- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00981019
Doctors' Understanding of Survival Statistics (MPIB)
July 20, 2011 updated by: Max Planck Institute for Human Development
Study of Primary Care Physicians' Understanding and Use of Different Survival Measures
The probably most commonly used measure for expressing the pay-offs of early detection and treatment are survival rates.
Yet, over time and groups this metric comes with several biases and thus, is not reliable for judging such benefits.
Epidemiologists recommend using reduction of disease-specific mortality rates instead, which is unbiased.
The purpose of the study is to investigate how primary care physicians understand and use different survival measures for determining the benefit of cancer screening tests.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
778
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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Berlin, Germany, 14195
- Max Planck Institute for Human Development
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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 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
301 primary care physicians (internal, general, and family medicine physicians)
Description
Inclusion Criteria:
- primary care physicians (internal, general, and family medicine physicians)
Exclusion Criteria:
- all other types of physicians
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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mortality*incidence*5-year survival*early stage
Physicians will be faced in scenarios about screening with information on mortality and 5-year survival, followed by information on mortality*incidence and 5-year survival*early stage in a random order.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of Physicians (=Participants) Recommending the Screening
Time Frame: 25 minutes (mean duration of the survey)
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The aim of the study was to learn how different medical cancer screening statistics would influence doctors' recommendation behavior and their effectiveness judgments of screening tests.
For that reason the online survey study presented physicians with four different medical statistics (e.g., 5-year survival) within four successive scenarios and asked after each scenario whether they would recommend the screening to a (hypothetical) patient given the data.
Options to answer are: Definitely yes, Probably yes, Probably no, Definitely no, Can't decide.
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25 minutes (mean duration of the survey)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of Physicians (= Participants) Assuming a Benefit of Screening
Time Frame: 25 minutes (mean duration of the survey)
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Physicians are faced with four different medical statistics about the effect of screening (e.g., 5-year survival) within four successive scenarios and after each scenario asked whether they assume the screening to be beneficial given the statistical information.
Options to answer are: yes, no, can't decide.
If yes, then participants are further asked to describe this benefit by the following categories: Very large, large, moderate, small, very small.
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25 minutes (mean duration of the survey)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Odette Wegwarth, Dr., Max Planck Institute for Human Development
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
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
December 1, 2009
Primary Completion (Actual)
December 1, 2009
Study Completion (Actual)
December 1, 2009
Study Registration Dates
First Submitted
September 18, 2009
First Submitted That Met QC Criteria
September 21, 2009
First Posted (Estimate)
September 22, 2009
Study Record Updates
Last Update Posted (Estimate)
August 15, 2011
Last Update Submitted That Met QC Criteria
July 20, 2011
Last Verified
July 1, 2011
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- MPIB-01-SM
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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