Research Flashcards

1
Q

16.1 recognized standards

A

A registrant must design, conduct, and report on research in accordance with recognized standards of scientific competence and ethical research.

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2
Q

16.2 Avoiding misleading results

A

A registrant must plan their research to minimize the possibility of misleading results.

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3
Q

16.3 ethical considerations

A

In planning research, a registrant must take into account any applicable ethical considerations.

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4
Q

16.4 resolution of ethical issues

A

If application of an ethical issue is unclear, a registrant must seek to resolve the issue through consultation with institutional review boards, animal care and use committees, peer consultation, or consultation with other appropriate resources.

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5
Q

16.5 ethical conduct of research

A

A registrant is responsible for the ethical conduct of research conducted by themself or by others under their supervision or control.

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6
Q

16.6 protection of animals/human welfare

A

In research projects, a registrant must implement appropriate protections for the rights and welfare of human participants and other persons affected by the research, and for the welfare of animal subjects.

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7
Q

16.7 Offering research inducements

A

If a registrant offers professional services as an inducement to obtain research participants, a registrant must make clear to the participants the nature of the professional services offered, including any risks associated with and limitations to such services.

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8
Q

16.8 Unacceptable inducements

A

A registrant must not offer excessive or inappropriate financial or other inducements to obtain research participants, particularly if such inducements may be expected to coerce participation.

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9
Q

16.9 Competent research

A

A registrant must conduct research competently and with due concern for the dignity and welfare of the participants.

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10
Q

16.10 Required consultations

A

As part of the process of development and implementation of research projects, a registrant must consult those with expertise concerning any special population that is under investigation or that is likely to be affected by the research.

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11
Q

16.11 Compliance with law

A

A registrant must plan and conduct research in a manner consistent with international, federal and provincial laws and with professional standards governing the conduct of research, particularly those standards governing research with human participants and animal subjects.

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12
Q

16.12 Institutional approval

A

Before conducting research, a registrant must:
a) provide accurate information about their research protocol in a
research proposal to the host institution or organization; and
b) obtain appropriate approval from the host institution or organization.

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13
Q

16.13 Research in accordance with protocol

A

A registrant must conduct their research in accordance with any research protocol approved under Standard 16.12.

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14
Q

16.14 information to participants

A

A registrant must provide a prompt opportunity for research participants to obtain appropriate information about the nature, results, and conclusions of the research, including any information necessary to correct any misconceptions the participants may have.

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15
Q

16.15 Exception to information to participants

A

If scientific or humane values justify delaying or withholding the information referred to in Standard 16.14, a registrant must take measures to reduce the risk of harm.

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16
Q

16.16 Appropriate interference

A

In conducting research, a registrant must only interfere with the research participants or the milieu from which data is collected in a manner that is warranted by an appropriate research design, and consistent with the registrant’s role as a scientific investigator

17
Q

16.17 Honouring commitments

A

A registrant must honour all commitments they have made to research participants.

18
Q

16.18 No false reporting

A

A registrant must not fabricate or falsify research data or results, or exaggerate the meaning and/or significance of any research data or results.

19
Q

16.19 Errors in reporting

A

If a registrant discovers significant errors in their published data, the registrant must take steps to correct such errors in a correction, retraction, erratum, or by other appropriate publication means.

20
Q

16.20 Professional reviews

A

A registrant who reviews material submitted for publication, grants, or research proposal review must respect the confidentiality of the information and the proprietary rights of the submitter in that information.

21
Q

15.10 Supervision in multidisciplinary settings

A

A registrant in a supervisory role over a non-registrant in a multidisciplinary/collaborative care setting is responsible for ensuring they:
a) provide supervision only for that work for which each non-registrant has the appropriate background, training, and experience;
b) clarify their obligations as a supervisor with their employer, if any, and with their supervisee(s) regarding documentation of supervision, providing feedback to supervisees, reporting of supervisee activities, and any other elements of the supervision;
c)
maintain compliance with all other requirements in this Code pertaining to supervisory services.