RESEARCH EXAM 2 VOCAB ONLY Flashcards
o Protection of participants’ confidentiality such that even the researcher cannot link individuals with the data they provided
ANONYMITY
o The affirmative agreement of member of a vulnerable group (children) to participate in a study
assent
o Provided a model for many guidelines adopted by disciplinary organizations in the United States
belmont report
o An ethical principle that seeks to maximize benefits for study participants, and prevent harm
beneficence
o Allows researchers to refuse to disclose information on study participants in any civil, criminal, administrative, or legislative proceeding
ϖ Certificate of Confidentiality
o The fundamental ethical principles established by a discipline or institution to guide researchers’ conduct in research with human (or animal) study participants
code of ethics
o Document signed by participants that includes information about the study purpose, specific expectations regarding participation, the voluntary nature of participation, and potential costs and benefits
consent form
o Is a pledge that any information participants provide will not be publicly reported in a manner that identifies them and will not be made accessible to others
confidentiality
o Sessions following data collection so that participants can ask questions or air complaints
debriefing
o A situation in which the rights of study participants are in direct conflict with requirements of a study
ethical dilemma
o Means that the researcher has fully described the study, the persons right to refuse participation, and possible risk and benefits
full disclosure
o The return of a completed questionnaire reflects the person’s voluntary consent to participate
implied consent
o Means that participants have adequate information about the study, comprehend the information, and have the power of free choice, enabling them to consent to or decline participation voluntarily
informed consent
o In the United States, a group of people affiliated with an institution who convene to review proposed and ongoing studies with respect to ethical considerations
institutional review board (IRB)
o Is a risk expected to be no greater than those ordinarily encountered in daily life or during routine tests or procedures
minimal risk
o Consent is continuously renegotiated – QUALITATIVE
process consent
o Is fabrication, falsification, or plagiarism in proposing, conducting, or reviewing research, or in reporting results
research misconduct
o Designed to evaluate whether the benefits of participating in a study are in line with the cost, be they financial, physical, emotional, or social
risk/benefit assessment
o Generous monetary incentive
stipend
o Special groups of people whose rights in studies need special protection because of their inability to provide meaningful informed consent or because their circumstances place them at higher than average risk of adverse effects (children, unconscious)
vulnerable population
o The framework in a study that has its roots in a specified conceptual model
conceptual framework
o A schematic representation of a theory or conceptual model that graphically represents key concepts and linkages among them
conceptual map
o Interrelated concepts or abstractions assembled together in a rational scheme by virtue of their relevance to a common theme – sometimes called conceptual framework
conceptual model
o A broad characterization that thoroughly accounts for a phenomenon
descriptive theory
o The conceptual underpinnings of a study (theoretical framework in a theory based study) or (conceptual framework in studies based on a specific conceptual model
framework
o A theory that focuses on a limited piece of reality or human experience, involving a selected number of concepts (theory of stress)
middle-range theory
o A symbolic representation of concepts or variables and interrelationships among them
model
o Or conceptual maps visually represent relationships among phenomena and are used in both QUALITATIVE and QUANTITATIVE
schematic model
o A framework where the study based on a theory
theoretical framework
o An abstract generalization that presents a systemic explanation about relationships among phenomena
theory
is what would happen to people if they were exposed to a causal influence & were simultaneously not exposed to it
counterfactual
treatment
intervention
involves observation of the outcome (mood) at two points in time: before & after the intervention.
pretest-posttest design
refers to a group of participants whose performance on an outcome variable is used to evaluate the performance of the experimental group
control group
the group getting the intervention
experimental group
the most basic experimental design involves randomizing people to different groups and then measuring the outcome. this design is sometimes called:
posttest-only design
pretest data AKA
baseline data
involves exposing people to more than one treatment.
crossover design
pseudointervention presumed to have no therapeutic value, which is also called an attention control condition
placebo
called trials without randomization in the medical literature.
quasi-experiments
quasi-experiements lack
randomization
a frequently used quasi-experimental design which involvs comparing two or more groups of people before & after implementing an intervention.
non equivalent control group pretest-posttest design
involves collecting data over an extended period of time, and introducing the treatment during that period
time-series design
when researchers do not intervene by controlling the independent variable, the study is called?
non-experimental
non experimental study AKA
observational
when researchers study the effect of a cause they cannot manipulate, they design ____ ____.
correlational studies.
examine RELATIONSHIPS between variables
correlational studies.
is an interrelationship or association between two variables, that is, a tendency for variation in one variable to be related to variation in another
correlation
observational studies with a cohort design start with what and end with what?
presumed cause & presumed effect
cohort aka
prospective design