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In other words, specify anonymity of demographic data detached from collected information, how will investigator ensure confidentiality of data, etc.The signed informed consent form(s) must be stored separately from the participant’s data.They are not intended to serve as boilerplate selections for proposals.
Be sure to include an informed consent form and debriefing statement.
Specify any anticipated risks or benefits (even if in informed consent, restate here separately for IRB purposes) – if none, specify none.
Implications: Please state what your expected outcomes and their implications are with respect to prior research, theory and rationale.
References: Provide a reference section for the studies, theories cited in introduction, brief literature review.
The following links provide examples of the informed consent, debriefing, answers to questions on the “Request for Exempt Status” form and abstracts.
The samples are designed to provide examples from actual proposals and serve as a guide for completing proposals.Kindly provide your name, title of investigation, project number and date of IRB approval.Preferred sequence of documentation: Please allow a minimum of 2-3 weeks from date of IRB meeting for processing time for Full Review or a minimum of 1-2 weeks from date of IRB meeting for processing time for Expedited Review, and submit to your school IRB representative.Please provide the following on a separate sheet(s) of paper: Principal Investigator: (Your name) Research Supervisor: (Faculty, Staff, or Administrator) Project Title: Course: (Only if relevant) Date of Application: Funding source/Representative of study: (if applicable) (e.g., Roche Pharmaceuticals, 00, dispensed through Development Office, NDNU) Statement of purpose: (One paragraph) What is the rationale for the proposed study you plan to conduct?Specify your question of interest and research objective.Note: Please check with site/organization/institution where you plan to gather participants as many places have their own IRB requirements and/or will require permission before data collection can begin.Specify if through random means, where, how, not any friends, family, etc.Design: Type of research design, variables of interest, how measured, data collection, analysis.State how data will be collected, analyzed, coded, stored (ethically, i.e., in locked file) – and expected analyses and outcomes.Brief introduction/literature review In a couple of sentences, state your hypothesis(es) /expected outcomes, relaying the general question stated.Method Section: Participants: (who, how many, how and where recruited, appropriate permission letters need to be attached for sites, agencies, organizations, schools).