Grace Kelly Ethics Officer Office of Research Ethics The University of Western Ontario

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Grace Kelly Ethics Officer Office of Research Ethics The University of Western Ontario [email protected] x84692 An Introduction to Research Ethics at Western Ethics Considerations for Teachers’ Research with Students in their own Classroom

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An Introduction to Research Ethics at Western Ethics Considerations for Teachers’ Research with Students in their own Classroom. Grace Kelly Ethics Officer Office of Research Ethics The University of Western Ontario [email protected] x84692. Guiding Principles of Research Ethics. - PowerPoint PPT Presentation

Transcript of Grace Kelly Ethics Officer Office of Research Ethics The University of Western Ontario

Page 1: Grace Kelly   Ethics Officer  Office of Research Ethics The University of Western Ontario

Grace Kelly Ethics Officer

Office of Research EthicsThe University of Western Ontario

[email protected] x84692

An Introduction to Research Ethics at Western

Ethics Considerations for Teachers’ Research with

Students in their own Classroom

Page 2: Grace Kelly   Ethics Officer  Office of Research Ethics The University of Western Ontario

Guiding Principles ofResearch Ethics

Page 3: Grace Kelly   Ethics Officer  Office of Research Ethics The University of Western Ontario

Policy Framework

Nuremberg Code, 1949 (end of 2nd world war)

Declaration of Helsinki, 1964 – cornerstone document of human research ethics.

Belmont Report, 1979

PHIPA section 44 -disclosure for research/REB

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TCPS

**Tri-Council Policy Statement (TCPS):

Ethical Conduct for Research Involving Humans, 1998

-Federal Granting Agencies – SSHRC; CIHR; NSERC

-Funding is only given to individuals at institutions that comply with this policy

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TCPSCore PrinciplesWelfare (assess risks and benefits)

Autonomy and Decision Making (informed consent and voluntary participation)

Equal Moral Status of All (inclusive, everyone treated the same)

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How does the TCPS fit into the ORE?

• Based on the Core Principles of the TCPS the ORE’s main goals are as follows:– Protection of human subjects– Assess risks and benefits– Assess research design to ensure minimal

risk and meet objectives– Review subject recruitment to ensure

informed consent– Protect vulnerable groups of individuals

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What Research Goes Where?

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Research Ethics at Western

HSREBFull Board(high risk)

HSREBDelegated Board

(lower risk)Level 1 & Level 2

NMREBNon-MedicalHigher andLower Risk

UWOOffice of Research

Ethics

UWO is the Board of Record for all London Hospitals

UWO Faculty, Staff and Students & institutions

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Assessment of Risk

• Greater scrutiny and expertise required for research that is potentially more invasive or harmful

• REB is responsible for assessing magnitude and probability of potential harms and benefits

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When Do You Need to Apply?

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ALL research involving human subjects and their data must be reviewed by a UWO REB.

This includes all research conducted on campus by UWO Faculty, Staff and Students Research conducted on campus.

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Determining if REB Review is Necessary can be Tricky!

• You wish to conduct a study of the ways in which space and resources are used in the Library– Goal #1: to improve service, see what areas

are used, how could physical space be improved?

– Goal #2: to interview students and staff to understand their perceptions of the library, how important access to materials is to their work, what their demographics are, etc.

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If you’re not sure, please ask.

Everyone’s research is different and unique.

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• If my research requires REB approval• Factor time in as part of research

process– Back and forth process with the ORE

and REB.• Are you the PI of a study? Using UWO

staff, faculty, students or facilities.

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How does the Board Review my Research Proposal?

(From the Guiding Principles)

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What the REB Reviews

• UWO Research Submission (HSREB or NMREB)– Objectives, rationale, hypotheses– Methods, including surveys/instruments– Participants– Confidentiality

• Letter of Information & Consent

• Scripts & Advertisements

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The REB also Reviews…

• Any ‘item’ used to solicit participation in a study including:– Telephone scripts– Recruitment scripts (for on-the-spot surveys)– Cover letters– Email messages– Follow-up/reminder notices (a la Dillman

Method)

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Additionally…The REB Reviews

• All Revisions to already approved research

• FYIs• Adverse Events• Updated Approvals• Protocol Violations• Protocol Deviations

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Sound Methodology• Have you provided support, in the form of

references for your current research question?

• Sample size? Does it work?• Are human participants really necessary to

answer the question?• Clear explanation of steps – also to letter of

information• Do the benefits of the research outweigh the

risks?

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Coercion or Inducements to Participate

• overwhelmed by institutional approval

• fear of loss of health benefits, employment or educational status

• obligation to participate

• financial gain

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Privacy & Confidentiality Issues

• Privacy and confidentiality are recognized as fundamental human rights.

• What counts as loss of privacy may vary from individual to individual and society to society.

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What Constitutes “Identifiers”?

• Name, initials

• Date of birth or death (partial)

• Initials and DOB together

• PINs, OHIP numbers, SIN, others

• Postal code

• Mapping of data

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Assessing Identifiability & Risk

• Identifying information: identifies a specific research participant directly (e.g., name, address, SIN or PIN)

• Identifiable information: could be used to re-identify a participant through a combination of indirect

• De-identified/coded information: Identifiers are removed/replaced with a code. Those with access to the code and the data (or those working directly with those with the code) have identifiable information.

• Anonymized information: Information is irrevocably stripped of identifiers, and a code is not kept

• Anonymous information: Information never had identifiers

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If I need REB Review, do I also always need to obtain

consent?

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Waiver of Consent• Principle of Beneficence• Sheer size• Proportion of individuals relocated or died• Creation of privacy risk by linking ID to de-

identified data• Risk of psychological, social or other harm• Difficulty in contacting individuals• Identifiability

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Waiver of Consent

• Not to be confused with other forms of consent. – Explicit Consent (eg. Completion of Survey)– Explicit Verbal Consent (eg. Telephone

Survey)– Passive Consent (Opt-Out)– Previous Consent

You still need a Letter of Information or script for these forms of consent.

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Informed Consent

• Subjects must be told exactly what is going to happen to them

• Subjects must agree to participate

• Letter of Information

• Consent Form

• Assent Form

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Informed Consent Guidance

HSREB & NMREB GUIDELINEShttp://www.uwo.ca/research/ethics/

•Required Wording•Letter explains clearly the study methods•What will be done with the data •Participant confidentiality/anonymity•Participant contact information•Grammar & Spelling

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Teachers’ Research with Students in their own Classroom

The main issue that exists when a teacher wants to conduct research in their own classroom is the power relationship that exists between a teacher and her/his own students and even further – the issue of coercion.

However…..

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Teachers’ Research with Students in their own Classroom

• …with proper planning and consideration a teacher may be able to use the students within his/her own class as study participants provided (s)he is able to avoid both the reality and appearance of coercion and coercion itself.

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Step 1

• When thinking about your research, distinguish between activities that constitute ‘research’ and those that fall under ‘professional development’. – Look back at our examples of whether or not

ethics is needed. • If not publishing and only examining the teacher’s

pedagogical practices then no ethics is needed.• If publishing best to get ethics approval

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Step 2

• Decide how you will avoid both the reality and perception of coercion– A potential ‘risk’ in these studies is being

coerced into participating in a study in which one does not want to participate.

• (eg. Parents or students feel obligated to participate to avoid offending teacher or so that the child’s marks are not affected).

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Step 3• Create a plausible plan for avoiding

coercion in your submissions. – Alternatives forms of data collection should be

made to avoid coercion. • Anonymous online questionnaire

• Study students in a different classroom

• Use another researcher to do the research for you (3rd party) – they collect consent and keep results until final grades submitted, therefore teacher doesn’t know who participated and can’t base grades on that

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Summary• Careful consideration must be taken to

avoid any undue influence on the participant which will undermine the voluntary character of the consent.

• Where possible, the approach to the participant inviting to participation in a research project should be made by someone not in a position of authority over the subject.

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Summary

• Students must be assured that withdrawal will not result in any academic penalty.

• Similarly students should not be promised academic reward.