Design |
- Select the research design
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Identify the population, select the sample, sampling method, & determine sample size |
Identify methods to measure variables & data collection methods |
Obtain permission to use instruments or develop instruments, data collection forms, and consent forms/letters |
Obtain physician permission to recruit patients &.or institutional and university IRB approvals |
Conduct a pilot study and revise
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Chapter II - Review of literature & theoretical framework |
- Review of the literature & theoretical framework- 7 to 12 pages in proposal; 10 to 25 or more in theses or dissertation
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- Present an integrated review of research studies; do not write a paragraph summarizing each study
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- Integrate content so you write separate paragraphson populations & samples; sampling methods; designs; instruments; data collection methods; data analysis; and findings. Integrate content so you write separate paragraphson populations & samples; sampling methods; designs; instruments; data collection methods; data analysis; and findings.
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- Critique the quality of the research that has been done Critique the quality of the research that has been done
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- Identify flaws, shortcomings, or gaps in the literature
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- E.G., the problem has not been investigated in children, or adults with cancer; need to use a random sample
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- Identify research that needs to be done in the future to fill the gaps, or correct the flaws in prior studies
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- Identify how the proposed study will fill one of the gaps in the research
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- Briefly describe the theoretical/conceptual framework for the study
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- State what proposition or particular concepts from the framework you are examining in your study
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- Tie the proposed study to the framework
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- Complete this section of the proposal by restating the research questions or hypotheses
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Chapter III - Methods |
- Methods chapter explain how study will be implemented to answer the research questions or test the hypotheses; usually 15 to 20 pages in proposal; additional pages for appendices that include copies of each data collection instrument; letters to tool authors, physicians, etc.; consent forms or consent letters.
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- Design - experimental, quasi-experimental, descriptive, etc.
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- Accessibility & recruitment of subjects
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- Operational definition of each variable
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- Reliability & validity of instruments
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- Instrument development & scoring
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- Author's permission to use instrument
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- Physician permission to recruit patients
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- Institution & university IRB or HSC approvals
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- Consent forms or consent letters
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- Detailed description of intervention in experimental or quasi-experimental study
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- Who, what, where, when & how data will be collected
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