Ethics in Research: Chapter 4 Flashcards
1
Q
responsibility toward participants
A
- ensure the welfare, dignity, safety
- for human and nonhuman research participants and
subjects.
2
Q
responsibility toward science
A
ensure that public reports of research are accurate and honest.
3
Q
historical roots of ethics
A
- Milgram experiment
- Nuremburg Code
- Amercian Psychological Association
- National research act
- Belmont report
4
Q
Belmont Report: three core principles
A
-respect of persons
- beneficence
- justice
5
Q
Tricouncil of Policy Statements
A
- Canadian Institutes of Health Research (CIHR)
- Natural Sciences and Engineering Research
Council of Canada (NSERC) - Social Sciences and Humanities Research
Council of Canada (SSHRC)
6
Q
Tricouncil Policy Statement: core principles
A
- respect for persons
-concerns for welfare (beneficence) - justice
7
Q
ethical principles
A
- no harm
- informed consent and deception
- anonymity and confidentiality
8
Q
no harm
A
- Participants must be informed of what will be
done to them & why (purpose of the study). - Right to withdraw at any time, without consequence.
- Participation must be voluntary and not coerced.
9
Q
informed consent
A
- assent is necessary from children and vulnerable populations
- consent is necessary from guardians
- for indigenous populations, consent is required from the community’s gatekeepers
10
Q
deception
A
- Passive: leave out information.
- Must always debrief participants immediately afterward.
- Active: alter information (e.g., false feedback) or confederates
- placebo: inform participants that they may or
may not be in this group
11
Q
anonymity
A
- Data shared should not allow for the
identification of an individual - Assign code numbers or
pseudonyms - Only group data is reported
12
Q
confidentiality
A
- Access to the data is limited to the research
team. - Password-protected files, encryption, and hard copies in locked file cabinets
13
Q
public information and consent
A
- the information is legally accessible to the
public and appropriately protected by law - the information is publicly accessible and
there is no reasonable expectation of
privacy.
14
Q
consent is not required when…
A
- there is no intervention staged by the
researcher, or direct interaction with the
individuals or groups - there is no reasonable expectation of
privacy - dissemination of research results
does not allow the identification of specific
individuals.
15
Q
the internet and consent: major issues
A
- Expectation of privacy
- Persistence & traceability of quotes