Glossary | National Collaborating Centre for Methods and Tools

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6S Pyramid

6S Pyramid

A guide for finding the best available research evidence quickly and efficiently. Each level of the pyramid draws on research evidence from the lower layers, therefore more synthesized evidence is found at the higher levels. It is recommended that searching for evidence begin at the top (or the highest possible level) of the pyramid.

DiCenso, A., Bayley, L., & Haynes, B. (2009). Accessing pre-appraised evidence: fine tuning the 5S model into a 6S model. Evidence-Based Nursing, 12(4), 99-101.

A

Absolute Risk Difference: The difference in the number of events (outcome) between intervention and control groups (obtained by subtracting number of events in the intervention group from the number of events in the control group); usually reported as a %. Also see: Absolute risk reduction.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

Absolute Risk Reduction: The difference in the number of events (outcome) in the control group minus the number of events (outcome) in the treatment group. For example, if the number of events (e.g. death) in the control group (not receiving the intervention) is 40 per 100 patients, while the number of events in the intervention group is 30 per 100 patients, absolute risk reduction = 0.40 – 0.30; absolute risk reduction = 0.10 or 10%. This means the intervention group has a 10% absolute lower risk of death than the control group.

Barratt, A., Wyer, P.C., Hatala, R., McGinn, T., Dans, A.L., Keitz, S., Moyer, V., Guyatt, G. (2004). Tips for learners of evidence-based medicine: 1. Relative risk reduction, absolute risk reduction and number needed to treat. CMAJ, 171(4), 353-358.

Centre for Evidence-Based Medicine, University of Oxford. (2005). Critical appraisal for therapy articles. Retrieved from https://www.cebm.ox.ac.uk/resources/ebm-tools/glossary

Allocation: A process by which participants are assigned to either the experimental (intervention) group or comparison/control group in a study. Random allocation is done by chance. Studies that allocate participants that do not use random allocation usually do so by having participants selected themselves or are selected by the researcher to receive the intervention.

Cullum, N., Ciliska, D., Haynes, R. B., & Marks, S. (2008). Evidence-Based Nursing: An Introduction. Oxford: Blackwell.

Allocation Concealment: The process of shielding those involved in the trial from knowing the upcoming participant group assignment.

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

Analytic Study

A study that explores the relationship between one or more factors on an outcome:

the effect of an intervention;
exposure.

To quantify the relationship, the rate of the outcome in the intervention/exposed and control/comparison groups are compared. An experimental study implies active involvement of the researcher, (ie. Researcher involved in allocating participants to groups) while an observational study implies passive involvement of researcher (e.g. participants self-select to receive an intervention).

Glasziou, P., & Heneghan, C. (2009) A spotter’s guide to study design. Evidence-Based Nursing, 12(3), 71-72.

Applicability: Applicability assesses the feasibility of providing an intervention in a local setting. Applicability considers cost-effectiveness, organizational culture and capacity.

Buffett, C., Ciliska, D., & Thomas, H. (2007). Can I use this evidence in my program decision? Assessing applicability and transferability of evidence. Hamilton, ON: National Collaborating Centre for Methods and Tools (NCCMT).

Appraise: The process of assessing the quality of study methods in order to determine if findings are trustworthy, meaningful and relevant to your situation.

National Collaborating Centre for Methods and Tools. (2016). Appraise: Critically and efficiently appraise the research sources. Retrieved from http://www.nccmt.ca/eiph/appraise-eng.html

B

Bias: A systematic error in the design, conduct, or interpretation of a study that may cause a difference from the truth. For example, selection bias can occur when the results of a study are distorted by the way in which the participants are chosen to take part.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

Blinding (masking): Occurs in an experimental study when patients, clinicians providing an intervention, people assessing outcomes, and/or those analyzing data are unaware of the group to which participants were assigned.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

Bracketing: Bracketing is a method to increase the rigor of the project by mitigating the potential effects of unacknowledged preconceptions related to the research. A close relationship may exist, or may develop during the process of qualitative research, between the researcher and the research topic. Bracketing protects the researcher from the cumulative effects of examining what may be emotionally challenging material.

Tufford, L., & Newman, P. (2012). Bracketing in Qualitative Research. Qualitative Social Work, 11(80), 80-96. doi: 10.1080/10503300902798375

C

Capacity Development: The development of knowledge, skills and attitudes among individuals and groups of people. Also involves the creation of structures, resources, policies and procedures in organizations and networks to sustain and achieve relevant goals, to cope with complexity and to innovate.

Robeson, P. (2009). Networking in Public Health: Exploring the Value of Networks to the National Collaborating Centres for Public Health. Hamilton, ON: National Collaborating Centre for Methods and Tools. Retrieved from http://www.nccmt.ca/pubs/NetworkingPaperApr09EN_WEB.pdf

Case-control Study: An observational study that begins by identifying participants who have the outcome of interest, e.g. disease (cases) and participants who are similar to cases who do not have the outcome of interest (controls) and then looking back in time to see whether participants in both groups were exposed to risk factors or causal factors associated with the outcome. For example, identifying patients with (cases) and without (controls) lung cancer and looking back in time to determine past smoking behaviour (exposure to tobacco).

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

Case Report: A study reporting observations on a single individual.

Schünemann, H., Brożek, J., Guyatt, G., Oxman, A. (2013). GRADE Handbook. Retrieved from https://gdt.gradepro.org/app/handbook/handbook.html.

Case Series: A report on a series of patients with an outcome of interest, or receiving the same intervention, with no comparison group.

Schünemann, H., Brożek, J., Guyatt, G., Oxman, A. (2013). GRADE Handbook. Retrieved from https://gdt.gradepro.org/app/handbook/handbook.html.

Case Study: The study of selected current phenomenon over time to provide an in-depth description of essential dimensions and processes of the phenomenon. Case studies may involve both qualitative and quantitative data and may focus on single or multiple cases.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

LoBiondo-Wood, G., & Haber, J. (2002). Nursing research: Methods, critical appraisal and utilization (5^th ed.). St. Louis: Mosby.

Causation: Studies that consider risk factors (exposure) for certain diseases/problems/conditions (outcomes), e.g. the effect of patient characteristics (exposure) on the development of pressure ulcers (outcome). Also referred to as “etiology” or “aetiology”.

Adamson, J. (2004). Evaluation of studies of causation (etiology). Evidence-Based Nursing, 7¸ 36-40.

Clinical Significance: Assesses whether the size of the effect of an intervention is big enough to justify the investment required for its implementation. Assessing clinical significance takes into account factors such as the size of a treatment effect, the importance of the problem being addressed, the other potential outcomes of the intervention, and the cost of implementation.

Schünemann, H., Brożek, J., Guyatt, G., Oxman, A. (2013). GRADE Handbook. Retrieved from https://gdt.gradepro.org/app/handbook/handbook.html.

Cochrane Collaboration

An international non-profit organization of volunteers who conduct systematic reviews on a variety of health topics. www.cochrane.org

Of particular interest, there is a review group for public health (http://ph.cochrane.org/cph-reviews-and-topics) and for implementation of evidence (The Effective Practice and Organization of Care Review Group, http://epoc.cochrane.org/).

Cohort: A group of individuals who are linked in some way or who have experienced the same significant life event within a given period (e.g. birth year, or exposure to a particular drug).

Cohort Study: A study in which a group of people with a common set of characteristics or a set of characteristics are followed up for a period of time to determine the incidence of an outcome.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

Collaboration: A process of interaction where actors work together to achieve desired outcomes.

Community of Practice: Voluntary, flexible networks of people with a common interest who learn about, share knowledge and develop expertise on an issue.

Robeson, P. (2009). Networking in Public Health: Exploring the Value of Networks to the National Collaborating Centres for Public Health. Hamilton, ON: National Collaborating Centre for Methods and Tools. Retrieved from http://www.nccmt.ca/pubs/NetworkingPaperApr09EN_WEB.pdf

Comparison Group: Participants in a study who receive the standard of care or conventional therapy/treatment instead of the experimental therapy/treatment (intervention).

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

Confidence Interval: Provides the likely range of the true value of interest (e.g. the effect of an intervention or treatment). The confidence interval is usually reported as ‘95% confidence interval’, which means that 95% of the time the true value (effect) for the population lies within the given range of values.

BMJ Publishing Group Ltd and RCN Publishing Company Ltd. (2009). Glossary. Evidence-Based Nursing, 128(4), doi:10.1136/ebn.12.4.128-b

Confirmability: A component of qualitative validity, confirmability refers to the degree to which the results could be confirmed or corroborated by others.

Trochim, W.M. (2006). Research Methods Knowledge Base: Qualitative Validity. Retrieved from http://www.socialresearchmethods.net/kb/qualval.php

Confounder: A factor that is associated with both an intervention (or exposure) and the outcome of interest. For example, if people in the experimental group of a controlled trial are younger than those in the control group, it will be difficult to decide whether a lower risk of death in one group is due to the intervention or the difference in age. Age is then said to be a confounder, or a confounding variable. Confounding is a major concern in non-randomized studies, given there is greater chance that confounders will not be equally distributed among groups.

Schünemann, H., Brożek, J., Guyatt, G., Oxman, A. (2013). GRADE Handbook. Retrieved from https://gdt.gradepro.org/app/handbook/handbook.html.

Continuous Data: Data with a potentially infinite number of values along a continuum (weight, blood pressure, temperature).

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

Control Group: Participants in a study who receive no intervention and whose performance provides a baseline against which the effects of the treatment can be measured; when a study does not involve a true experimental design [randomized controlled trial (RCT)] this group may also be called the “comparison group”.

Polit, D. F., & Hungler, B. P. (1999). Nursing research: Principles and methods (6^th ed.). Philadelphia: Lippincott.

Credibility: A component of qualitative validity, credibility refers to the ability of a study to reveal the truth, and the probability that the study’s methods will produce plausible findings.

Russell, C. K., & Gregory, D. M. (2008). Evaluation of Qualitative Research Studies. In N. Cullum, D. Ciliska, R. B. Haynes & S. Marks (Eds.), Evidence-based nursing. An introduction (pp. 204-218). Oxford: Blackwell.

Critical Appraisal: The process of systematically examining research to judge its trustworthiness, and its value and relevance in a particular context.

Burls, A. (2015). What is critical appraisal? International Journal of Evidence-Based Practice for the Dental Hygienist,1, 80-85.

Cross-sectional Study: An observational study that examines a characteristic (or set of characteristics) and the outcome of interest in participants at one point in time. Sometimes referred to as a survey study.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

D

Data Extraction

The process of capturing information, in this case, about a knowledge translation method or tool to help the user decide if it is relevant to their needs. The Measurement and Descriptive Information (MADI) Tool was developed from a range of critical appraisal checklists to critically appraise the method or tool. The MADI Tool gathers the following information about the method or tool:

Content (sections of the resource, etc.)
Relevance for public health
Evaluation history and measurement (reliability, validity) characteristics
Development (how the resource was developed)
Access issues (cost, format, language)
Implementation issues (participants, time, resources needed)
Supplementary resources
Current contact person

For more information, see Registry Methodology.

Data Saturation: Data saturation occurs when research questions are comprehensively and completely answered, when participant interviews are no longer adding new information to the study finding, or when findings begin being repeated.

Russell, C. K., & Gregory, D. M. (2008). Evaluation of Qualitative Research Studies. In N. Cullum, D. Ciliska, R. B. Haynes & S. Marks (Eds.), Evidence-based nursing: An introduction (pp. 204-218). Oxford: Blackwell.

Dependability: A component of qualitative validity, dependability refers to the concept of consistency within a study, and whether the process of research is logical and clearly documented, particularly as it relates to the chosen method and decisions made by the researchers.

Russell, C. K., & Gregory, D. M. (2008). Evaluation of Qualitative Research Studies. In N. Cullum, D. Ciliska, R. B. Haynes & S. Marks (Eds.), Evidence-based nursing. An introduction (pp. 204-218). Oxford: Blackwell.

Descriptive Study

A study that describes characteristics of a sample of individuals. Unlike an experimental study, the investigators do not actively intervene to test a hypothesis, but rather describe the health status or characteristics of a sample from a defined population.

Descriptive studies include case reports, case-series, qualitative studies, and surveys (cross sectional studies).

Schünemann, H., Brożek, J., Guyatt, G., Oxman, A. (2013). GRADE Handbook. Retrieved from https://gdt.gradepro.org/app/handbook/handbook.html.

Glasziou, P., & Heneghan, C. (2009). A spotter’s guide to study design. Evidence-Based Nursing, 12(3), 71-72.

Diagnostic Study: A diagnostic study tests a new diagnostic method to see if it is as good as the ‘gold standard’ method of diagnosing a disease. The diagnostic method may be used when people are suspected of having a disease because of signs and symptoms, or to try and detect a disease before any symptoms have developed (a screening method).

National Institute for Health and Care Research. (n.d.). Glossary. Retrieved from https://evidence.nihr.ac.uk/glossary/

Dichotomous Data: Data that can take one of two values (eg, dead or alive, symptoms present or absent). Also known as binary data.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

Discussion Forum: An online space in which people can share knowledge about a common interest.

Organisation for Economic Co-operation and Development. (2012). Glossary. Retrieved from https://www.oecd-ilibrary.org/docserver/9789264055087-en.pdf?expires=1726774407&id=id&accname=guest&checksum=EDD2923D1FBAD7EBDDE8B5EE31CC1480.

Dissemination: The one-way spreading of knowledge or research, such as is done in scientific journals and at scientific conferences as well as extracting the main messages or key implications derived from research results and communicating them to a specific audience.

Scott, C. (2006). Knowledge use in the Calgary Health Region. Canadian Electronic Library. https://books.google.ca/books?id=DRbpzwEACAAJ

E

Effect Size: Effect size is a generic term for the estimate of the true value of the effect (i.e. the amount of change) from a given intervention compared to not receiving the treatment/intervention or receiving another intervention (DiCenso, 2001; Higgins & Green, 2009). Effect size may be expressed as a relative risk, odds ratio, relative risk reduction, etc

DiCenso, A. (2001). Clinically useful measures of the effects of treatment. Evidence Based Nursing, 4, 36-39.

Effectiveness: The measure of the ability of an intervention, project, program, or policy to do what it was intended to do: produce a specific desired result or effect that can be quantitatively measured.

European Observatory on Health Systems and Policies. Glossary.

Ethnographic Study (or Ethnography): A qualitative research method whereby the experience of a culture is studied. Data collection approaches include participant observation, in-depth interviews, and field work.

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

Evaluate: Efforts aimed at determining, as systematically and objectively as possible, the relevance, effectiveness and impact of health-related (and other) activities in relation to objectives. Evaluation may or may not involve taking into account the resources that have been used.

Public Health Agency of Canada. (2006). Glossary of terms relevant to the core competencies for public health, E-H. Retrieved from http://www.phac-aspc.gc.ca/php-psp/ccph-cesp/glos-eng.php.

Rychetnik, L., Hawe, P., Waters, E., Barratt, A., & Frommer, M. (2004). A glossary for evidence based public health. Journal of Epidemiology and Community Health, 58, 538-545.

Evidence: Information or facts from a variety of both qualitative and quantitative sources, that are systematically obtained, i.e. obtained in a way that is replicable, observable, credible, verifiable, or basically supportable.

Adapted from Rycroft-Malone, J., & Stetler, C.B. (2004). Commentary on evidence, research, knowledge: a call for conceptual clarity. Worldviews on Evidence-Based Nursing, 1(2), 98-101.

Evidence-based Medicine: The conscientious, explicit and judicious use of the current best evidence in making decisions about the care of individual patients.

Sackett, D.L., Rosenberg, W.M., Muir-Gray, J.A., Haynes, R.B., & Richardson, W.S. (1996). Evidence-based medicine: what it is and what it isn’t. BMJ, 328, 535-536.

Evidence-informed Decision Making

Recognizes that important evidence comes from a variety of sources: community health issues and local context; public health resources; community and political climate; and the best available research findings. Decision makers must draw on their explicit and tacit public health knowledge and expertise to incorporate all the relevant factors into the final decision, conclusion or recommendation.

This model is particularly relevant for decision making in the fifth step of evidence-informed public health: Adapt the information to a local context.

Evidence-Informed Decision Making was formerly called Evidence-Based Decision Making.

National Collaborating Centre for Methods and Tools. (2009). A Model for Evidence-Informed Decision-Making in Public Health. [fact sheet]. Retrieved from http://www.nccmt.ca/pubs/FactSheet_EIDM_EN_WEB.pdf.

Evidence-informed Public Health: Put simply, it means finding, using and sharing what works in public health and involves seven steps: define, search, appraise, synthesize, adapt, implement, and evaluate.

National Collaborating Centre for Methods and Tools. (2016). Evidence-Informed Public Health. Retrieved from http://www.nccmt.ca/eiph/index-eng.html

Experimental Group: Participants in a study who receive the experimental therapy/treatment or intervention.

Polit, D. F., & Hungler, B. P. (1999). Nursing research: Principles and methods (6^th ed.). Philadelphia: Lippincott.

Experimental Study: A research design, most often a randomized controlled trial, that sorts study participants into two or more groups, with a minimum of one control group, the other(s) being the intervention group(s).Groups are then followed to assess whether or not an intervention (e.g. test, or treatment) that is controlled by the investigator, affects the course or outcome of a condition or disease. Experimental studies (rather than observational studies) are the preferred choice for most medical studies because control groups help minimize bias.

National Institute for Health and Clinical Excellence. (2010). Glossary. Retrieved from http://www.nice.org.uk/website/glossary/

BMJ Publishing Group. (2011). Clinical evidence: Glossary. Retrieved from https://bestpractice.bmj.com/info/toolkit/ebm-toolbox/a-glossary-of-ebm-terms/.

Explicit Knowledge: Knowledge that is available in spoken or written form; data and information that are arranged according to well-defined, formalized procedures or rules.

Adapted from NHS Evidence. Glossary of Health Knowledge Management Terms. Retrieved from http://webarchive.nationalarchives.gov.uk/20090518092537/http://www.library.nhs.uk/knowledgemanagement/Page.aspx?pagename=GLOSSARY

Exposure: Contact with something that influences the development of an outcome or improves the outcome for a person (e.g., exposure to something that causes an increased risk for developing a disease or, in people who already have the disease, reaching a particular endpoint).

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

F

Forum: An online grouping of related threads of discussion for people with common interests.

Fundamental Qualitative Description: Fundamental qualitative description is a purely descriptive research design with less interpretation than might be found in other qualitative descriptive studies such as phenomenological, grounded theory, or ethnographic.

Sandelowski, M. (2000). Focus on research methods: What happened to qualitative description? Research in Nursing & Health, 23, 334-340.

G

Grounded Theory: A qualitative research approach used to discover the social-psychological processes inherent in a phenomenon.

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

Guideline: Public health guidelines are recommendations for populations and individuals on activities, policies and strategies that can help prevent disease or improve health. The guidance may focus on a particular topic (e.g. cancer), a particular population (e.g. seniors) or a particular setting (e.g. home). They are based on the best available evidence. While guidelines help health professionals in their work, they do not replace their knowledge and skills. (See summaries in 6S Pyramid)

National Institute for Health and Clinical Excellence. (2010). Glossary. Retrieved from http://www.nice.org.uk/website/glossary/.

H

Harm: Adverse consequences of exposure to a stimulus.

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

Health Promotion: The comprehensive social and political process of enabling people to increase control over and improve their health through actions aimed at strengthening individual awareness and skill; changing individual behaviour; and changing social, organizational, political, and economic conditions that support good health practices.

O’Donnell, M.P. (1989). Definition of health promotion: Part III, expanding the definition. American Journal of Health Promotion, 3(5).

World Health Organization. (1998). Health promotion glossary. Retrieved from https://iris.who.int/bitstream/handle/10665/350161/9789240038349-eng.pdf?sequence=1.

Stanhope, M., & Lancaster, J. (1996). Community health nursing: Promoting health of aggregates, families, and individuals. Toronto: Mosby.

Heterogeneity Tests: Heterogeneity tests measure the extent of differences (i.e. heterogeneity) between individual studies. A significant test of heterogeneity suggests that the observed differences between individual study results are not the result of chance alone: another factor (e.g. study design, population) is responsible for the differences in treatment/intervention effects across studies. The results of these tests often help review authors decide whether it is appropriate to perform statistical synthesis (i.e. conduct a meta-analysis). Examples of heterogeneity tests include Cochran's Q, and the I² test of heterogeneity.

National Institute for Health and Clinical Excellence. (2010). Glossary. Retrieved from http://www.nice.org.uk/website/glossary/.

Homogeneous Sampling: A sampling method used in qualitative research whereby researchers decide at the beginning of the study to select participants who can provide similar stories or narratives on a phenomenon. Often selection is based on shared demographics or characteristics.

Thompson, C. (2008). If you could just provide me with a sample: Examining sampling in quantitative and qualitative research. In N. Cullum, D. Ciliska, R. B. Haynes & S. Marks (Eds.), Evidence-based nursing: An introduction (pp. 58-66). Oxford: Blackwell.

I

I2 Test of Heterogeneity: The I² test of heterogeneity describes the percentage of total variation across studies due to heterogeneity rather than chance. An I² value of 0% indicates no heterogeneity. In general, an I² value of 25% reflects low heterogeneity, 50% moderate heterogeneity, and 75% high heterogeneity. The I² can be calculated from a variety of study designs and types of outcome data. It is effective at detecting true heterogeneity between a small number of studies. I² = 100%x(Q – df)/Q (where Q is Cochran's Q and df the degrees of freedom).

Higgins, J.P.T., Thompson, S.G., Deeks, J.J., & Altman, D.G. (2003). Measuring inconsistency in meta-analysis. British Medical Journal, 327, 557-560.

Incidence: The number of new occurrences of something in the total population during a certain period. For example, the number of new cases of a disease in a country over one year. (See prevalence)

Law, K., & Howick, J. (2011). Centre for Evidence Based Medicine: Glossary. Retrieved from https://www.cebm.ox.ac.uk/resources/ebm-tools/glossary.

National Institute for Health and Clinical Excellence. (2010). Glossary. Retrieved from http://www.nice.org.uk/website/glossary/.

Inclusion Screening for National Collaborating Centre for Methods and Tools' Registry of Methods and Tools

A process used to assess resources generated by a search strategy to determine which should be included in National Collaborating Centre for Methods and Tools' Registry of Methods and Tools. We use three inclusion criteria to determine appropriate resources for the Registry:

The resource must contain a method and/or tool.
The method/tool must be used for one of the four types of knowledge translation activities.
The resource must be relevant to/adaptable for use in public health contexts.

The Inclusion Screening tool guides this process.

For more information, see Registry Methodology.

Integrated knowledge translation: Involves engaging and integrating those who will need to act on the findings, the knowledge users, into the research process.

Canadian Institutes for Health Research. (2012). Guide to Knowledge Translation Planning at CIHR: Integrated and End-of-Grant Approaches. Retrieved from www.cihr-irsc.gc.ca/e/45321.html

Intention-to-treat Analysis: All patients are analyzed in the groups to which they were randomized, even if they failed to receive/complete the intervention. Intention-to-treat analysis helps prevent bias caused by the loss of participants, and the resulting imbalance between comparison groups.

BMJ Publishing Group Ltd and RCN Publishing Company Ltd. (2009). Glossary. Evidence-Based Nursing, 128(4), doi:10.1136/ebn.12.4.128-b

Schünemann, H., Brożek, J., Guyatt, G., Oxman, A. (2013). GRADE Handbook. Retrieved from https://gdt.gradepro.org/app/handbook/handbook.html.

Interpretive Description: Also known as Qualitative Description, this is a qualitative research design that describes a phenomenon. Interpretive description is the foundation of all qualitative research designs.

Russell, C. K., & Gregory, D. M. (2008). Evaluation of Qualitative Research Studies. In N. Cullum, D. Ciliska, R. B. Haynes & S. Marks (Eds.), Evidence-based nursing: An introduction (pp. 204-218). Oxford: Blackwell.

Intervention: The aspect of interest in experimental and observational studies. Interventions can be therapeutic (e.g. different wound dressings), preventative (e.g. influenza vaccination), and diagnostic (e.g. measurement of blood pressure), targeted at individuals, groups, organizations, communities or health systems.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

K

Key Informants: Within the context of qualitative research, key informant refers to the person who is interviewed about a particular organization, social program, or problem. The key informant serves as a proxy for her or his associates within an organization or group. Key informant interviews are in-depth interviews of a select (non-random) group of experts who are most knowledgeable of the organization or issue.

Parsons, J. (2008). Key Informant. In P. Lavrakas (Ed.), Encyclopedia of Survey Research Methods. (p. 407). Thousand Oaks, CA: Sage Publications.

Knowledge: The capacity for effective action that results from information, including familiarity, awareness and understanding gained through experience or study. It results from making comparisons, identifying consequences and making connections.

Adapted from NHS Evidence. Glossary of Health Knowledge Management Terms. Retrieved from http://webarchive.nationalarchives.gov.uk/20090518092537/http://www.library.nhs.uk/knowledgemanagement/Page.aspx?pagename=GLOSSARY

Knowledge Application: Results in putting knowledge into action in practice settings or circumstances, including adoption, uptake, use and mobilization. It is also important to figure out how to use evidence appropriately and effectively within the local context. For example, developing a protocol to support a new program is an application activity.

Canadian Institutes of Health Research. About Knowledge Translation

Knowledge Broker

An individual or organization that aims to develop relationships and networks with, among, and between producers and users of research evidence and knowledge in order to facilitate:

a) knowledge exchange and co-development,
b) the appropriate use of the best available evidence in decision-making processes, and
c) individual and organizational capacity to participate effectively in the evidence-informed decision making process.

Knowledge Dissemination: The process of pushing out or distributing information, including research evidence, and adapting the content and the means for delivery to appropriate for the intended audience(s). Activities and tools include briefing documents, educational sessions or workshops, online reviews, summary statements and publications.

Canadian Health Services Research Foundation. Glossary of knowledge exchange terms as used by the Foundation.

Knowledge Exchange (formerly knowledge transfer): Collaborative problem-solving between researchers and decision makers that happens through linkage and exchange. Effective knowledge exchange involves interaction between decision makers and researchers and results in mutual learning through the process of planning, producing, disseminating, and applying existing or new research in decision making.

Canadian Health Services Research Foundation. (2012). Glossary of Knowledge Exchange Terms Used by the Foundation.

Knowledge Management

The systematic application of policies, methods and tools to create, capture, share and leverage the knowledge needed for an organization to succeed.

“The purpose of knowledge management is to provide support for improved decision making and innovation throughout the organization. This is achieved through the effective management of human intuition and experience augmented by the provision of information, processes and technology together with training and mentoring programmes.”

Clemmons Rumizen, M. (2002). The complete idiot's guide to knowledge management. Indianapolis, IN: Alpha Books.

D Snowden. (2009). Defining KM [Web log comment].

Knowledge Synthesis: A process of assessing current research evidence and expert opinion and providing a more comprehensive perspective on a specific topic. Syntheses identify gaps in evidence to help establish future research priorities and provide information to support policy and program decision making. The components are: identifying a question/problem of interest; establishing criteria to inform study selection; searching literature for relevant research; appraising studies critically; combining study results statistically/thematically; and summarizing synthesis findings.

Knowledge Translation: A systematic process for sharing knowledge between researchers and research users, including the synthesis, dissemination, exchange and ethically sound application of knowledge. The goal is to improve the health of Canadians, provide more effective health services and products and strengthen the health care system.

Adapted from Canadian Institutes for Health Research. (2016) About Knowledge Translation. Retrieved from http://www.cihr-irsc.gc.ca/e/29418.html

Other related terms include knowledge exchange, knowledge transfer, and many others. See also:

Canadian Institutes for Health Research. (2012). Guide to Knowledge Translation Planning at CIHR: Integrated and End-of-Grant Approaches. Retrieved from http://www.cihr-irsc.gc.ca/e/45321.html

L

Longitudinal: A study that examine changes in the same participants over time.

Burns, N., & Grove, S. K. (2001). The practice of nursing research: Conduct, critique, & utilization (4^th ed.). Philadelphia: W.B. Saunders.

M

Maximum Variation Sampling: A sampling method used in qualitative research whereby researchers select participants who can provide different narratives or accounts of experiencing a phenomenon. Often times, selection is based on differences in demographics or characteristics. Also known as heterogeneous sampling.

Thompson, C. (2008). If you could just provide me with a sample: Examining sampling in quantitative and qualitative research. In N. Cullum, D. Ciliska, R. B. Haynes & S. Marks (Eds.), Evidence-based nursing: An introduction (pp. 58-66). Oxford: Blackwell.

Mean: A value calculated by adding each value in a set of numbers/observations and dividing by the total number of observations. The mean is commonly called the ‘average.’

Schünemann, H., Brożek, J., Guyatt, G., Oxman, A. (2013). GRADE Handbook. Retrieved from https://gdt.gradepro.org/app/handbook/handbook.html.

Median: The median is the value in the middle of a data set, meaning that 50% of data points have a value smaller or equal to the median and 50% of data points have a value higher or equal to the median. For example, given the set of numbers 1, 3, 6, 8, 9 the median is 6.

Statistics Canada. (2021). 4.4.2 Calculating the Median. Retrieved from https://www150.statcan.gc.ca/n1/edu/power-pouvoir/ch11/median-mediane/5214872-eng.htm.

Meta-analyses: A method for combining the results of several independent studies that measure the same outcomes resulting in one overall summary statistic.

Dawson-Saunders, B., Trapp, R.G. (1994). Basic and Clinical Biostatistics. Norwalk: Appleton & Lange.

Methods: National Collaborating Centre for Methods and Tools uses this term to describe standardized processes, approaches or steps that facilitate access to and use of information for knowledge translation and decision making (e.g., a framework to create a dissemination plan).

Robeson, P. (2009). Networking in Public Health: Exploring the Value of Networks to the National Collaborating Centres for Public Health. Hamilton, ON: National Collaborating Centre for Methods and Tools. Retrieved from http://www.nccmt.ca/pubs/NetworkingPaperApr09EN_WEB.pdf

Mixed Methods Research: Research that combines data collection approaches, sometimes both qualitative and quantitative, into the study methodology, and is commonly used in the study of service delivery and organization. Some mixed method studies combine study designs, whereas others may have a single overarching research design, but use mixed methods for data collection.

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

Morbidity: Occurrence of an illness or illnesses in a population.

Friis, R. H., & Sellers, T. A. (2009). Epidemiology for public health practice (4^th ed.). Boston: Jones and Bartlett.

Mortality: Occurrence of death in a population.

Friis, R. H., & Sellers, T. A. (2009). Epidemiology for public health practice (4^th ed.). Boston: Jones and Bartlett.

N

Network: A system of interconnected individuals, groups or organizations as well as the links between them.

Robeson, P. (2009). Networking in Public Health: Exploring the Value of Networks to the National Collaborating Centres for Public Health. Hamilton, ON: National Collaborating Centre for Methods and Tools. Retrieved from http://www.nccmt.ca/pubs/NetworkingPaperApr09EN_WEB.pdf

Non-experimental Study (see Observational Study)

Non-Randomized Studies of Interventions: A study design in which participants who do not have the outcome of interest are allocated (but not randomly) to receive alternative treatment/therapy/interventions (experimental group) or the standard of care or conventional treatment (comparison group) or no intervention (control group) and then followed up to determine whether they experience the outcome of interest.

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

Number Needed to Treat: Is the number of patients who must be treated to prevent 1 additional negative event (or to promote 1 additional positive event). This is calculated as 1/absolute risk reduction (rounded to the next whole number), accompanied by the 95% confidence interval. When assessing clinical significance, one must consider the number needed to treat against any harms or adverse effects.

BMJ Publishing Group Ltd and RCN Publishing Company Ltd. (2009). Glossary. Evidence-Based Nursing, 128(4), doi:10.1136/ebn.12.4.128-b

Buckingham, J., Fisher, B., & Saunders, D. (2008). Evidence based medicine toolkit: Glossaries – clinical epidemiology. Retrieved from http://www.ebm.med.ualberta.ca/Glossary.html

O

Observational Study: A research design that requires investigators do not intervene or control variables rather, they observe the course of events. Changes or differences in one characteristic (e.g. whether or not people received the intervention of interest) are studied in relation to changes or differences in other characteristic(s) (e.g. death), without action by the investigator. There is a greater risk of bias in observational studies than in experimental studies. (Also known as non-experimental study).

Schünemann, H., Brożek, J., Guyatt, G., Oxman, A. (2013). GRADE Handbook. Retrieved from https://gdt.gradepro.org/app/handbook/handbook.html.

Odds Ratio: Describes the odds of a patient in the experimental group having an event divided by the odds of a patient in the control group having the event; or the odds that a patient was exposed to a given risk factor divided by the odds that a control patient was exposed to the risk factor.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell

Ordinal Data: An ordinal variable is a variable whose values are defined by an order relation between the different categories. For example, pain scale of “none/mild/moderate/severe”. Generally, short scales (e.g. a 1-5 pain scale) are analyzed as ordinal data.

Statistics Canada. (2021). Types of variables. Retrieved from https://www150.statcan.gc.ca/n1/edu/power-pouvoir/ch8/5214817-eng.htm.

Orientation: A typical pattern of activities and connections through which members experience being a network, such as meetings, open-ended conversations, projects, content, access to expertise, relationships, individual participation, community cultivation and serving a context.

Outcome (or Dependent Variable): The target variable of interest that is hypothesized to depend on or be caused by another variable (the independent variable).

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

P

P-value: A statistical value, which relates to the probability that the obtained results are due to chance alone; a p value of < 0.05 means that there is less than a 1 in 20 probability that the result occurred by chance alone.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

Participant: An individual who participates and provides information in a study; also called a “subject” of a study.

Polit, D. F., & Hungler, B. P. (1997). Essentials of nursing research: Methods, appraisal and utilization. Philadelphia: Lippincott.

Participatory Action Research

A qualitative research methodology which can be defined by five characteristics that distinguish it from other qualitative research methods:

1) Involves participation by the people involved in the research at all stages of the research process.

2) Values ways of knowing as theory is generated from the experiences, lives and understandings of all participants.

3) Focuses on empowerment and power relations in participatory research. People’s awareness of their own capabilities and capacity is strengthened by their participation in the research process.

4) Views consciousness-raising as the core of this approach. The research process may be educational for both the researcher and the participants because together they generate data.

5) Aims to create social change, which addresses the inequality of power distribution, and to affect the lives of those who participate in the research (including the researcher) in ways that the participants see as being beneficial to their lives.

Participatory action research can involve any or all of the following approaches:

· Direct observation

· Story telling

· Case stories

· Group meetings

· Understanding context through presence

· Timeline and change analysis

· Shared presentations and analysis

· Contrast comparisons

· Assessment and understanding of stakeholder needs

Koch, T & Kralik, D. (2006). Participatory Action Research in Health Care. Australia: Blackwell.

Phenomenology: A qualitative study design that represents an approach to enquiry that emphasizes the complexity of human experience and the need to understand that experience holistically, as it is actually lived.

Polit, D.F., & Hungler, B.P. (1997). Essentials of Nursing Research: Methods, Appraisal and Utilization. Philadelphia: Lippincott.

Planning: The initial stage of knowledge translation, before the doing and evaluation stages. Planning methods and tools are used when thinking about how to frame, approach or organize knowledge translation activities. For example, a planning tool with a work plan and checklist for actions can be used to help prepare a dissemination strategy.

Point Estimate: The point estimate is the statistical best guess or estimate of the effect of an intervention or treatment (e.g. the true value of interest).

Population: An observable collection of people (or organizations) that share important characteristics; the total number of subjects from which to derive a study sample.

Kirch, W. (Ed). (2001). Population. In Encyclopedia of Public Health. (pp. 1116-1117). New York: Springer.

Pre-appraised Research Evidence: Research evidence that has been reviewed for methodological rigour, synthesized, and in some cases further summarized into key messages by an individual or group, for example synopses of systematic reviews (syntheses) or synopses of studies.

Ciliska D., Thomas H., & Buffett C. (2008). An introduction to evidence-based public health and a compendium of critical appraisal tools for public health practice. Hamilton, ON: National Collaborating Centre for Methods and Tools. Retrieved from http://www.nccmt.ca/pubs/2008_07_IntroEIPH_compendiumENG.pdf

Robeson, P., Dobbins, M., DeCorby, K., & Tirillis, D. (2010). Facilitating access to pre-processed research evidence in public health. BMC Public Health, 10, 95.

Pre-processed Research Evidence: Evidence that someone has synthesized and in some cases critically appraised and further summarized into key messages.

Robeson, P., Dobbins, M., DeCorby, K., & Tirillis, D. (2010). Facilitating access to pre-processed research evidence in public health. BMC Public Health, 10, 95.

Prevalence: The proportion of a population having a particular condition or characteristic. For example, the percentage of people in a city with a particular disease, or who smoke. (See incidence)

National Institute for Health and Clinical Excellence. (2010). Glossary. Retrieved from http://www.nice.org.uk/website/glossary/.

Prognostic Factor: Participant characteristics that give increased or decreased risk of a positive or adverse health outcome from a given disease.

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

Public Health: An organized activity or way of thinking designed to promote, protect, improve and/or restore the health of individuals, specific groups or the entire population. A combination of sciences, skills and values aimed at protecting and improving the health of all people. The term “public health” can describe a concept, a social institution, a set of scientific and professional disciplines and technologies and a form of practice. It is a way of thinking, a set of disciplines, an institution of society and a manner of practice. It has an increasing number and variety of specialized domains and it demands of its practitioners an increasing array of skills and expertise.

Adapted from the Public Health Agency of Canada. Glossary of Terms. Retrieved from http://www.phac-aspc.gc.ca/php-psp/ccph-cesp/glos-eng.php

Public Health Decision Makers: People who work in the public health field, ranging from frontline public health providers (e.g., public health nurses, environmental health inspectors, dental hygienists, health promoters, etc.) to administrators (e.g., medical officers of health, program managers) and policy makers in provincial and federal government.

Purposive Sampling: A sampling method used in qualitative research, whereby researchers consciously select a small number of participants that meet particular inclusion criteria covering a range of relevant perspectives.

Thompson, C. (2008). If you could just provide me with a sample: Examining sampling in quantitative and qualitative research. In N. Cullum, D. Ciliska, R. B. Haynes & S. Marks (Eds.), Evidence-based nursing: An introduction (pp. 58-66). Oxford: Blackwell.

Q

Qualitative Description (See Interpretive Description)

Qualitative Research: Research that aims to generate an understanding of complex, unquantifiable phenomena, such as people’s experiences or perceptions. A few examples of types of qualitative research include phenomenology, grounded theory, participatory action research, and ethnography.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

Quality Assessment: Quality assessment criteria are checklists or standards that are used to evaluate research evidence. These criteria can be applied to assess the value of a single study, or to assess several studies as part of the systematic review process. Quality assessment criteria address different variables, depending on the nature and purpose of the research, and the expectations and priorities of the reviewers. Criteria include: methodological rigour, levels of evidence, strength of evidence, magnitude, completeness, relevance, and criteria of causation.

Rychetnik, L., Hawe, P., Waters, E., Barratt, A., & Frommer, M. (2004). A glossary for evidence based public health. Journal of Epidemiology and Community Health, 58, 538-545.

Quantitative Research: The investigation of phenomena that lend themselves to test well-specified hypotheses through precise measurement and quantification of pre-determined variables that yield numbers sustainable for statistical analysis.

DiCenso, A., & Guyatt, G. (2005). Health care interventions. In DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

Quasi-Experimental Study: A research design that differs from experimental studies in that participants are not randomly assigned to groups, but the investigator still controls the intervention(s) (e.g. test, or treatment) received by at least one of the groups. This means a researcher can't draw conclusions about 'cause and effect'. This design is frequently used when it is not feasible, or not ethical, to conduct a randomized controlled trial.

National Institute for Health and Clinical Excellence. (2010). Glossary. Retrieved from http://www.nice.org.uk/website/glossary/.

R

Random Allocation (or randomization): Assignment of participants to groups (experimental or comparison/control) by chance. This ensures that all of the participants have an equal chance of being assigned to either group (experimental or comparison/control group) and ensures all groups are balanced with respect to known or unknown factors that may affect the outcome of interest.

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

Random Sampling: A method of selecting participants for a study that uses some type of random selection to ensure that different units of the population being sampled are equally likely to be selected. Also know as probability sampling.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

Randomized Controlled Trial: An experiment in which participants or populations who do not have the outcome of interest, are allocated by chance to receive an intervention (intervention group) or not (comparison or control group) and then followed up over time to determine if differences between groups occurs on the outcome of interest.

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

Waters, E., Doyle, J., Jackson, N., Howes, F., Brunton, G., & Oakley, A. (2006). Evaluating the effectiveness of public health interventions: The role and activities of the Cochrane Collaboration. Journal of Epidemiology and Community Health, 60, 285-289.

Regression Analysis: A statistical technique that describes and tests the relationship between a dependent variable and one or more explanatory variables.

Max Rady College of Medicine. (2011). Term: Regression Analysis. Retrieved from http://mchp-appserv.cpe.umanitoba.ca/viewDefinition.php?definitionID=104148.

Relative Benefit

The proportional increase in the rates of good outcomes between experimental and control participants; it is reported as a percentage (%).

Relative benefit is calculated by dividing the rate of the positive outcome in the experimental group minus the rate of the positive outcome in the control group by the rate of the positive outcome in the control group.

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

Relative risk: The proportion of patients experiencing an outcome in the treated (or exposed) group divided by the proportion experiencing the outcome in the control (or unexposed) group. It tells us the risk or probability of an event occurring in the intervention group compared to the control group.

For example, if the number of events (e.g. death) in the control group (e.g. receiving placebo) is 60 per 100 control group members, while the number of events in the treatment/intervention group is 15 per 100 intervention group members, relative risk = (15/100) / (60/100), relative risk = 0.25 or 25%. Treatment reduced the probability(risk) of an event to 25% of what it would have been without treatment. An alternative interpretation is the Relative Risk Reduction.

BMJ Publishing Group Ltd and RCN Publishing Company Ltd. (2009). Glossary. Evidence-Based Nursing, 128(4), doi:10.1136/ebn.12.4.128-b

Relevance: The applicability and appropriateness of information as it relates to a question or issue at hand.

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

Risk Factor: Patient characteristics associated with the development of a disease in the first place. Authors often distinguish between risk factors and prognostic factors. Prognostic factors are patient characteristics that give increased or decreased risk of a positive or adverse health outcome from a given disease.

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

S

Sample: A selected subset of the population. A sample may be random or non-random, and may be representative or non-representative.

Last, J. (2001). A Dictionary of Epidemiology (4th ed.). New York, NY: Oxford University Press.

Search Strategy: A strategy to gather relevant knowledge translation methods and tools. These resources are then screened to determine if they will be included in the Registry (see Inclusion Screening).

For more information, see Registry Methodology.

Situation: A sequence of events or a combination of circumstances (which impacts a given population).

Snowball Sampling

A sampling method used in qualitative research when no sampling frame exists or when access to individuals might be difficult because of cultural or social reasons.

Usually an initial respondent is asked if they know of any other potential participants who might be willing to speak with the researchers. Sometimes participants are asked if they would be willing to approach potential informants on behalf of the researchers.

Thompson, C. (2008). If you could just provide me with a sample: Examining sampling in quantitative and qualitative research. In N. Cullum, D. Ciliska, R. B. Haynes & S. Marks (Eds.), Evidence-based nursing: An introduction (pp. 58-66). Oxford: Blackwell.

Standard Deviation

A standard deviation is a measure of how dispersed the data is in relation to the mean. In other words, standard deviation (SD), measures the spread of data across a sample, so a large SD suggests data are spread out over a wide range of values.

For example, the average (i.e. mean) height of males in a given population is reported as 5'10" ± 3". In this case the SD is 3, so the range of height within 1 SD of the mean is 5’7” – 6’.

In any normal distribution, roughly two-thirds (actually, 68.2%) of the scores fall between -1 and +1 SD and 95.4% between -2 and +2 SD.

National Library of Medicine (n.d.). Common Terms and Equations: Standard Deviation. Retrieved from https://www.nlm.nih.gov/oet/ed/stats/02-900.html.

Standardized Mean Difference (SMD): The standardized mean difference is the difference between two normalized means – i.e. the mean values divided by an estimate of the within-group standard deviation. The standardized mean difference is used for comparison of data obtained at different scales.

For example, consider a trial evaluating an intervention to increase birth weight. The mean birth weights in intervention and control groups were 2700g and 2600g, respectively, with an average SD of 500g. SMD = (2700 - 2600)/500 = 0.2.

Statistics.com. (n.d.). Glossary. Retrieved from https://www.statistics.com/glossary/standardized-mean-difference/.

Statistical Significance: Indicates the extent to which results obtained in a study occurred by chance and the null hypothesis is rejected (meaning that there is a difference in outcome between the groups). When statistically significant, the probability of finding the result by chance falls below a specified level of probability (most often p<0.05).

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

Stratification: The division of a population into distinct subgroups based on the presence or absence of particular characteristics.

Abdelnour C, Agosta F, Bozzali M, Fougère B, Iwata A, Nilforooshan R, Takada LT, Viñuela F, Traber M. Perspectives and challenges in patient stratification in Alzheimer's disease. Alzheimers Res Ther. 2022 Aug 13;14(1):112. doi: 10.1186/s13195-022-01055-y. PMID: 35964143; PMCID: PMC9375274.

Studies (singular: study): Single original research investigations.

DiCenso, A., Bayley, L., & Haynes, B. (2009). Accessing pre-appraised evidence: fine tuning the 5S model into a 6S model. Evidence-based nursing, 12(4), 99-101.

Summary: A succinct description of a study or systematic review. Summaries briefly present to decision makers the full range of available evidence on a given health issue.

Haynes, B. (2007). Of studies, syntheses, synopses, summaries, and systems: The “5S’ evolution of information services for evidence-based healthcare decisions. Evidence-Based Nursing, 10, 6-7.

Summary Statement: NCCMT creates summary statements for all the resources in the Registry of Methods and Tools. Each Registry summary includes a plain-language description of the resource including information about its relevance to public health, how it was developed, how it can be used and whether (and how) it has been evaluated.

Summary Writing: The final step in producing a summary statement of a knowledge translation resource for the Registry. Information from the data extraction tool, the Measurement and Descriptive Information (MADI) Tool, is transferred to the Summary Writing Template to complete the writing process.

For more information, see Registry Methodology.

Survey Study: An observational study that examines a characteristic (or set of characteristics) and the outcome of interest in participants at one point in time. Sometimes referred to as a cross sectional study.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

Synopses of Studies (singular: Synopsis of a Study): Provides a brief, but often sufficiently detailed summary of a high-quality study that can inform clinical practice.

DiCenso, A., Bayley, L., & Haynes, B. (2009). Accessing pre-appraised evidence: fine tuning the 5S model into a 6S model. Evidence-Based Nursing, 12(4), 99-101.

Synopses of Syntheses (singular: Synopsis of a Synthesis): Summarizes the findings of a high-quality systematic review and is often accompanied by a commentary that addresses the methodological quality of the review and the clinical applicability of its findings.

DiCenso, A., Bayley, L., & Haynes, B. (2009). Accessing pre-appraised evidence: fine tuning the 5S model into a 6S model. Evidence-based nursing, 12(4), 99-101.

Synopses (singular: Synopsis): Brief descriptions of original articles and reviews such as those that appear in the evidence-based journals.

Haynes, R.B. (2007). Of studies, syntheses, synopses, summaries and systems: the “5S” evolution of information services for evidence-based healthcare decisions. Evidence-Based Nursing, 10, 6-7.

Syntheses (singular: Synthesis): A summary of all evidence that relates to a particular question; the question could be one of intervention effectiveness, causation, diagnosis or prognosis. There are many ways in which syntheses can be conducted (e.g. systematic reviews, meta-analyses, narrative, critical realist, interpretative). It is important to assess the rigor of syntheses using criteria relevant for the process used in doing the synthesis.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

Systematic Review: A review of a clearly formulated question that uses systematic and explicit methods to identify, select, and critically appraise relevant research, and to collect and analyze data from the studies that are included in the review. Statistical methods (meta-analysis) may or may not be used to analyze and summarize the results of the included studies. A systematic review differs from a traditional literature review in that a literature review describes and appraises previous work, but does not specify the methods by which the included studies were identified, selected, or evaluated.

Rychetnik, L., Hawe, P., Waters, E., Barratt, A., & Frommer, M. (2004). A glossary for evidence based public health. Journal of Epidemiology and Community Health, 58, 538-545.

Systems: Evidence-based clinical information systems that integrate and concisely summarize all relevant and important research evidence about a clinical problem and automatically link, through electronic medical records, a specific patient’s circumstances to the relevant information.

Cullum, N., Ciliska, D., Haynes, R.B., & Marks, S. (2008). Evidence-based nursing: An introduction. Oxford: Blackwell.

T

Tacit Knowledge: Knowledge that resides within people in an organization and is not formalized into written or documented forms; accessible only through conscious efforts.

Adapted from NHS Evidence. Glossary of Health Knowledge Management Terms. Retrieved from http://webarchive.nationalarchives.gov.uk/20090518092537/http://www.library.nhs.uk/knowledgemanagement/Page.aspx?pagename=GLOSSARY

Theoretical Sampling: A method of sampling practiced in theory research. Theoretical sampling refers to decisions made throughout the entire research process in which data sources are selected based on emerging study findings. The ultimate goal is to develop a theory that is grounded in the data and accounts for behavioral variation.

DiCenso, A., Guyatt, G., & Ciliska, D. (2005). Evidence-based nursing: A guide to clinical practice. St. Louis, MO: Elsevier Mosby.

Tools: NCCMT uses this term to describe standardized products such as instruments, surveys and checklists that facilitate access to and use of information for knowledge translation and decision making (e.g., a checklist for a dissemination plan).

Transferability: A component of qualitative validity, transferability refers to the degree to which the results of qualitative research can be generalized or transferred to other contexts or settings.

Russell, C. K., & Gregory, D. M. (2008). Evaluation of Qualitative Research Studies. In N. Cullum, D. Ciliska, R. B. Haynes & S. Marks (Eds.), Evidence-based nursing: An introduction (pp. 204-218). Oxford: Blackwell.

Triangulation: A component of qualitative analysis, whereby key findings are corroborated using multiple sources of information.

Powers, B. A. (2005). Generating evidence through qualitative research. Evidence-based practice in nursing & healthcare: A guide to best practice (pp. 283-298). Philadelphia, PA: Lippincott.

V

Validity: The degree to which a result (of a measurement or study) is likely to be true and free of bias (systematic errors).

Schünemann, H., Brożek, J., Guyatt, G., Oxman, A. (2013). GRADE Handbook. Retrieved from https://gdt.gradepro.org/app/handbook/handbook.html.

Variable: An attribute of a person or object that varies, that is, takes on different values (e.g. body temperature, age, heart rate).

Polit, D. F., & Hungler, B. P. (1999). Nursing Research: Principles and Methods (6th ed.). Philadelphia: Lippincott.