BUSI 885 Recruitment and Selection Strategies Dissertation


BUSI 885 Recruitment and Selection Strategies Dissertation

BUSI 885 Recruitment and Selection Strategies Dissertation

So we are in the final stretch of the second half. I will use this to post other stuff that needs to be completed. For now here are the tasks at hand

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  • Task 9 – IRB Package
  • Task 10 – Section 2: Reliability and Validity
  • Task 11 – First Draft of Section 2
  • Task 12 – Final Draft of Section 2
  • Task 13 – First Draft of Section 1 & 2
  • Task 14 – Second Draft of Section 1 & 2 and Proposal Defense Presentation
  • Task 15 – Proposal Defense
  • Task 16 – Final Draft of Section 1 & 2
  • Task 17 – Field Study Plan

APPLICATION INSTRUCTIONS 1. Complete each section of this document by using your tab key to move your cursor to each gray form field and providing the requested information. 2. If you have questions, hover over the blue (?), or refer to the IRB Application Instructions for additional clarification. 3. Review the IRB Application Checklist. 4. Email the completed application, with the following supporting documents (as separate word documents) to irb@liberty.edu: a. Consent Forms, Permission Letters, Recruitment Materials b. Surveys, Questionnaires, Interview Questions, Focus Group Questions 5. If you plan to use a specific Liberty University department or population for your study, you will need to obtain permission from the appropriate department chair/dean/coach/etc. Submit documentation of permission (email or letter) to the IRB along with this application and check the indicated box below verifying that you have done so. 6. Submit one signed copy of the signature page (available on the IRB website or electronically by request) to any of the following: a. Email: As a scanned document to irb@liberty.edu b. Fax: 434-522-0506 c. Mail: IRB 1971 University Blvd. Lynchburg, VA 24515 d. In Person: Green Hall, Suite 2845 7. Once received, the IRB processes applications on a first-come, first-served basis. 8. Preliminary review may take up to 3 weeks. 9. Most applications will require 3 sets of revisions. 10. The entire process may take between 1 and 2 months. 11. We cannot accept applications in formats other than Microsoft Word. Please do not send us One Drive files, Pdfs, Google Docs, or Html applications. Exception: The IRB’s signature page, proprietary instruments (i.e., survey creator has copyright), and documentation of permission may be submitted as pdfs.BUSI 885 Recruitment and Selection Strategies Dissertation

Note: Applications and supporting documents with the following problems will be returned immediately for revisions: 1. 2. 3. 4. Grammar, spelling, or punctuation errors Lack of professionalism Lack of consistency or clarity Incomplete applications **Failure to minimize these errors will cause delays in your processing time** ______________________________________________________________________________ Rev 4/2019 1 II. BASIC PROTOCOL INFORMATION 1. STUDY/THESIS/DISSERTATION TITLE (?) Title: 2. PRINCIPAL INVESTIGATOR & PROTOCOL INFORMATION (?) Principal Investigator (person conducting the research): Professional Title (Student, Professor, etc.): Student School/Department (School of Education, LUCOM, etc.): School of Business Phone: LU Email: Check all that apply: Faculty Online Graduate Student Staff Residential Undergraduate Student Residential Graduate Student Online Undergraduate Student This research is for: Class Project Master’s Thesis Scholarly Project (DNP Program) Doctoral Dissertation Faculty Research Other: If applicable, indicate whether you have defended and passed your dissertation proposal: N/A No (Provide your defense date): Yes (Proceed to Associated Personnel Information) 3. ASSOCIATED PERSONNEL INFORMATION (?) Co-Researcher(s): School/Department: Phone: LU/Other Email: Faculty Chair/Mentor(s): School/Department: School of Business Phone: 4 LU/Other Email: Non-Key Personnel (Reader, Assistant, etc.): School/Department: School of Business Phone: LU/Other Email: Consultant/Methodologist (required for School of Education EdD/PhD candidates): School/Department: Phone: LU/Other Email: 4. USE OF LIBERTY UNIVERSITY PARTICIPANTS (?) Do you intend to use LU students, staff, or faculty as participants OR LU student, staff, or faculty data in your study? No (Proceed to Funding Source) Yes (Complete the section below) # of Participants/Data Sets: Department/Source: Class(es)/Year(s): Department Chair: Rev 4/2019 2 Obtaining permission to utilize LU participants (check the appropriate box below): SINGLE DEPARTMENT/GROUP: If you are including faculty, students, or staff from a single department or group, you must obtain permission from the appropriate Dean, Department Chair, or Coach and submit a signed letter or date/time stamped email to the IRB indicating approval to use students from that department or group. You may submit your application without having obtained this permission; however, the IRB will not approve your study until you provide proof of permission. I have obtained permission from the appropriate Dean/Department Chair/Coach and attached the necessary documentation to this application. I have sought permission and will submit documentation to the IRB once I receive it from the appropriate Dean/Department Chair/Coach. MULTIPLE DEPARTMENTS/GROUPS: If you are including faculty, students, or staff from multiple departments or groups (i.e., all sophomores or LU Online), the IRB will need to seek administrative approval on your behalf. I am requesting that the IRB seek administrative approval on my behalf. 5. FUNDING SOURCE (?) BUSI 885 Recruitment and Selection Strategies Dissertation

Is your research funded? No (Proceed to Study Dates) Yes (Complete the section below) Grant Name/Funding Source/Number: Funding Period (Month & Year): 6. STUDY DATES (?) When do you plan to perform your study? (Approximate dates for collection/analysis): Start (Month/Year): January 2020 Finish (Month/Year): May 2020 7. COMPLETION OF REQUIRED CITI RESEARCH ETHICS TRAINING (?) List Course Name(s) (Social and Behavioral Researchers, etc.): Social and Behavioral Researchers & CITI Conflicts of Interest Date(s) of Completion: 01/20/2019 III. OTHER STUDY MATERIALS AND CONSIDERATIONS 8. STUDY MATERIALS LIST (?) Please indicate whether your proposed study will include any of the following: Recording/photography of participants (voice, video, or images)? Yes Participant compensation (gift cards, meals, extra credit, etc.)? Yes Advertising for participants (flyers, TV/Radio advertisements)? Yes More than minimal psychological stress? Yes Confidential data collection (participant identities known but not revealed)? Yes Anonymous data collection (participant identities not known)? Yes Archival data collection (data previously collected for another purpose)? Yes Extra costs to the participants (tests, hospitalization, etc.)? Yes The inclusion of pregnant women (for medical studies)? Yes More than minimal risk?* Yes Rev 4/2019 No No No No No No No No No No 3 Alcohol consumption? Protected Health Information (from health practitioners/institutions)? VO2 Max Exercise? Pilot study procedures (which will be published/included in data analysis)? Use of blood? Total amount of blood: Blood draws over time period (days): The use of rDNA or biohazardous material? The use of human tissue or cell lines? Fluids that could mask the presence of blood (including urine/feces)? Use of radiation or radioisotopes? Yes Yes Yes Yes Yes No No No No No Yes Yes Yes Yes No No No No *Note: Minimal risk is defined as “the probability and magnitude of harm or discomfort anticipated in the research are not greater in and of themselves than those ordinarily encountered in everyday life or during the performance of routine physical or physiological examinations or tests. [45 CFR 46.102(i)]. If you are unsure if your study qualifies as minimal risk, contact the IRB. 9. INVESTIGATIONAL METHODS (?) Please indicate whether your proposed study will include any of the following: The use of an investigational new drug (IND) or an approved drug for an unapproved Use? No Yes (Provide the drug name, IND number, and company): The use of an investigational medical device or an approved medical device for an unapproved Use? No Yes (Provide the device name, IDE number, and company): IV. PURPOSE 10. PURPOSE OF RESEARCH (?)BUSI 885 Recruitment and Selection Strategies Dissertation

Write an original, brief, non-technical description of the purpose of your research. Include in your description your research hypothesis/question, a narrative that explains the major constructs of your study, and how the data will advance your research hypothesis or question. This section should be easy to read for someone not familiar with your academic discipline: The purpose of this study is to explore the use or nonuse of atmospherics within small coffee shops in the Midwest and the impact that the use or nonuse of atmospherics has on customer loyalty of coffee shops. The research questions will address current customers of coffee shops and current owners, managers, and employees of coffee shops. Questions for owners, employees, and managers of coffee shops will address specific atmospheric techniques utilized. Questions for current customers of coffee shops will address the feelings regarding atmospherics and customer loyalty. Participants will be observed and interviewed. V. PARTICIPANT INCLUSION/EXCLUSION CRITERIA 11. STUDY POPULATION (?) Provide the inclusion criteria for the participant population (e.g., gender, age range, ethnic background, health status, occupation, employer, etc.): Participants include stakeholders of coffee shops within the Midwest. Stakeholders consist of customers, owners, employees, and managers of coffee shops. Rev 4/2019 4 Provide a rationale for selecting the above population (i.e., Why will this specific population enable you to answer your research question?): This specific population will help the researcher understand information about coffee shops, atmospherics, and customer loyalty. This population will be stakeholders of coffee shops, therefore, will be able to provide information for the study. Will your participant population be divided into different groups (i.e., experimental and control groups)? No Yes (Describe the groups and explain how groups will be selected/assigned.): One participant group will consist of customers of coffee shops. Another participant group will consist of employees, managers, and owners of coffee shops. Are you related to any of your participants? No Yes (Explain): Indicate who will be excluded from your study population (e.g., persons under 18 years of age): Persons under the age of 18 If applicable, provide rationale for involving any special populations (e.g., children, ethnic groups, individuals with impaired decision-making ability or low socio-economic status, or prisoners): N/A Provide the maximum number of participants you plan to enroll for each participant population and justify the sample size (You will not be approved to enroll a number greater than the number listed. If at a later time it becomes apparent that you need to increase your sample size, submit a Change in Protocol Form and wait for approval to proceed.): 30. The sample should generate enough information that data saturation occurs. This sample size should provide enough data to understand coffee shops, atmospherics, and customer loyalty. ANSWER THE FOLLOWING QUESTION ONLY IF YOU ARE CONDUCTING A PROTOCOL WITH NIH, FEDERAL, OR STATE FUNDING: Researchers sometimes believe their particular project is not appropriate for certain types of participants. These may include, for example, women, minorities, and children. If you believe your project should not include one or more of these groups, please provide your justification for their exclusion. Your justification will be reviewed according to the applicable NIH, federal, or state guidelines: 12. TYPES OF PARTICIPANTS (?) Who will be the focus of your study? (Check all that apply) Normal Participants (Age 18-65) Pregnant Women Minors (Under Age 18) Fetuses Over Age 65 Cognitively Disabled College/University Students Physically Disabled Active-Duty Military Personnel Participants Incapable of Giving Consent Rev 4/2019 5 BUSI 885 Recruitment and Selection Strategies Dissertation

Discharged/Retired Military Personnel Inpatients Outpatients Patient Controls Prisoners or Institutional Individuals Specific Ethnic/Racial Group(s) Other potentially elevated risk populations Participant(s) related to the researcher Note: Only check the boxes if the participants will be the focus (for example, ONLY military or ONLY students). If they just happen to be a part of the broad group you are studying, you only need to check “Normal Participants.” Some studies may require that you check multiple boxes (e.g., Korean males, aged 65+). VI. RECRUITMENT OF PARTICIPANTS 13. CONTACTING PARTICIPANTS (?) Describe in detail how you will contact participants regarding this study (include the method(s) used—email, phone call, social media, snowball sampling, etc.): The researcher will ask participants in person using a script located on a recruitment letter. The script will be included as a separate document in this application. 14. SUBMISSION OF RECRUITMENT MATERIALS (?) Submit a copy of all recruitment letters, scripts, emails, flyers, advertisements, or social media posts you plan to use to recruit participants for your study as separate Word documents with your application. Recruitment templates are available on the IRB website. Check the appropriate box: All of the necessary recruitment materials will be submitted with my application. My study strictly uses archival data, so recruitment materials are not applicable. If you plan to provide documents in a language other than English: I will submit a translated copy of my recruitment materials along with the English version(s). 15. LOCATION OF RECRUITMENT (?) Describe the location, setting, and timing of recruitment: Recruitment of participants will take place at several coffee shops in the Midwest. The researcher will first obtain permission to use participants from each location from the owner or management of the coffee shops. After permission is granted, the researcher will conduct the study. 16. SCREENING PROCEDURES (?) Describe any procedures you will use to ensure that your participants meet your study criteria (e.g., a screening survey or verbal confirmation to verify that participants are 18 or older): Verbal confirmation that the participants are over the age of 18 will be required prior to participating in the study. 17. CONFLICTS OF INTEREST (?) Conflicts of interest are “situations in which financial or other personal considerations may compromise, or have the appearance of compromising, an investigator’s judgement in conducting or reporting research” AAMC, 1990. Rev 4/2019 6 Do you have a position of academic or professional authority over the participants (e.g., You are the participants’ teacher, principal, supervisor, or district/school administrator.)? No Yes (Explain what safeguards are in place to reduce the likelihood of compromising the integrity of the research, e.g., addressing the conflicts in the consent process and/or emphasizing the pre-existing relationship will not be impacted by participation in the research.): Do you have any financial or personal conflicts of interest to disclose (e.g., Do you or an immediate family member receive income or other payments, own investments in, or have a relationship with a non-profit organization that could benefit from this research?)? BUSI 885 Recruitment and Selection Strategies Dissertation

No (Proceed to Procedures) Yes (State the funding source/financial conflict and then explain what safeguards are in place to reduce the likelihood of compromising the integrity of the research.): VII. RESEARCH PROCEDURES 18. PROCEDURES (?) Write an original, non-technical, step-by-step description of what your participants will be asked to do during your study and data collection process. If you have multiple participant groups, (e.g., parents, teachers, and students) or control and experimental groups, please specify which group you are asking to complete which task(s). You do not need to list signing/reading consent as a step. Time to Participant Group(s) Complete (All, Group A, Group B, Step/Task/Procedure Procedure Control Group, (Approx.) Experimental Group, etc.) 1. Take part in a recorded interview 30 minutes Customers 2. Take part in a recorded interview Owners, employees, and 30 minutes managers 3. Observations of coffee shops will take Participants will have no 60 minutes place. formal obligations. 4. 5. 6. 7. 8. Note: For complex study designs, additional diagrams, timelines, or figures may be submitted separately. 19. SUBMISSION OF DATA COLLECTION INSTRUMENTS/MATERIALS (?) Submit a copy of all instruments, surveys, interviews questions, outlines, observation checklists, prompts, etc. that you plan to use to collect data for your study as separate Word documents with your application. Pdfs are ONLY acceptable for proprietary instruments. Check the appropriate box: All of the necessary data collection instruments will be submitted with my application. My study strictly uses archival data, so data collection instruments are not applicable. Rev 4/2019 7 If you plan to provide documents in a language other than English: I will submit a translated copy of my study instrument(s) along with the English version(s). 20. STUDY LOCATION (?) Please state the actual location(s)/site(s) in which the study will be conducted. Be specific (include city, state, school/district, clinic, etc.): Penny’s Perks, Dowell, Illinois; Crown Brew, Carterville, Illinois; The Rail Coffeehouse, Centralia, Illinois; Foundry, Lebanon, Illinois; The CoffeeHouse Company, O’Fallon, Illinois Note: Investigators must submit documentation of permission from some research sites to the IRB prior to receiving approval. If your study involves K-12 public schools, district-level approval is acceptable as opposed to submitting separate permission documentation from each school. If your study involves colleges or universities, hospitals, or prisons, you may also need to seek IRB approval from those institutions. You may seek permission prior to submitting your IRB application; however, do not begin recruiting participants. If you find that you need a conditional approval letter from the IRB to obtain permission, the IRB will provide one once you have completed all requested revisions. VIII. DATA ANALYSIS 21. NUMBER OF PARTICIPANTS/DATA SETS (?) Estimate the number of participants to be enrolled or data sets to be collected: 30 22. ANALYSIS METHODS (?) Describe how the data will be analyzed: The researcher will analyze the data. Each piece of data will be kept, and analyzed. The researcher will analyze the data by looking for themes that emerge from the data collected. Each piece of data will be compared to data collected throughout the study. Please describe what will be done with the data and the resulting analysis (Include any plans for publication or presentation.): After the data is analyzed, the researcher will include it in the dissertation. IX. PARENTAL/GUARDIAN CONSENT 23. PARENTAL/GUARDIAN CONSENT REQUIREMENTS (?) Does your study require parental/guardian consent? (If your participants are under 18, parental/guardian consent is required in most cases.) BUSI 885 Recruitment and Selection Strategies Dissertation

No (Proceed to Child Assent) Yes (Answer the following question) Does your study entail greater than minimal risk without the potential for benefits to the participant? No Yes (Consent of both parents is required) X. ASSENT FROM CHILDREN 24. CHILD ASSENT (?) Is assent required for your study? (Assent is required unless the child is not capable of assenting due to age, psychological state, or sedation OR the research holds out the prospect of a direct benefit that is only available within the context of the research.) No (Proceed to Consent Procedures) Yes Rev 4/2019 8 Note: If the parental consent process (full or part) is waived (See XIII below) assent may be also. See the IRB’s informed consent page for more information. XI. PROCESS OF OBTAINING INFORMED CONSENT 25. CONSENT PROCEDURES (?) Describe in detail how and when you will provide consent/assent/parental consent information (e.g., as an attachment to your recruitment email, as the first page participants see after clicking on the survey link, etc.): Consent will be included on a consent form before participation in the interview process occurs

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