03 Ethics in Research Flashcards

1
Q

Generally, research would be deemed ethical if

A

most people would
judge the research to be morally upright.
• It should be more right than some alternative.
• Choose the most ethical option possible instead.
• You should not choose something because it is the least of all evils

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2
Q

research ethics

A

as a standard of conduct for researchers
that distinguishes between acceptable and unacceptable behavior

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3
Q

Types of Concerns

A

Legal vs Illegal
• Ethical vs Unethical
• Moral vs Immoral
• Protecting your participants

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4
Q

Belmont Report (Est. 1979)

A

• Respect for Persons
• Beneficence
• Justice

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5
Q

The Common Rule (Est. 1991) added additional standards for
government-funded research.

A

Compliance
• Informed Consent
• IRB Requirements

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6
Q

• Required elements of data protection:

A

• 1. Notice
• 2. Purpose
• 3. Consent
• 4. Security
• 5. Disclosure
• 6. Access
• 7. Accountability

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7
Q

An error of omission would occur when

A

you fail to disclose information that a
consumer needs in order to understand your research.

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8
Q

The error of commission is

A

any action that is committed in order to mislead.

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9
Q

Types of concerns in ethics

A

legal v. illegal
moral v. immoral
ethical v. unethical

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10
Q

Moral v. immoral

A

We think at the societal level
Minimal ethical guidelines
Morals are based on our beliefs and values

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11
Q

National Research Act of 1974 (the Belmont report)—-1979

A

Were established as a foundation for ethics for research

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12
Q

Core values of the Bellmont Report

A

respect for persons
beneficence
justice

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13
Q

Respect for persons

A

You must hold respect for your participants and treat them as if they are autonomous agents, which means they can make decisions for themselves.

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14
Q

Respect for persons protects certain types of people. Who are those?

A

Helps protect certain classes

People with diminished autonomy/diminished capacity
People who are in prison
Young children—anyone under 18
Mentally retarded
The Insane
Pregnant women

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15
Q

Beneficence

A

You should do no harm to your participants and maximize benefits.
We shouldn’t go in trying to do harm

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16
Q

Justice

A

We should provide fairness and equity in the selection of participants and the treatment of participants.
As fairly as possible

17
Q

Common Rule

A

Gave us guidelines for funding
Rules
Anything funded by the government must be compliant with the policy
Researchers must obtain written informed consent
Need to tell them what is going on
Deception should be minimized
Instiutioms must have an IRB
Approve the study before it goes
Recruitment procedures

18
Q

maintaining privacy

A

Anonymous data
There is no way to link one individual with an answer
Confidential
Link data to person

19
Q

7 Guidelines for maintaining data

A

notice, purpose, consent, security, disclosure, access, accountability,

20
Q

Notice

A

All data subjects should be given notice when data is being collected.
Give as much notice as possible
If there is not an expectation of privacy consent does not need to be given

21
Q

Purpose

A

Only be used for the purpose stated and not for any other purpose.

22
Q

Consent

A

Data should not be disclosed to other parties without consent

23
Q

Security

A

Kept secure from potential abuse
3-5 years after studying

24
Q

Disclosure

A

Should be informed on who is collecting their data

25
Q

Access

A

They need to have access to their data and correct any inaccuracy

26
Q

Accountability

A

Should have some way to hold data collectors accountable
The IRB usually serves as that function.
These are US rules, make sure you are compliant with the laws here and there

27
Q

Compensation

A

You dont want to provide too much compensation
Dont go over 25 because then it could be a brib or encourage those who normally would not participate to participate and harm autonomy