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Thank you for assisting in our research.
Currently we preparing for our next phase of testing. Please click "I consent" below to view a DEMO of our survey.
By clicking "I consent" you indicate the following:
I am at least 18 years old; I understand and agree to the following conditions; my questions have been answered satisfactorily; and I have printed a copy of this study information sheet for my records.
I consent I do not consent
The IUPUI/Clarian Research Compliance Administration has approved the following study:
"The Impact of Human Likeness on Ethical Decision-Making in Online
Interactions" (No. EX0805-32B)
Approval date: May 28, 2008
Expiry date: May 27, 2009
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Purpose: The
purpose of this study is to determine the effects of confronting ethical dilemmas in an electronic context.
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Benefits: The data gathered may contribute to an understanding of how medical ethics are or can be communicated electronically.
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Procedure:
You will take the role of doctor in an office consultation with a patient. You will reply to the patient by selecting an appropriate response from a list. The situation will present an ethical dilemma. After the consultation, you will make a decision on the dilemma. Finally, there is a word completion task and survey on your religious beliefs.
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Time required: About 15 minutes
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Participation: Participation is voluntary. You may refuse to participate at any time. No disadvantage will
arise from refusing. Incomplete results are retained.
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Age restriction: You must be at
least 18 years old to participate.
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Compensation: You will not be paid
for participating.
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Confidentiality: Your personal
information will not be identified or shared or used for another purpose.
Reported results will not contain information that may be used to identify
you.
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Risks: While we do not anticipate
any risks from participating, you must stop participating and notify the
principal investigator if at any time you feel your mental or physical
well-being, personal values, or dignity is being harmed.
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Dissemination of results: Results
may be reported in talks, documents, and publications of the principal
investigator, experimenter, and their co-authors.
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Questions:
If you have any questions or concerns about the study, feel free to
contact the principal investigator, Prof. Karl F. MacDorman. If you
have any questions about your rights as a research participant, or
unresolved problems, complaints, or concerns about a study, contact the
IUPUI/Clarian Research Compliance Administration. Contact details are
provided on the contact webpage.
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