Chapter 2 ppt research - ethics in research

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Last updated 1:42 PM on 9/17/26
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36 Terms

1
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T or F: when it comes to research, there is a history of misconduct

true

2
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___________ __________ is a significant failure to adhere to prevailing, professional standards and is considered a violation of the _________ ___ _________.

research misconduct; code of ethics

3
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_______________ is making stuff up

fabrication

4
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______________ is manipulating research materials, equipment or processes, or altering data or results; not accurately reporting results

falsification

5
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_____________ is using another's ideas

plagiarism

6
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________ __________ is sending your work to multiple sources for publication

self-plagiarism

7
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T or F: it is part of our job to report research misconduct

true

8
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Planning involves ___________, ____________, and __________.

beneficence, respect, and justice

9
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_______________ is making efforts to secure their well being; do no harm; maximize possible benefits and minimize possible harms

beneficence

10
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__________ incorporates at least two ethical convictions; first, that individuals should be treated as autonomous (freedom to choose) agents, and second that persons with diminished autonomy are entitled to protection

respect

11
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____________ ensures the selection of research participants are not based on their easy availability; their compromised position, or their manipulability, rather than for reasons directly related to the problem being studied

justice

12
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________________ is a central tenant of research

confidentiality

13
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why is confidentiality important in research?

to protect participant's from harm, to protect their information, and upholds legal requirements

14
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HIPPA's privacy rule is intended to prevent ___________ or _________ individually identified health info without consent

using or disclosing

15
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What is the smallest penalty given by hippa?

$100 per violation to $25,000 annual

16
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what is the largest penalty given by hippa?

$50,000 per violation to $1.5 million annual

17
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informed consent provides participants with........

enough information to make a reasonable decision if they want to participate in the study or not

18
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informed consent protects the rights of ________________ and the ______________.

participants and the researchers

19
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T or F: if participants include children, additional consideration may be needed, such as child and parental consent

true

20
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T or F: informed consent needs to be straightforward enough for individuals with difficult reading comprehension to understand.

true

21
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If deception is included in a study, what must there be?

a good reason to do so, informed consent must be obtained, additional safeguards to protect participants, and a debriefing at the end of the study

22
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IRB must provide approval of a research proposal ______________ data can be collected/anything can be done.

before

23
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If having a control group, you must plan for when and how they would receive _______________ if they want it

treatment

24
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__________ ___ ___________ is when something could impact or influence a researcher's judgement.

conflict of interest

25
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_____________ is telling people/participants about any financial or personal connection that could affect—or appear to affect—their judgment to reduce conflict of interest

disclosure

26
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When referencing other's intellectual property (direct quotes), you must use _____________.

citation

27
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Why would clinical SLP's need to know how to reference sources?

Clinical SLPs need to know how to reference sources because they use research and other people's ideas in their clinical practice and must give proper credit and avoid plagiarism.

28
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_______________: substantial contribution to conception and design or acquisition of data or analysis and interpretation of data

authorship

29
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________ _________ is the process by which the quality of research is assessed and involves multiple activities

peer reviews

30
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Patients can be _______________ of care in the name of evidence based practice

deprived

31
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T or F: EBP gives more authority to the providers, those who know the research, and less to the patients themselves

true

32
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In ASHA's code of ethics, there are ________ specific references related to research

21

33
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institution review boards are a committee of at least __________ members mandated by the national research act

five

34
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On an IRB board, one must be concerned with _________________ areas

nonscientific

35
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On an IRB board, one member cannot be affiliated with the _________________.

institution

36
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IRB boards are responsible for making decisions _________________ or _____________ research plans

approving or changing