Ethical Issues (RM2) Flashcards

(44 cards)

1
Q

What is the primary duty of psychologists in research?

A

Duty of care

Psychologists study people and must ensure ethical standards in all aspects of research.

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2
Q

According to the British Psychological Society (BPS), what must investigators consider in their research?

A

Ethical implications and psychological consequences

This consideration is crucial for the well-being of research participants.

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3
Q

List the nine aspects of ethics covered by the BPS code of ethics.

A
  • Consent
  • Deception
  • Debriefing
  • Withdrawal from investigation
  • Confidentiality
  • Protection of participants
  • Observational research
  • Giving advice
  • Colleagues

These aspects guide ethical conduct in research with human participants.

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4
Q

True or false: Participants should be misled during psychological research.

A

FALSE

Deception is not allowed; participants should not be misled.

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5
Q

What should happen after a psychological investigation according to the BPS code?

A

Debriefing

The study should be discussed with participants following the investigation.

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6
Q

What right do participants have regarding their involvement in research?

A

Right to withdraw

Participants should feel free to leave the investigation at any time.

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7
Q

What is the role of an ethics committee in psychological research?

A

Provide guidance on ethical responsibilities

They ensure research aligns with the BPS Code of Human Research Ethics.

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8
Q

What must researchers obtain from the ethics committee before conducting research?

A

Approval for their research

This ensures that the research adheres to ethical guidelines.

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9
Q

What do ethics committees assess when research may not fully abide by ethical guidelines?

A

Cost-benefit analysis

They weigh the value of the research against potential costs to participants.

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10
Q

Fill in the blank: Most ethical issues can be avoided by gaining _______ from potential participants.

A

informed consent

This ensures participants understand the research before agreeing to take part.

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11
Q

What does the BPS code state about confidentiality?

A

Participants have the right to confidentiality

This protects participants’ private information during research.

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12
Q

What is the responsibility of psychologists regarding giving advice?

A

Only give advice for which they are qualified

This ensures that advice is based on expertise and ethical standards.

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13
Q

What is the ethical consideration regarding observational research?

A

Respect the privacy of participants

This is crucial to maintain ethical standards in research.

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14
Q

What is the primary ethical issue in psychological research?

A

Conflict between conducting research and respecting participants’ dignity and wellbeing

Researchers aim to produce valid data while ensuring participant rights are upheld.

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15
Q

What is informed consent in the context of psychological studies?

A

Participants are informed about the study’s aims, procedures, rights, and data usage

Participants must make an informed judgment without feeling coerced.

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16
Q

What must be included in a consent form for participants?

A
  • Aims and procedures of the study
  • Participants’ rights (including right to withdraw)
  • Data usage information

Consent forms ensure participants understand what they are agreeing to.

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17
Q

What is presumptive consent?

A

Asking similar individuals if they would consider the research acceptable

If they agree, it is assumed that actual participants would also agree.

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18
Q

What is prior general consent?

A

Asking volunteers general questions about potential participation in misleading studies

This helps gauge willingness before actual participation.

19
Q

What is retrospective consent?

A

Debriefing participants after the study and asking for consent to use their data

Participants can withdraw their data if they do not consent post-study.

20
Q

What is the ethical issue of deception in research?

A

Deliberately misleading or withholding information from participants

Participants cannot give informed consent if deceived.

21
Q

How should researchers handle deception in studies?

A
  • Provide as much information as possible in instructions
  • Debrief participants with true study aims
  • Reassure participants about their behavior

Counseling should be offered if participants feel distressed due to deception.

22
Q

True or false: Researchers can always use deception in studies without any justification.

A

FALSE

Deception must not cause undue distress and requires ethics committee approval.

23
Q

What is the relationship between informed consent and deception?

A

Deception prevents informed consent as participants cannot make informed decisions

Ethical guidelines emphasize transparency to uphold participant rights.

24
Q

What is the researcher’s responsibility regarding participants’ protection from harm?

A

To protect participants from physical and psychological harm, including embarrassment and stress

The risk of harm must be no greater than in ordinary life.

25
How should a researcher ensure **participants' safety** during a study?
By making procedures safe and ensuring participants are aware of their right to withdraw ## Footnote Participants can stop their participation if they feel they are experiencing harm.
26
If a researcher suspects that a study is causing **harm**, what should they do?
Terminate the research even if the participant has not asked to withdraw ## Footnote This includes undue stress, anxiety, or anger.
27
What is the purpose of a **debrief** after a study?
* Complete participants' understanding of the study * Monitor unforeseen negative effects * Find out if anything upset the participant ## Footnote Participants should leave the study in the same state as they entered.
28
What should researchers provide if participants require it after a study?
Counseling or a referral to a qualified counselor ## Footnote This is necessary if participants have experienced harm.
29
Under the **data protection act**, what rights do participants have regarding their personal data?
* Right to have personal data protected * Right to confidentiality * Right to control information about them ## Footnote Information should not be traceable back to participants.
30
How should researchers maintain **anonymity** in reports?
By not naming participants and referring to them as Participant 1, Participant 2, etc. ## Footnote This is most common in case studies.
31
What should participants be reminded of in the **consent form**?
Their right to withdraw from the study ## Footnote This reminder should also be included in standardized instructions and debrief.
32
True or false: Participants can withdraw their results from the study after completion.
TRUE ## Footnote Participants should be informed they can stop their participation at any point.
33
What should be included in the **debrief** for participants?
* Aims and procedures of the study * Reminder of rights, including right to withdraw * Explanation of data usage ## Footnote Parents should also be debriefed if participants are under 16.
34
What should a **consent form** include regarding procedural points?
* Description of the task participants are expected to do * Check participants' understanding of what they are being asked to do * Ask if they have any questions? ## Footnote These points ensure participants are fully informed about their involvement in the study.
35
What are the **ethical points** that must be included in a consent form?
* No pressure to consent * Ability to withdraw at any time * Ability to withdraw data from the study * Data will be kept confidential and anonymous * Full debrief at the end of the study * Space for participants to sign and date ## Footnote Ethical considerations are crucial to protect participants' rights and well-being.
36
True or false: Participants can withdraw their data from the study at any time.
TRUE ## Footnote Participants have the right to withdraw their data even after the study is complete.
37
What is the **main aim** of the study mentioned in the consent form?
To test the psychological consequences of medical conditions and interventions ## Footnote The study compares data from healthy participants with groups of patients suffering from heart and liver disease.
38
What types of tests will participants complete during the study?
* Three brief tests of attention * Memory test * Concentration test * Two questionnaires assessing emotional state and quality of life * Brief driving simulation test ## Footnote The entire procedure is designed to last approximately one hour.
39
Fill in the blank: Consent forms must be written in a suitably **_______** tone.
formal ## Footnote A formal tone ensures clarity and professionalism in the consent process.
40
What should participants understand about their **participation** in the study?
* Participation is voluntary * They may withdraw at any time without penalty * They understand what their participation involves * All questions about the study have been satisfactorily answered ## Footnote This understanding is crucial for informed consent.
41
True or false: Participants can still **withdraw** from the investigation after the study.
TRUE ## Footnote Participants have the right to withdraw their data at any time.
42
What should participants do if they feel they have suffered any **psychological harm**?
Contact the researcher for further help and support ## Footnote The researcher will refer them to appropriate resources.
43
What should participants do if they have any **questions** about the study?
Feel free to ask the researcher ## Footnote Participants are encouraged to seek clarification on any aspect of the study.
44
Do participants still consent to their results being used for the **study**?
Yes, they need to confirm their consent ## Footnote Consent is an ongoing process throughout the study.