c1: Key science skills and research methods in psychology Flashcards
define primary data
information collected directly from the source by the researcher (or through others) for their own specific purpose FOR THE FIRST TIME
define secondary data
information that was not collected directly by the current researcher but was collected
at an earlier time by someone else. It has already been collected by some other individual, group or organisation and will not be used for the first time, which is why it is referred to as ‘secondary’
define objective data
information that is observable, measurable, verifiable and free from the personal bias of the researcher
objective data preferred in science
define subjective data
information that is based on personal opinion, interpretation, point of view or judgment
determined by the research participants and cannot always be verified by the researcher
It is often biased, can vary from person to person, day to day from the same person, and is not always entirely accurate.
what are ethical concepts
beneficence, integrity, justice, non-maleficence, respect
what are the ethical guidelines
confidentiality, debriefing, informed consent, use of deception, voluntary participation, withdrawal rights
define beneficence
commitment to maximising benefits and minimising the risks and harms involved in taking a particular position or course of action
- the researcher must consider and maximise all possible good outcomes while minimising the risks of harm to participants and to the community in general
- potential benefits must justify any risk or harm or discomfort to participants
define integrity
the commitment to searching for knowledge and understanding, the honest reporting of all sources of information and results, whether favourable or unfavourable, in ways that permit scrutiny and contribute to public knowledge and understanding.
research that is conducted w integrity must be carried out w a commitment to the following recognised ethical principles and guidelines:
accurate and responsible reporting of findings, whether the results are favourable or unfavourable.
define justice
- The moral obligation to ensure that there is fair consideration of competing claims
- no unfair burden on a particular group from an action; and that there is fair distribution and access to the benefits of an action
what must a researcher do to ensure justice when conducting an experiment
- researcher must use fair procedures and ensure fair distribution of costs and benefits
- process of recruiting and selecting participants should be fair so the researcher must avoid imposing on particular groups an unfair burden of participation in their research
- benefits of the research should be distributed fairly between the participants and the wider community
define non-maleficience
- Involves avoiding the causations of harm
- However, as positions or courses of actions in scientific research may involve some degree of harm, the concept of non-maleficence implies that the harm resulting from any position or course of action should not be disproportionate to the benefits from any position or course of action
- the researcher must strive to ensure that there are benefits from their research and take care to not only avoid harm to all participants but to protect them from harm
- If there is any potential for harm, then it must be justifiable and outweighed by the benefits.
define respect
- Involves consideration of the extent to which living things have an intrinsic value and/or instrumental value; giving due regard to the welfare, liberty and autonomy, beliefs, perceptions, customs and cultural heritage of both the individual and the collective
- consideration of the capacity of living things to make their own decisions; and when living things have diminished capacity to make their own decisions ensuring that they are empowered where possible and protected as necessary.
- example:
- the researcher must recognise that all individuals, both human and non-human, have value and importance.
- In relation to people, the researcher must take account of the rights, beliefs, perceptions and cultural backgrounds of all participants and the groups to which they belong
- all participants have the rights to
- privacy
- confidentiality
- make informed decisions about matters that affect them
- People must be protected and empowered if they are vulnerable or their capacity to make informed decisions is impaired (example: children)
- all participants have the rights to
define confidentiality
- The privacy, protection and security of a participant’s personal information in terms of personal details and the anonymity in individual results, including the removal of identifying elements.
what must a researcher do to ensure confidentiality
the obligation of the researcher not to use or disclose private information for any other purpose
- Participants have a right to privacy, so the researcher must collect only the information that is needed
- any information that may identify an individual or their involvement in research (e.g. personal data) cannot be revealed unless consented
- The right to privacy and procedures for establishing and maintaining confidentiality must be explained to participants before the study commences
- also applies to the collection, recording, accessing, storage, dissemination and disposal of personal information
- If personal information about an individual is no longer needed, then the information should be destroyed or de-identified.