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Assignment: Thesis – Chapter 3
Assignment: Thesis – Chapter 3
Write a 700- to 1,050-word rough draft of the third chapter of your master’s thesis, the methods chapter.
HEADLINE WOULD BE: CHAPTER THREE: METHODS
ALSO THE ASSIGNMENT IS JUST A CONTINUATION OF THE PREVIOUS WORKS. TRY AND USE THE SAME REFERNCES IN THE PREVIOUS ASSIGNMENTS. NO NEED TO FORMAT I WILL COMPLETE THIS. JUST WRITE THE PAPER. AS ALWAYS NO SIMILARITY. THE PAPER IS DUE MONDAY BEFORE 6PM.
ALSO, USE THIS AS A REFERENCE WHEN COMPLETELING. PLEASE INCLUDE INTRO, SETTIING, PARTICIPANTS (10 MALE AGES 7 THROUGH 17), INTERVENTION, MATERIALS, MEASUREMENT INSTRUMENTS, PROCEDURE, AND DATA ANALYSIS. I WILL ATTACH THE PREVIOUS ASSIGNMENTS TO GIVE YOU AN IDEA OF WHAT WAS WRITTEN BEFORE.
Chapter Three Sections
Once you have received approval from your chairperson and have organized all of your research materials, you can start to write Chapter Three. Chapter Three starts on a new page in the thesis. Chapter Three is divided into eight main sections: (a) Introduction , (b) Setting , (c) Participants , (d) Intervention , (e) Materials , (f) Measurement Instruments, (g) Procedure , and (h) Data Analysis (see Figure 7.1 for major sections in
Figure 7.1. Major sections in Chapter Three, Methods.
| Name of Researcher(s) | City, State, and Country / School or College and University | Affiliation
(student, faculty, or staff and id)
|
Type of Research
(research study, *funded research, or other) |
| Diane Aybar | Miami, Florida
University of Phoenix |
IRN: LEAVE THIS BLANK | Research Study
|
| * If research is funded, please complete the following agency information. Otherwise, leave blank. | |||
| agency submitted to | submission date | location of project | |
| ?????University of Phoenix
|
9/8/2016 | ?????Miami, FL | |
| 1. Title of the Research Study/Dissertation:
Sexually Abused Male Serial Killers 2. Classification of the Study: a) Will primary data collection from human subjects be done in this study? ( FORMCHECKBOX ) Yes, original data only is collected from human subjects and no archival data will be used. ( FORMCHECKBOX ) Yes, both original data from human subjects and archival data will be collected and used. ( FORMCHECKBOX ) No, only archival data will be used. b) Are the research study results generalizable or relevant to a larger population or only relevant to one organization or entity? ( FORMCHECKBOX ) Results are generalizable to a larger population. ( FORMCHECKBOX ) Results are relevant only to one organization or entity.
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| 3. Purpose and Anticipated Study Goal(s) and Benefits: Briefly describe the following:
The purpose of the study: The purpose of this study is to understand the whether there is a prevention in serial killer at a young age in males. The anticipated study goal(s): The anticipated study goal to is find solutions to prevent future serial killings. The benefits of the study to the subjects, to the organization, and to society: The benefits of this study is to help organizations understand and come up with possible solutions to prevent serial killings to protect society in the future from being the victim of this crime. Assignment: Thesis – Chapter 3 |
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| 3.1 Data Usage and Ownership: If your research involves access to, and/or use of, a pre-existing private or restricted database (one that is not open access/publically available), please briefly describe the type of data in the database, the organization or individual owner or controller of the data, how the data will be accessed and how data confidentiality will be ensured.
a) Does this research study involve access to, or use of public, open access databases or datasets, resources, recruitment lists, contact information for potential subjects or any other pre- existing public data? (Note that “open access” means free and available to the general public without restriction or prior permission needed.) ( FORMCHECKBOX ) No ( FORMCHECKBOX ) Yes (Please describe here) b) Does this research study involve access to, or use of private databases or datasets, private resources or recruitment lists, contact information for potential subjects or any other pre-existing private data? ( FORMCHECKBOX ) No ( FORMCHECKBOX ) Yes (Please describe here and document permission granted for access and use) c) During data collection or subject recruitment, will access be needed to any health information created, received or archived by health care providers, clearinghouses, or health care plans that pertains to the past, present or future health conditions or provision of health care to an individual living or deceased? ( FORMCHECKBOX ) Yes ( FORMCHECKBOX ) No ( FORMCHECKBOX ) HIPAA compliance (if health records are used, please discuss here and address HIPAA compliance) d) Will school or student related data be collected in this study? ( FORMCHECKBOX ) Yes, individual student data ( FORMCHECKBOX ) Yes, aggregate student data ( FORMCHECKBOX ) No ( FORMCHECKBOX ) FERPA compliance (if student data is used, please explain here and address FERPA compliance)
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| 4. Project Description: Briefly explain and address the following questions as indicated:
a) Who are the subjects of this study and where are they located? (for example, lawyers in private practice in the State of Ohio) b) What are the subjects expected to do as participants in this study and what is the time commitment involved? Please explain. If class time is used, please describe the activities planned for non-participants. c) Will a pilot study be conducted before the primary data collection occurs? ( FORMCHECKBOX ) No ( FORMCHECKBOX ) Yes d) What is the research method and design? Check all that apply: ( FORMCHECKBOX ) quantitative analysis ( FORMCHECKBOX ) qualitative analysis ( FORMCHECKBOX ) mixed methods ( FORMCHECKBOX ) phenomenological ( FORMCHECKBOX ) case study ( FORMCHECKBOX ) experimental ( FORMCHECKBOX ) quasi experimental ( FORMCHECKBOX ) Delphi ( FORMCHECKBOX ) other (specify) ___________________________________________ e) How will data be collected? Check any that apply: ( FORMCHECKBOX ) face to face interview ( FORMCHECKBOX ) focus group ( FORMCHECKBOX ) online survey ( FORMCHECKBOX ) mail survey ( FORMCHECKBOX ) telephone survey ( FORMCHECKBOX ) onsite survey ( FORMCHECKBOX ) email survey ( FORMCHECKBOX ) Skype or related technology ( FORMCHECKBOX ) other (specify) ____________________________ f) Where will data collection occur? Check any that apply and specify the location(s) below. ( FORMCHECKBOX ) organizational site ( FORMCHECKBOX ) online ( FORMCHECKBOX ) private premises ( FORMCHECKBOX ) public facility ( FORMCHECKBOX ) open access site ( FORMCHECKBOX ) other ( FORMCHECKBOX ) not applicable Location __________________________________________ g) What is the degree or magnitude of risk/stress (physical, psychological, emotional, legal, financial) to the human subjects because of their participation in this study? ( FORMCHECKBOX ) minimal risk/stress, not greater than encountered in ordinary daily life/activities or routine tests. ( FORMCHECKBOX ) greater than minimal risk/stress with potential for direct benefit to the individual subjects ( FORMCHECKBOX ) greater than minimal risk/stress with little/no potential direct benefit to individual subjects h) If greater than minimal risk/stress to the human subject is possible, please explain how the risk/stress will be mitigated or lessened. i) Are any third parties assisting with this study that will have access to the data? ( FORMCHECKBOX ) No ( FORMCHECKBOX ) Yes (specify) ______________________________________ j) Will any aspect of the study take place outside of the United States? ( FORMCHECKBOX ) No ( FORMCHECKBOX ) Yes (specify where) _______________________________________ Note that IRB approval may be needed in the country where research is |
