Terms Flashcards
Nursing Research
A systematic process of inquiry that uses rigorous guidelines to produce unbiased, trustworthy answers to questions about nursing practice.
Peer Review
The process of subjecting research to the appraisal of a neutral third party. Common processes of peer review include selecting research for conferences and evaluating research manuscripts for publication.
Blinded
A type of review in which the peer reviewer is unaware of the author’s identity, so personal influence is avoided.
Replication
Repeating a specific study in detail on a different sample. When a study has been replicated several times and similar results are found, the evidence can be used with more confidence.
Magnet Status
A designation for organizations that have characteristics that make them attractive to nurses as workplaces.
National Institute of Nursing Research (NINR)
A federal agency responsible for the support of nursing research by establishing a national research agenda, funding grants and research awards, and providing training.
Journal Club
A formally organized group that meets periodically to share and critique contemporary research in nursing, with a goal of both learning about the research process and finding evidence for practice.
Systematic Review
A highly structured and controlled search of the available literature that minimizes the potential for bias and produces a practice recommendation as an outcome.
Evidence-based Practice Guideline:
A guide for nursing practice that is the outcome of an unbiased, exhaustive review of the research literature, combined with clinical expert opinion and evaluation of patient preferences. It is generally developed by a team of experts.
Principal Investigator
The individual who is primarily responsible for a research study. The principal investigator is responsible for all elements of the study and is the first author listed on publications or presentations.
Quality Improvement
The systematic, data-based monitoring and evaluation of organizational processes with the end goal of continuous improvement. The goal of data collection is internal application rather than external generalization.
Outcomes Measurement
Measurement of the end result of nursing care or other interventions; stated in terms of effects on patients’ physiological condition, satisfaction, or psychosocial health.
Nursing Process
A systematic process used by nurses to identify and address patient problems; includes the stages of assessment, planning, intervention, and evaluation.
Evidence-based Practice
The use of the best scientific evidence, integrated with clinical experience and incorporating patient values and preferences in the practice of professional nursing care.
Randomized Controlled Trial
An experiment in which subjects are randomly assigned to groups, one of which receives an experimental treatment while another serves as a control group. The experiment has high internal validity, so the researcher can draw conclusions regarding the effects of treatments.
External Validity
The ability to generalize the findings from a research study to other populations, places, and situations.
Paradigm
An overall belief system or way of viewing the nature of reality and the basis of knowledge.
Quantitative Research
A traditional approach to research in which variables are identified and measured in a reliable and valid way.
Qualitative Research
A naturalistic approach to research in which the focus is on understanding the meaning of an experience from the individual’s perspective.
Mixed Method
A research approach that combines quantitative and qualitative elements; it involves the description of the measurable state of a phenomenon and the individual’s subjective response to it.
Basic Research
Theoretical, pure, fundamental, or bench research done to advance knowledge in a given subject area.
Applied Research
Research conducted to gain knowledge that has a practical application and contributes in some way to a modification of practice.
Experimental Research
Highly structured studies of cause and effect, usually applied to determine the effectiveness of an intervention. Subjects are selected and randomly assigned to groups to represent the population of interest.
Quasi-experimental Studies
Studies of cause and effect similar to experimental design but using convenience samples or existing groups to test interventions.
Retrospective Studies
Studies conducted using data that have already been collected about events that have already happened. Such secondary data were originally collected for a purpose other than the current research.
Prospective Studies
Studies planned by the researcher for collection of primary data for the specific study and implemented in the future.
Longitudinal Studies
Studies conducted by following subjects over a period of time, with data collection occurring at prescribed intervals.
Cross-sectional Methods
Studies conducted by looking at a single phenomenon across multiple populations at a single point in time, with no intention for follow-up in the design.
Ethics
A type of philosophy that studies right and wrong.
Therapeutic Research
Studies in which the subject can be expected to receive a potentially beneficial treatment.
Nontherapeutic Research
Studies that are carried out for the purpose of generating knowledge. They are not expected to benefit the research subject, but may lead to improved treatment in the future.
Respect for Persons
A basic principle o ethics stating that individuals should be treated as autonomous beings who are capable of making their own decisions. Persons who have limited autonomy or who are not capable of making their own decisions should be protected.
Vulnerable Populations
Groups of people with diminished autonomy who cannot participate fully in consent process. Such groups may include children, individuals with cognitive disorders, prisoners, and pregnant women.
Beneficence
A basic principle of ethics that states that persons should have their decisions respected, be protected from harm, and have steps taken to ensure their well-being.
Justice
A basic principle of ethics that incorporates a participant’s right to fair treatment and fairness in distribution of benefit and burden.
Informed Consent
A process of information exchange in which participants are provided with understandable information needed to make a participation decision, full disclosure of the risks and benefits, and the assurance that withdrawal is possible at any time without consequences. This process begins with recruitment and ends with a signed agreement document.
Full Disclosure
Reporting as much information about the research as is known at the time without threatening the validity of the study. This practice allows the subject to make an informed decision as to whether to participate.
A Priori
Conceived or formulated before an investigation.