before and After Outpatient Clinic Session
The attention and clinical performance of physician might be decreased after outpatient clinic session compared to those measured before outpatient clinic.
Study Overview
Status
Completed
Conditions
Detailed Description
A large body of data shows that fatigue impairs human performance.
Additionally, many studies have provided evidence that fatigue can worsen mood, as indicated by increased scores on measures of depression, anxiety, confusion, and anger.
In this context, we examined attentional and emotional changes in physicians after they completed an overwhelming outpatient clinic in a university-affiliated tertiary referral hospital in South Korea.
Study Type
Observational
Enrollment (Actual)
46
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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Seoul, Korea, Republic of
- Seoul National University Hospital
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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
30 years to 59 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
physicians with outpatient clinic sessions in Seoul National University Hospital
Description
Inclusion Criteria:
- physicians with outpatient clinic sessions in Seoul National University Hospital
- age 30~59
- internal part or external part
Exclusion Criteria:
- physicians who do not agree to participate in the study
- physicians who are taking drugs known to affect the sleep/wake cycle or daytime alertness
- physicians who have current psychiatric illness or sleep disorder
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 |
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participants
Full-time faculty with morning and afternoon outpatient clinics on the same day in SNUH
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
difference of response time in PVT(Psychomotor vigilance task) before and after outpatient clinic session
Time Frame: change from baseline in response time in PVT after opd session (average 7hours)
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change from baseline in response time in PVT after opd session (average 7hours)
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
frequency of physician's clinical mistakes during morning and afternoon session in outpatient clinic
Time Frame: for the duration of opd session, average up to 7hours
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for the duration of opd session, average up to 7hours
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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
July 1, 2012
Primary Completion (Actual)
January 1, 2013
Study Completion (Actual)
January 1, 2013
Study Registration Dates
First Submitted
July 8, 2012
First Submitted That Met QC Criteria
August 13, 2012
First Posted (Estimate)
August 15, 2012
Study Record Updates
Last Update Posted (Estimate)
July 26, 2013
Last Update Submitted That Met QC Criteria
July 25, 2013
Last Verified
July 1, 2013
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- attention_SNUH
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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