Midterm Flashcards
(104 cards)
Constructivism
Knowledge generated by individual perception, construction of reality
Methodology
Systematic process used to gather information
Epistemology
Beliefs about how knowledge is generated
Fidelity
Consistency with which a treatment is delivered
Peer reviewed articles
Published in established journals, accepted under double-blind peer review process (meaning authors and reviewers are unknown to each other)
Types of literature review
Linear versus integrated
Goals of literature review
What is known and what still needs to be learned
Linear literature review
Organized by study (a named and then summarized)
Integrated literature review
Research organized by topic, each topic summarized noting confirming and disconfirming evidence from individual studies
Experimental research design
Makes comparisons between groups. True experimental means groups are randomly assigned and there is a control group
Pre-experimental research design
No random assignment and no control group, not generalizable. Single group: pre-test, intervention, post-test
Quasi-experimental research design
Control group but no random assignment. Used to describe differences between preexisting groups, where assignment can’t be random. (independent variable cannot be manipulated)
Correlational research design
Most dominant form. Explores how phenomena relate to each other, no need for control group. Usually involves regression procedures, canonical correlation, structural equation modeling and other advanced methods
IRB
Institutional review boards, mandated by the Common Rule (sub part A) from 45 code of federal regulations of the U.S. Dept. Of health and human services.
Minimal risk
Harm or discomfort can’t be greater than those encountered in daily life
Informed consent
Required for human subject research. Individual must be informed of the duration, procedures and point of the research; the risks and benefits; the manner of maintaining confidentiality or anonymity; any processes that involve more than minimal risk and procedures in case of injury; contact info for researcher and IRB; statement that participation is voluntary and participant can withdraw at any time
Assent
A child’s affirmative agreement to participate when legal consent is not possible
Conflicts of interest
Objectivity: researcher feelings, beliefs or attitudes incompatible with responsible and unbiased research
Benefit: researchers receive some type of welfare, service or profit for engaging in research
Not a dealbreaker but just be addressed
Vulnerable populations
Children, prisoners, pregnant women, mentally disabled persons, economically or educationally disadvantaged persons.
IRBs concerned with coercion and assent (and for children), and representation (by the institution in question, on the IRB). Requires additional provisions to protect, so document protocol, risks and benefits
Unanticipated problems
IRB requires written procedures for dealing with them and reporting promptly to IRB. OHRP distinguishes these from adverse effects.
Adverse events
Physical or psychological harm. Need to be reported if unanticipated, only if it happens as a result of participation. Might result in revised protocols, suspension, termination of study.
ACA code of ethics, section G
Expands on the common rule. Subsections for:
Research responsibilities, rights of participants, managing and maintaining boundaries, reporting results, publications and presentations
IRB protocol
Research project should be worthwhile.
Provide the following info:
Description of research
Participants
Risks and benefits
Informed consent
Confidentiality or anonymity and data security
Methods and measures
Generalizability
Can findings be attributed to larger population