Chapter 2 Notes (Nursing Research)

2.1 Research: What Is It?

  • Nursing integrates art and science. The art of nursing = caring, compassion, communication; the science of nursing = care grounded in rigorous scientific inquiry. The word science appears in a Bachelor of Science in Nursing; nurses generate new knowledge through research and apply it to practice.

  • Definitions:

    • science: \text{Knowledge derived from rigorous observation and experimentation to systematically study the physical world to test/develop theories}

    • research: \text{Systematic study that leads to new knowledge and/or solutions to problems or questions}

  • Replication and reliability: replication studies are repeated studies to obtain similar results; essential for confidence in findings.

  • Nursing research focuses on: persons, health, nursing, environment; studies patient outcomes, nurse attitudes, effectiveness of policies, and teaching strategies in nursing education.

  • Research contributes to theory development and refinement; foundational for evidence-based practice (EBP).

  • Distinguishing research from EBP:

    • Research = generate new knowledge or validate existing knowledge.

    • EBP = apply new knowledge to clinical practice to improve outcomes.

    • EBP questions arise in clinical care; research questions arise from gaps in literature; both involve data analysis but with different endpoints.

  • Types of Research (not mutually exclusive): descriptive, explanatory, predictive, causal; basic or applied; quantitative or qualitative.

  • Box 2-1: Steps of the Research Process (8 steps):

    1. Identify the research question.

    2. Conduct a review of the literature.

    3. Identify a theoretical framework.

    4. Select a research design.

    5. Implement the study.

    6. Analyze data.

    7. Draw conclusions.

    8. Disseminate findings.

  • Deliberate/systematic approach is essential; many discoveries fail when steps are skipped. Replication helps guard against error.

  • Four aims and example questions drive how studies are conducted: describe, explain, predict, and causality. Example: pain during chest tube removal (CTR) to illustrate these aims.

  • Basic vs applied research:

    • basic (bench) research: gain knowledge for knowledge’s sake; may take years to become practically applicable.

    • applied research: seeks knowledge to solve a clinical problem; findings have immediate practical application.

  • Quantitative vs qualitative research:

    • Quantitative: numbers, precise measurements, often tests hypotheses; designs include randomized controlled trials (RCTs), quasi-experimental, correlational, descriptive surveys; typically larger samples.

    • Qualitative: words, descriptions of meanings, multiple realities; methods include phenomenology, grounded theory, ethnography, historical; typically smaller samples.

  • Mixed methods: combine quantitative and qualitative data collection/evaluation in the same study.

  • Empirical evidence: verifiable by experience/observation/experimentation.

  • Critical thinking prompts (examples): root words: quantitative (quantity) vs qualitative (quality); deductive vs inductive reasoning.

  • Key terms to remember: mixed methods, empirical evidence, descriptive/explanatory/predictive aims, basic/applied, quantitative/qualitative.


2.1 Types of Research (deeper): Descriptive, Explanatory, Predictive, Causality; Basic vs Applied; Quantitative vs Qualitative

  • Descriptive: answers “What is it?”; provides accurate descriptions, often observational in natural settings.

  • Explanatory: answers “What is the relationship among the variables?”; identifies relationships among phenomena.

  • Predictive: answers “Is there a difference between groups?”; forecasts relationships or differences between groups; caution: prediction does not imply causation.

  • Causality: asks “Does A cause B?”; often uses random assignment to study interventions.

  • Basic vs Applied (revisited): basic focuses on knowledge for knowledge’s sake; applied aims to solve clinical problems with immediate practice implications.

  • Quantitative vs Qualitative (revisited): quantitative uses numbers; qualitative uses words; many studies use mixed methods.

  • Example in practice: Table 2-1 illustrates building knowledge about CTR pain across aims (Describe, Explain, Predict, Causal).


Box 2-1: Steps of the Research Process (summary)

  • 1. Identify the research question.

  • 2. Review the literature.

  • 3. Identify a theoretical framework.

  • 4. Select a research design.

  • 5. Implement the study.

  • 6. Analyze data.

  • 7. Draw conclusions.

  • 8. Disseminate findings.


Quantitative vs Qualitative: reasoning and designs (Table 2-2; Fig. 2-1)

  • Philosophical perspectives:

    • Quantitative: one reality, objectively viewed by the researcher.

    • Qualitative: multiple realities, subjective, context-dependent.

  • Type of reasoning:

    • Quantitative: primarily deductive (theory -> hunch -> data).

    • Qualitative: primarily inductive (data -> theory/generalization).

  • Role of researcher:

    • Quantitative: controlled, structured.

    • Qualitative: participative, ongoing engagement.

  • Strategies:

    • Quantitative: control/manipulation of variables; structured settings.

    • Qualitative: naturalistic; allow situations to unfold.

  • Data analysis:

    • Quantitative: analysis of numbers with statistical tests.

    • Qualitative: analysis of words to identify themes.

  • Sample sizes:

    • Quantitative: typically larger samples.

    • Qualitative: smaller numbers of participants.

  • Designs (examples):

    • Quantitative: randomized controlled trial (RCT), quasi-experimental, correlational, descriptive survey.

    • Qualitative: phenomenological, ethnographical, grounded theory, historical, etc.

  • Mixed methods: combine both approaches.

  • Note: A given study may be descriptive, applied, qualitative, etc., or combine more than one orientation.


2.1 Key Terms (selected)

  • abstract: The first section of a research article providing an overview of the study.

  • introduction: States the problem and purpose.

  • review of literature: Unbiased, comprehensive synthesis of relevant published studies.

  • theoretical framework: Links theory concepts to study variables; may be presented as a model/diagram.

  • methods section: Describes study design, sample, data collection; includes rationale for design choices.

  • results: Describes data analysis and sample characteristics; includes significant findings (quantitative) or themes (qualitative).

  • discussion: Interprets results; links to literature and theory; discusses limitations and implications.

  • references: Full citations for retrieved articles; enables reader to locate original sources.

  • basic distinction: Research vs EBP (educational/best-practice emphasis): research generates knowledge; EBP applies it to care.


Practical implications and examples

  • EBP depends on high-quality published research; nurses must read, evaluate, and apply findings in care.

  • Studies in CTR pain illustrate how descriptive, explanatory, predictive, and causal aims can be pursued within a single research program.

  • Understanding types of research helps nurses select appropriate designs to answer clinical questions and translate findings into practice.


2.2 How Has Nursing Evolved as a Science?

  • Central idea: Nursing is a cycle of scientific development—grand theories lead to research, dissemination, application to practice, and refinement of theory.

  • Cycle components (Figure 2-2): Theory → Research → Dissemination → Application → Refinement; social/political factors influence priorities and dissemination.

  • Key historical arc: nursing evolved from an art to a science, with the science embedded in evidence and policy to improve patient outcomes.

  • Box 2-2: Nursing Research Priorities (a sample list emerging in the 21st century):

    • Bioterrorism, Chronic illness, Cultural/ethnic considerations, End-of-life/palliative care, Genetics, Gerontology, Global warming, Healthcare delivery systems, Health promotion, Immigration, LGBTQ health issues, Management of pandemics/natural disasters, Mental health, Nursing informatics, Opioid epidemic, Patient outcomes/quality of care, Racial health disparities, Safe administration of medications, Symptom management, etc.

  • Doctor of Nursing Practice (DNP) as the recommended terminal practice degree for advancing leadership in EBP.

  • Globalization and technology drive nursing research diffusion and collaboration (e.g., expanded Sigma Theta Tau, international journals like IJR).

  • National databases and outcomes measures (e.g., NDNQI) support benchmarking and quality improvement.

  • Genetics and the Human Genome Project (completed 2003) integrated into nursing education and research priorities.

  • Nursing research agendas began focusing on access to care, diversity, patient outcomes, and health policy impacts (Healthy People initiatives).

  • Shifts in the 1960s–1980s emphasized clinical problems, outcomes, and grand theories (King, Henderson, Orem, Rogers, Roy); later, 1980s–1990s emphasized research utilization and later EBP.

  • Ethics evolution: Belmont Report (1979) identified core ethical principles; IRBs formalized protections; ethics education and policy matured (Nuremberg Code, Declaration of Helsinki).

  • Era milestones (highlights by era):

    • Before 1900: Florence Nightingale as a foundational nurse researcher; environment and infection control; Notes on Nursing (1859/1946).

    • 1900–1929: Education-focused nursing research; Goldmark Report (1923) highlighted education inadequacies; Yale/Nursing program development; first nursing journal (1900); ANA established (1912).

    • 1930–1949: Great Depression and WWII slowed diffusion to practice; hospital-based diploma programs; Brown Report (1948) urged university-based education; more descriptive morbidity/mortality focus.

    • 1950–1969: University-based education expands; funding for nursing research increases; growth of nursing research centers; shift to clinical problems and outcomes; early grand theories (Peplau, Henderson, King, Levine, Orem, Rogers, Roy).

    • 1970–1989: Increased focus on application of research (research utilization) and later evidence-based practice; more doctoral-prepared nurses; ethical oversight grows; IRBs emerge; CINL expands to CINIAL Health Literature; ethics and patient protection emphasis.

    • 1990–1999: Interdisciplinary research grows; NCNR elevated to NIH institute status; electronic databases (CINAHL online from 1995); Iowa and Stetler models for research utilization; EBP emerges from research utilization.

    • 2000–2009: Globalization accelerates knowledge sharing; emphasis on patient safety, NDNQI benchmarking; Human Genome Project influences genetics in nursing; rise of Doctor of Nursing Practice degree; EMR adoption begins; Magnet Recognition linked to evidence-based practice.

    • 2010–2019: EMR widespread; concerns about data security; telehealth expands; focus on patient outcomes, quality improvement, and linkages between EBP and EMRs; national data driving reimbursement decisions; Nurse workforce concerns (shortages, staffing ratios).

    • 2020–present: SARS-CoV-2 pandemic accelerates telehealth, infection prevention, and innovative care delivery; global collaboration; ongoing ethical concerns with digital data; renewed focus on workforce recruitment/retention and disparities; telehealth outcomes and access continue to be studied.


2.2 What Lies Ahead?

  • Continued drivers: social/political factors, patient safety/outcomes, technology, and globalization.

  • Priorities likely to persist, with emphasis on replication studies to confirm prior findings and on generating more middle-range and practice-oriented theories.

  • EBP will remain central to translating research into care, with educators tasked to train nurses in research literacy, evidence retrieval, critical appraisal, and implementation.

  • Interdisciplinary and international collaboration remains important (e.g., Joanna Briggs Institute).

  • Key topics for future nursing research (from Box 2-2): Bioterrorism; Chronic illness; Cultural and ethnic considerations; End-of-life/palliative care; Genetics; Gerontology; Global warming; Healthcare delivery systems; Health promotion; Immigration; LGBTQ health; Management of pandemics/natural disasters; Mental health; Nursing informatics; Opioid epidemic; Patient outcomes/quality of care; Racial health disparities; Safe administration of medications; Symptom management.

  • Practice implications: DNP as essential for leadership in EBP; magnet status linked to evidence-based practice; EMR integration with evidence-based guidelines.


2.3 What Lies Ahead? (Continued)

  • The Doctor of Nursing Practice (DNP) is the recommended educational requirement for advanced practice nursing; clinically prepared nurses can lead EBP.

  • Global collaborations (e.g., Joanna Briggs Institute) enable shared best practices across borders.

  • Emphasis on cultural, social, ethical, and technology-enabled health care delivery in future research agendas.

  • Test Your Knowledge 2-3 and 2-5 tasks reinforce synthesis of concepts and future-oriented thinking.


2.4 Keeping It Ethical

  • Objectives:

    • Identify five unethical studies and discuss international/national initiatives promoting ethical conduct.

    • Describe the rights of participants and the Belmont/Declaration-based principles guiding ethical research.

    • Explain the roles of IRBs and the composition/criteria for IRB membership.

    • Distinguish between vulnerable populations and non-vulnerable groups; differentiate full vs expedited vs exempt reviews.

    • Provide examples of research exempt from consent under certain conditions.

    • Differentiate between the research imperative (advancing knowledge) and the therapeutic imperative (patient care).

  • Nazi experiments (World War II) illustrate extreme violations; led to the Nuremberg Code establishing fundamental ethical rules.

  • Other historical unethical studies:

    • Tuskegee syphilis study (1932–1972): lack of informed consent; denial of penicillin when effective; increased harm.

    • Jewish Chronic Disease Hospital study (1960s): injection of cancer cells into debilitated patients without proper consent/awareness.

    • Willowbrook hepatitis studies (1960s): coercive participation; parents coerced for admission.

    • Red wine studies (2000s): data fabrication and falsification by a researcher; public distrust.

  • International and national guidelines:

    • Nuremberg Code: 10 key provisions emphasizing voluntary informed consent, minimize harm, scientific validity, and qualified researchers. See Box 2-3 for the complete list.

    • Declaration of Helsinki (1964, last amended 2013): physician guidelines for biomedical research; emphasizes informed consent and participant welfare.

    • Belmont Report (1979): three core principles foundational to ethical human participant research: Respect for Persons, Beneficence, Justice.

    • U.S. federal regulations (45 C.F.R. 46, last updated 2017): establish IRB requirements, protections for human subjects, and review processes.

    • ANA and Nursing organizations: ethical guidelines for nurses in research, including protecting rights (e.g., right to freedom from harm, privacy/dignity, anonymity).

  • Belmont Report principles explained:

    • Respect for Persons: autonomous individuals should be treated as such; those with diminished autonomy require protection; examples of past violations include Nazi experiments, Jewish Chronic Disease Hospital study, Willowbrook.

    • Beneficence: do no harm; maximize benefits, minimize risks; justify risks by anticipated benefits; Willowbrook and Tuskegee illustrate failures.

    • Justice: fair distribution of burdens and benefits; avoid exploiting vulnerable groups; ensure equitable selection of participants.

  • Institutional Review Boards (IRBs):

    • Primary mechanism for participant protection at organizational level; federal guidelines govern IRB composition and functioning.

    • IRB membership requirements (min 5 members; diverse expertise; at least one scientist, at least one non-scientist, and at least one unaffiliated member; community representation; avoid conflicts of interest).

    • Review types: full review (higher risk or vulnerable populations) vs expedited review (minimal risk).

    • Box 2-4: Key Code of Federal Regulations principles for IRB review (risk minimization, risk-benefit balance, equitable participant selection, informed consent requirements, privacy, monitoring, safeguards for vulnerable populations).

    • Box 2-5: Examples of exempt research (low-risk activities like educational tests with anonymity, research on existing datasets, certain public health program evaluations); exemptions do not automatically apply and IRB must review.

  • Exemptions and consent in practice:

    • Even exempt research requires IRB review; exemptions do not apply to prisoners, pregnant individuals, fetuses, newborns, or many children.

  • Therapeutic vs research imperatives in nursing:

    • In practice, patient rights and well-being trump research aims if conflicts arise; ethical decision-making requires balancing care with knowledge advancement.


2.4 Keeping It Ethical (Key Points and Practice Questions)

  • Examples of ethical questions and scenarios (critical thinking prompts) are provided throughout to reinforce ethical decision-making in research settings.

  • Sample test prompts include identification of ethical principles violated in hypothetical situations and how to respond as a nurse advocate.

  • IRB processes, risk/benefit assessment, informed consent documentation, and safeguarding privacy are core competencies for nursing researchers.


Box and Box-Like Content (Key References and Structures)

  • Box 2-1: Steps of the Research Process (see above).

  • Box 2-2: Nursing Research Priorities (topic areas for future work).

  • Box 2-3: Articles of the Nuremberg Code (10 points) – voluntary informed consent, risk-benefit balance, qualified researchers, ability to withdraw, and more.

  • Box 2-4: Key Points of the Code of Federal Regulations (45 C.F.R. 46) – risk minimization, equitable selection, informed consent, privacy, monitoring, etc.

  • Box 2-5: Exempt Research Examples – various low-risk scenarios that may be exempt from consent but still require IRB review.

  • Table 2-1: Example of Building Knowledge in Nursing Science: Pain and CTR – describes descriptive, explanatory, predictive, and causal aims across multiple studies (Gift 1991; Puntillo 1994; Carson 1994; Puntillo & Ley 2004; Friesner et al. 2006; Demir & Khorshid 2010; Aktas & Karabulut 2019; Özcan & Karagözoğlu 2020; etc.). Findings include descriptions of CTR pain, comparisons with suctioning, analgesia regimens, nonpharmacological interventions, and some instances of no significant differences; one study noted a significant reduction with a breathing relaxation technique combined with analgesia.

  • Table 2-2: Quantitative vs Qualitative Approaches – comparative attributes (philosophical perspective, reasoning style, role of researcher, strategies, data types, sample sizes, designs).

  • Table 2-3: Comparison of Research and EBP – research generates new knowledge and aims to fill gaps; EBP applies knowledge to patient care and measures outcomes; key distinctions in questions, data, and evaluation focus.

  • Table 2-4: IRB components and concerns – risk-benefit analysis, informed consent, privacy, monitoring, safeguards, etc.

  • Table 2-5 (exemptions): Example research exemptions (education, benign behavioral interventions with data anonymity, existing data, public health program evaluations, etc.).


Quick Reference: Key Quotes and Definitions (LaTeX-ready)

  • Belmont principles: {\text{Respect for Persons},\; \text{Beneficence},\; \text{Justice}}

  • Minimal risk: \text{The probability and magnitude of harm are not greater than those encountered in daily life}.

  • Nuremberg Code (summary): voluntary consent is essential; studies must yield fruitful results; avoid unnecessary harm; research must be scientifically valid; investigators must be qualified; participants must be able to withdraw; etc. See Box 2-3 for the full sequence.

  • Declaration of Helsinki (1964, last amended 2013): emphasizes informed consent and participant welfare in biomedical research.

  • IRB composition requirements (minimum): at least five members with diverse expertise and no conflicts of interest; at least one scientist, at least one non-scientist, and at least one member unaffiliated with the organization.

Notes: The above notes synthesize the content from the provided transcript, covering definitions, process steps, aims of research, study designs, historical evolution of nursing as a science, ethics, and future directions. Where specific study details were garbled in the transcript (e.g., parts of Table 2-1), the notes retain the intended interpretation and provide a faithful, organized summary suitable for exam preparation.