Also see attached template file*** The research subject is “All falls reduced in elderly patients in an acute care setting reduced or eliminated with pressure alarms vs. direct camera monitoring.<\/p>\n
Overview\/Description:
\nThe final project for NSG6101 consists of the development of a novel research proposal specific to your role specialization. The project must include an intervention appropriate to nursing practice and consistent with your MSN role option. An alternative to the above includes the selection of a specialty organization to focus research proposals based on the priorities of that organization. Examples of these organizations could include (but are not limited to): Sigma Theta Tau International, American Nurses’ Foundation, Oncology Nursing Society, Association of Nurses in AIDS Care, American Psychiatric Nursing Association, American Association of Critical Care Nurses, National Association of Pediatric Nurse Associates and Practitioners, National League For Nursing, etc.<\/p>\n
Throughout this course you have been developing various sections of the research proposal. This week you will assemble the final proposal (addressing faculty feedback). This paper is to be developed in APA format\/style using the required template and not to exceed 15 pages (excluding title page\/references\/appendices).<\/p>\n
Criteria:
\nIntroduction<\/p>\n
Background and Significance of Problem
\nStatement of the Problem and Purpose of the Study
\nLiterature Review<\/p>\n
Summary of the Evidence for the Proposed Study
\nResearch Question, Hypothesis, and Variables with Operational Definitions<\/p>\n
Theoretical Framework<\/p>\n
Overview and Guiding Propositions(s) Described in Theory
\nApplication of Theory to Your Study\u00e2\u20ac\u2122s\/Project\u00e2\u20ac\u2122s Focus
\nMethodology<\/p>\n
Sample\/Setting: Number and criteria for inclusion and description of place in which data will be collected.
\nSampling Strategy
\nResearch Design: Type (e.g., Quasi-Experimental), description, and rationale for selection.
\nExtraneous Variables (and plan for how controlled).
\nInstruments: Description, validity, and reliability estimates, which have been performed (on a pre-established measure). Include plans for testing validity and reliability of generating your own instrument(s).
\nDescription of the Intervention
\nData Collection Procedures
\nData Analysis Plans
\nDescribe plan for data analysis for demographic variables (descriptive statistical tests).
\nDescribe plan for data analysis of study variables (descriptive and inferential statistical tests).
\nEthical Issues<\/p>\n
Describe ethical considerations and your plan to protect human rights.
\nLimitation of Proposed Study
\nImplications for Practice
\nReferences
\nAppendices<\/p>\n
Informed Consent Letter
\nProcedure section is clear, described in detail, specific, and all inclusive. Written in lay language (as documented by reading level score). Includes risks and benefits relevant to study. Address assent (if applicable).
\nSubmit your assignment to the W10: Assignment 2 Dropbox by Friday, April 29, 2016.<\/p>\n
CRITERIA
\nWEIGHT
\nIntroduction<\/p>\n
Background and Significance of Problem
\n10
\nStatement of the Problem and Purpose of the Study
\n10
\nLiterature Review
\n40
\nResearch Question, Hypothesis, and Variables with Operational Definitions<\/p>\n
Research Question, Hypothesis
\n10
\nVariables with Operational Definitions
\n5
\nTheoretical Framework<\/p>\n
Overview and Guiding Propositions(s) Described in Theory
\n15
\nApplication of Theory to Your Study\u00e2\u20ac\u2122s\/Project\u00e2\u20ac\u2122s Focus
\n15
\nMethodology
\nSample\/Setting: Number and criteria for inclusion and description of place in which data will be collected.
\n15
\nSampling Strategy
\n15
\nResearch Design: Type (e.g., Quasi-Experimental), description, and rationale for selection.
\n10
\nExtraneous Variables (and plan for how controlled).
\n5
\nInstruments: Description, validity, and reliability estimates, which have been performed (on a pre-established measure). Include plans for testing validity and reliability of generating your own instrument(s).
\n20
\nDescription of the Intervention
\n20
\nData Collection Procedures
\n20
\nData Analysis Plans<\/p>\n
Describe plan for data analysis for demographic variables (descriptive statistical tests).
\nDescribe plan for data analysis of study variables (descriptive and inferential statistical tests).
\n20
\nEthical Issues<\/p>\n
Describe ethical considerations and your plan to protect human rights.
\n10
\nLimitations and Implications
\n10
\nScholarly Research
\nReferences and Appendices<\/p>\n
10
\nInformed Consent Letter Procedure section is clear, described in detail, specific, and all inclusive. Written in lay language (as documented by reading level score). Includes risks and benefits relevant to study. Address assent (if applicable).
\n10
\nAcademic Writing<\/p>\n
Free of grammatical, spelling, or punctuation errors. Citations and references written in the correct APA Style.<\/p>\n
30
\nTOTAL
\n300<\/p>\n","protected":false},"excerpt":{"rendered":"
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