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ENGLISH 2960
Project #2
Ethics in the Workplace: A Critical Analysis of the film
Glengarry GlenRoss
*Analysis: is a process of breaking down something complex
into simpler elements that will make it more understandable.
*Critical Analysis: an analysis with an argumentative and
evaluative edge (the writer is attempting to persuade the reader
of something).
For Project #2 you will apply the notion of “ethics in the
workplace” to the film Glengarry GlenRoss. Further, you will
write a Critical Analysis of one aspect of the movie. The
direction in which you take this analysis (the aspect of the film
which you analyze) is entirely up to you. I do suggest that you
focus on one particular scenario (your choice) from the film that
depicts an instance of unethical behavior in the workplace.
Keep in mind your reading of Chapter 1, and on the below
definitions of Kant's Categorical Imperative, Utilitarianism, and
Ethical Relativism. I would like for you to somehow apply one
of these below principles to your analysis. Length: 3 pages,
typed, double-spaced.
1. Kant's Categorical Imperative:
The most fundamental of all the liberal principles handed down
to us from the Enlightenment and the very cornerstone of our
civilization is the "categorical imperative" of Immanuel Kant:
namely, that one cannot act on that maxim which one cannot
will to be universal. In other words, if it's OK for me to do it, it
has to be OK for everybody to do it. If it's not OK for
everybody to do it, then it's not OK for me to do it either. This
principle is so deeply ingrained in us, along with the contempt
we feel for what we call "hypocrisy" when people violate it, that
we take it for granted.
2. Utilitarianism:
A doctrine that “the useful is the good,” and that the
determining consideration of right conduct should be the
usefulness of its consequences. Specifically – a theory that the
aim of action should be the largest possible balance of pleasure
over pain or the greatest happiness of the greatest number.
3.Ethical Relativism:
In ethics,the belief that nothing is objectively right or wrong
and that the definition of right or wrong depends on the
prevailing view of a particular individual, culture, or historical
period.
_____________________________________________________
_
As you work, keep these strategies in mind:
1.) Zero in on key elements (relevant to your overall topic).
2.) View the film through a critical lens. (How are you watching
and understanding this film? Through ‘political’ eyes? Through
‘social’ eyes? Through ‘psychoanalytical’ eyes?)
3.) Compare the film to something similar. (Have you read
about, seen, heard of something that reminds you of the content
of this film? Does something inform how you understand this
film?)
*Remember: For most analyses, you will utilize/use a
combination of the above 3 approaches.
University of Phoenix Material
Proposal Worksheet
Each team member will pick an article for this worksheet.
Replicate these set of questions for each team member for this
worksheet.
Team member name: Kevin Hwang
Citation of article: Hely, J. M., Jamieson, G. A., & Dunstan, D.
(2011). Smoking Cessation: A Combined Cognitive Behavioural
Therapy and Hypnotherapy Self-Help Treatment
Protocol. Australian Journal of Clinical & Experimental
Hypnosis, 39(2), 196–227. Retrieved from https://search-
ebscohost-
com.contentproxy.phoenix.edu/login.aspx?direct=true&db=a9h
&AN=95317811&site=ehost-live&scope=site
1. What is the author’s goal?
The author’s goal with this article was to show the efficacy of
combining two forms of therapy, Cognitive Behavioral Therapy
and Hypnotherapy, to help individuals to reduce cigarette intake
and/or achieve cessation of smoking.
2. What questions remain unanswered?
The question that still remains unanswered is if whether or not
hypnosis alone can help decrease a smoker’s urge to smoke.
3. If I had to design an experiment to test this hypothesis, what
would I do?
If I had to design an experiment to test this hypothesis, I would
have 3 separate groups. The first group would only be subject to
CBT, while the second group would be subject only to
Hypnotherapy. The third group would get the combined efforts
of both types of therapy.
4. What are the independent, dependent, and control variables?
The independent variable would be the type of therapy that is
being administered to the group, CBT and hypnotherarpy. The
dependant variable would be amount of cigarettes smoked
during the experiment. The control variables would be amount
of therapies that the subjects would have to undergo.
Team member name:Julie Brandenburg
Citation of article: Hypnotherapy for smoking cessation
(Review)
2010The Cochrane Collaboration1-41
Barnes J, Dong CY, McRobbie H, Walker
N, Mehta M, Stead LF
1. What is the author’s goal?
The objective of this article is to figure out if hypnosis can be
just as effective or even have a greater effect on quitting
smoking over a six month period. The hypnosis would be
compared to other interventions and verses no treatment.
2. What questions remain unanswered?
Would there be a difference in the results if the individuals
were looked at from a class perspective? Would someone who
was poor have the same success rate as someone who had an
open checkbook?
3. If I had to design an experiment to test this hypothesis, what
would I do?
Not only would I have chosen individuals that wanted to quit
smoking and had smoked for years. I would’ve also collected
the same number of women verse men and the same number of
poor versus the wealthy. My objective would be to see if it’s
easier for men or women to quit with this process. Also, if
someone has the funds to invest in the hypnosis more than once
would the results differ. Compared to a poor individual that
wouldn’t have the funds to follow up with more sessions
4. What are the independent, dependent, and control variables?
The independent variable would be the type of therapy that was
used within the group study which was the hypnosis. The
dependent would be the number of cigarettes that the
individuals smoked during the study period. The control
variable would be the number of therapy sessions that followed
the hypnosis session or if there was more than one hypnosis
session.
Team member name: Patrice Scope
Citation of article: Robinson, T. E., & Berridge, K.
C. (2003). Addiction. Annual Review of Psychology, 54, 25-53
1. What is the author’s goal?
The authors’ goal for this particular article was to examine the
various theories about how drugs affect our psychological
pathways and later turns into addictions. One of the proposed
theories is a type of dysfunction on our frontol cortical systems
which usually control decision making and ultimately lead to
the compulsive behavior of an addiction.
2. What questions remain unanswered?
Does NAcc-related circuitry play a primary role in drug
addictions like drug sensitization?
3. If I had to design an experiment to test this hypothesis, what
would I do?
Hypothesis: The system NAcc-related circuitry does play a
major role in drug addiction while drug sensitization plays a
secondary role. To test this hypothesis, I would run various
tests on drug dependent individuals (preferably, the same drug)
and compare the results of the NAcc-related system to drug
sensitization. The number of Dopamine receptors in the NAcc
will be measured for the results.
4. What are the independent, dependent, and control variables?
The independent variable would be the amount of drug. For
example, the experiment could be set up on a scale with how
many usages the individual partake in on a daily basis. The
dependent variable would be the number of Dopamine receptors
that is found in the NAcc. The control group would be a group
of individuals that do not partake in drugs
Team member name:Zenobia J. Bostic
Citation of article:Riegel, B. Tonnies, S. (2011). Hypnosis for
smoking cessation: The Effectiveness of some basic principles
of hypnotherapy without using formal trace--- A Case Study.
Journal Of Smoking Cessation, 6 (2), 83 – 84.
doi:http://dx.doi.org.contentproxy.phoenix.edu/10.1375/jsc.6.2.
83
1. What is the author’s goal?
The author’s goal to highlight some insight on some
intervention strategies when using the basic principles of
hypnotherapy.
2. What questions remain unanswered?
How deep is the roots of the mental addiction of the
subconscious mind(thoughts)?
3. If I had to design an experiment to test this hypothesis, what
would I do?
I would try to design an experiment to test “How to tap into an
individual subconscious to gain knowledge of how the addiction
started and what strategies from hypotherapy will connect with
the habits or behavior to help them quit without the triggers.
4. What are the independent, dependent, and control variables?
The independent variable was the choosing hypnosis with a high
expectation of success. Dependent variable Mr. D a regular
smoker for about 45 years tried to quit several times in those
years. He had never stayed abstinent for more than one month.
The control variable would be his motivation to quit, he spoke
about the growing loneliness of smokers in today’s society.
Team member name: Jennifer Ross
Citation of article: Timothy P. Carmosy, Carol Duncan, Joel A.
Simons, Sharon Solkowitz, Joy Huggins, Sharon Lee, Kevin
Delucchi; Hypnosis for Smoking Cessation: A Randomized
Trial, Nicotine & Tobacco Research, Volume10, Issue 5, 1 May
2008, Pages 811-818,https://doi-
org.contentproxy.phoenix.edu/10.1080/14622200802023833
1. What is the author’s goal?
The goal of this article was to determine whether hypnosis is
more effective in helping smokers quit then just regular
behavior counseling.
2. What questions remain unanswered?
The question I have is does hypnosis alone help smokers quit.
3. If I had to design an experiment to test this hypothesis, what
would I do?
I would set up different test subjects. Some with just hypnosis,
and the same number getting both behavior couseling and
hypnosis. I would see the status of all groups in 7 to 10 10 days
then again at 3 months, 6 months, 9 month, and one year.
4. What are the independent, dependent, and control variables?
independent variable is behavioral counciling, dependent is
hypnosis only group, control would be hypnosis.
After reviewing each team member’s submission, answer the
following questions as a team:
1. What is your research question?
How can hypnosis help smokers decrease their urge to smoke?
2. What is your hypothesis?
Since studies show that hypnosis can be used to
alter automatic mental processes, individuals who undergo
hypnotherapy will see a decrease in urge to smoke.
1
3
Methods PaperLearning Team APSY/335
February 4th, 2019
Brian Claybrook
Methods Paper
As previously discussed during our proposal assignment in
Week Two, the area of research we chose to focus on revolves
around question and hypothesis of whether or not hypnosis
could help smokers decrease their urge to smoke. In this paper,
we will discuss our sampling methods, the type of statistics,
descriptive or inferential, we will use, definitions of our
variables, and how we will operationalize said variables. The
purpose of this Methods Paper is so that we, as a team, can
show how to properly set up and execute a research study.
Sampling Method
The sampling method that we choose to go with was the
stratified sampling method. A stratified sampling method refers
to a methodology where researchers divide a total population
into smaller groups known as strata. According to The
Economic Times (2019), “strata are formed based on some
common characteristics in the population data.” After the
population is divided into strata, the researchers would then
randomly select the sample from each group. In 2016, it was
determined that 37.8 million Americans smoke in the United
States. Since our team wanted to get a sample that gave us true
and unbiased data without having a humongous group, we
decided to take a look at the nation’s smoking population.
According to the data collected by the CDC from a survey
conducted in 2016, there were more men than women smokers,
by four percent. Thus, we choose to select a hundred adults,
54% men and 46% women. Out of the current number of
smokers, it had been polled that 18% were of the ages 45 to 64,
17% were 25 to 44, and the remain 13% were 18 to 24 years old
(Centers for Disease Control Prevention, 2016). Having this
information, we decided to make strata according to gender as
well as age. From there, we will take samples from each stratum
to create a proportionally random sampling group to test our
hypothesis on.
Descriptive or Inferential Statistics
For this study, our group decided to use inferential statistics.
The reasoning behind this was because inferential statistics
revolves around the concept that the data collected from the
sample will be used to make inferences about the larger
population from which the sample was drawn from (Frost,
2019). In layman’s terms, this means that the data that will be
collected from the research will be used to make a general claim
regarding the subject matter. In the case of our study, depending
on what the study shows, we may say that our findings show us
that the hypnosis may or may not possibly reduce the urge to
smoke in smokers. Since our group will be using a stratified
sampling method, using inferential statistics just made sense
because we are trying to figure out whether or not hypnosis can
work the general populace of smokers.
Variables
A variable can be defined as an element, feature or factor that is
liable to change in quality, quantity, or size as per the
researcher’s needs. When considering an experiment, these
variables must be taken into consideration because they play
specific roles that influence the outcome of said experiment. In
a typical scientific experiment, there are three types of
variables: the independent, dependent, and control/constant
variables. The independent variable is the variable that is
manipulated by the researcher. The dependent variable is the
variable that researchers observe and measure throughout the
experiment. The control/constant variable, as the name implies,
is the variable that shouldn’t change throughout the entirety of
the experiment. The fourth variable, the extraneous variable or
the extra variables, includes all the extra variables that may
influence the outcome of said experiment. They technically
aren’t really important to the experiment and shouldn’t impact
the final outcome of experiment, but they are things that may
cause errors in the final findings due to the variables being
uncontrollable or what-not. Since our experiment is to
determine whether or not hypnosis can reduce the urge to smoke
in smokers, our variables would include the following: the
smokers/participants and the hypnotherapist/hypnosis. In this
experiment, the participants that receive the hypnotherapy
would be considered the control/constant variable, as this
variable/participant cannot change throughout the entirety of the
experiment. The independent variable would be the
hypnotherapy because this is the variable the researchers would
be introducing into the lives of the smokers/participants. The
dependent variable would be the amount cigarettes smoked by
the participants. The researchers would be observing this
variable to see whether or not if hypnosis, the independent
variable, can reduce the number of cigarettes the participants
smoke.
Operationalize the Variables
Operationalizing variable implies finding quantifiable,
valid index as well as measurable index for the variables. In
short, according to McLeod (2018), “operational variable refers
to how you will define and measure a specific variable as it is
used in your study.” The hypnosis treatment will be measured in
the context of the number of sessions that subjects undergo. We
would calculate how many sessions patients have undergone and
the length of the hypnotherapy sessions. Since our study is see
if whether or not hypnotherapy can reduce the urge in smokers
to smoke, another variable that we would need to define is the
term “reduce”. To quantify “reduce”, we must figure out how
many cigarettes each participant smokes on average in a given
time to be able to determine if hypnotherapy did or didn’t
reduce the smokers urge to smoke. We would also have to keep
not of how many cigarettes each participant smokes during the
length of the experiment. Thus, by defining these operational
variables, we are able to make clear what it is we mean by the
terms as they were studied and measured in our experiment
(McLeod, 2018).
Conclusion
In conclusion, by specifically stating the purpose of our
experiment, our modus operandi, and the intricacies of our
variables, we are able to take the next step in actually going
through with our study. Our Methods Paper is to our experiment
what an outline is to an essay. It gives us a better picture of
what our study may look like before we put our plans into
motion; thus, saving us time and allowing us to preemptively
find errors before they actually happen in our research study.
References
Centers for Disease Control Prevention. (2016). Retrieved from
https://www.cdc.gov/tobacco/data_statistics/fact_sheets/adult_d
ata/cig_smoking/index.htm
Frost, J. (2019). Statistics By Jim. Retrieved from
http://statisticsbyjim.com/basics/descriptive-inferential-
statistics/
The Economic Times(2019). Retrieved from
https://economictimes.indiatimes.com/definition/stratified-
sampling
Institutional Review Board
Application FOR HUMAN
SUBJECTS Research
The University of Phoenix Institutional Review Board (IRB)
exists to ensure university compliance with federal regulations
regarding research involving human subjects. This application
is used to facilitate and document this compliance review.
Research projects which meet the federal definition for research
and the federal definition of human subjects must be approved
by the University of Phoenix IRB before any data collection
begins. If an IRB application is approved by the IRB and, later,
the nature of the research design, requirements, or site locations
change, a revised application describing these changes must be
submitted for reconsideration and approval by the IRB. This
application is intended as a stand alone document, so reference
to other documents or appendices of dissertation proposals or
other research studies does not substitute for direct provision of
that information as part of this application, either as a response
within a section or as an addendum. This application pertains
to both pilot studies and full studies. Please note that it is the
researcher’s responsibility to give complete and accurate
information about the nature of the proposed study, particularly
in terms of the effects on, and expectations for, subject
participants. Please note that you must document currency in
CITI certification as part of this application.
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)
[city/state]
[college]
University of Phoenix
IRN: LEAVE THIS BLANK
* If research is funded, please complete the following agency
information. Otherwise, leave blank.
agency submitted to
submission date
location of project
/ /
1. Title of the Research Study/Dissertation:
2. Classification of the Study:
a) Will primary data collection from human subjects be done in
this study?
(|_|) Yes, original data only is collected from human
subjects and no archival data will be used.
(|_|) Yes, both original data from human subjects and
archival data will be collected and used.
(|_|) 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?
(|_|) Results are generalizable to a larger population.
(|_|) Results are relevant only to one organization or
entity.
3. Purpose and Anticipated Study Goal(s) and Benefits:
Briefly describe the following:
The purpose of the study:
The anticipated study goal(s):
The benefits of the study to the subjects, to the organization,
and to society:
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.)
(|_|) No (|_|) 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?
(|_|) No (|_|) 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?
(|_|) Yes (|_|) No
(|_|) 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?
(|_|) Yes, individual student data (|_|) Yes,
aggregate student data (|_|) No
(|_|) FERPA compliance (if student data is used,
please explain here and address FERPA compliance)
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? (|_|) No (|_|) Yes
d) What is the research method and design? Check all that
apply:
(|_|) quantitative analysis (|_|) qualitative analysis
(|_|) mixed methods
(|_|) phenomenological (|_|) case study (|_|)
experimental (|_|) quasi experimental (|_|) Delphi
(|_|) other (specify)
___________________________________________
e) How will data be collected? Check any that apply:
(|_|) face to face interview (|_|) focus group (|_|)
online survey (|_|) mail survey (|_|) telephone survey
(|_|) onsite survey (|_|) email survey (|_|) Skype or
related technology
(|_|) other (specify) ____________________________
f) Where will data collection occur? Check any that apply
and specify the location(s) below.
(|_|) organizational site (|_|) online (|_|) private premises (|_|)
public facility (|_|) open access site
(|_|) other (|_|) 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?
(|_|) minimal risk/stress, not greater than encountered in
ordinary daily life/activities or routine tests.
(|_|) greater than minimal risk/stress with potential for
direct benefit to the individual subjects
(|_|) 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?
(|_|) No (|_|) Yes (specify)
______________________________________
j) Will any aspect of the study take place outside of the
United States?
(|_|) No (|_|) Yes (specify where)
_______________________________________
Note that IRB approval may be needed in the country
where research is taking place.
PLEASE PROVIDE HERE (OR AS AN ADDENDUM
TO THIS APPLICATION) ANY ADDITIONAL
INFORMATION
OR EXPLANATION THAT YOU THINK MAY BE
HELPFUL TO THE IRB REGARDING YOUR RESEARCH
STUDY
DESIGN OR IMPLEMENTATION.
5. Subject Groups: Will the subjects recruited to participate in
this study include any that are in protected groups identified
below as specified within the federal human subject guidelines?
(The guidelines are defined at www.citiprogram.org)
If any category from this list is checked “yes”, please
explain in the “Comments” area below how the subjects will be
protected from harm, risk, or stress as a study participant and
how stress/risk will be mitigated or lessened.
a. Children/minors under age 18?
Yes (|_|)
No (|_|)
b. Prisoners?
Yes (|_|)
No (|_|)
c. Pregnant women?
Yes (|_|)
No (|_|)
d. Cognitively impaired or mentally
disabled?
Yes (|_|)
No (|_|)
e. Educationally or economically
disadvantaged?
Yes (|_|)
No (|_|)
Will the subjects be traumatized, comatose, or terminally ill
patients?
Yes (|_|)
No (|_|)
Will the subjects be elderly or aged persons?
Yes (|_|)
No (|_|)
Will the subjects be minorities (including women)?
Yes (|_|)
No (|_|)
Will information be withheld from subjects prior to, or during,
participation?
Yes (|_|)
No (|_|)
Will the subjects be college students?
Yes (|_|)
No (|_|)
Will the subjects be deceived, misled, or coerced in any way?
Yes (|_|)
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Will/might the subjects be students of the University of
Phoenix?
Yes (|_|)
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Will/might the subjects be faculty or staff of the University of
Phoenix?
Yes (|_|)
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Will information be requested that is, or may be, personal or
sensitive?
Yes (|_|)
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If the subjects are active duty military, will their supervisors
have influence on their participation in this research or will
participation be affected at all by the reporting relationship(s)?
Yes (|_|)
No (|_|)
Will any aspect of this study involve subjects from countries
outside of the U.S.? If yes, please specify in the comments
section below.
Yes (|_|)
No (|_|)
Comments:
6. Subject Recruitment and Selection: Briefly explain and
address the following:
a) Which of the following will be used to find and recruit
subjects? (check all that apply and include copies with
this application)
(|_|) Flyers (|_|)
Email Announcement
(|_|) Events, Meetings, Conferences (|_|) Area
Canvassing
(|_|) Phone Solicitation (|_|)
Registry
(|_|) Newspaper/Radio/Television (|_|)
Referrals from Others
(|_|) Institutional “gatekeepers” (|_|)
Direct Mail
(|_|) Face to Face Interaction (|_|)
Internet/Websites
(|_|) Bulletin Board Post (|_|)
Social Media (e.g. LinkedIn, Facebook, etc.) (please specify
(|_|) Poster
below; documented use permission is required)
(|_|)
PhoenixConnect (please note if this is used,
separate prior approval through the UOPX
Committee on Research must be documented)
(|_|) Other (please
specify)____________________________________________
EXPLAIN AND DESCRIBE HERE IF SOCIAL MEDIA
WILL BE USED ____________________________________
b) What is the anticipated sample size?
(|_|) 10 or less (|_|) 11-20 (|_|) 21-50 (|_|) 51-99
(|_|) 100-199 (|_|) 200 or more
c) Will any external parties (such as editors, translators,
interpreters, statisticians, etc.) provide assistance for
recruitment purposes? (This does not pertain to persons
who assist recruitment by “snowball sampling”.)
(|_|) No (|_|) Yes (please identify and explain
how they will assist) _____________________________
d) Are any of the research subjects students, employees, or
patients of the researcher?
(|_|) Yes (|_|) No
e) If any potential subjects under the age of 18 years are not
selected to participate in this study, what activities
will they be doing during the time the subjects are
participating in the study so that they do not feel excluded
or left out? If this scenario does not pertain to the study,
please indicate “Not applicable” here.
f) Please briefly describe the criteria that will be used to
determine the inclusion or exclusion of subjects for
this study.
g) Will any compensation or remuneration be given to
subjects for their participation in this study?
(|_|) No (|_|) Yes (please identify amount and
type, and the plan for dissemination.
PLEASE PROVIDE HERE (OR AS AN ADDENDUM TO
THIS APPLICATION) ANY ADDITIONAL INFORMATION
OR EXPLANATION CONCERNING THE ABOVE
QUESTIONS THAT YOU THINK MAY BE HELPFUL TO THE
IRB REGARDING THE RECRUITMENT OF SUBJECTS FOR
YOUR RESEARCH STUDY.
7. Informed Consent: Briefly explain and address the
following questions.
a) How will subjects be informed of the study’s purpose,
procedures, intent, duration of the study and any
potential risks or discomforts to them? Check all that
apply:
(|_|) Informed Consent form (|_|) Email (|_|) Letter
(|_|) Meeting (|_|) Phone Call (|_|) Other _______
b) How will subjects be informed of withdrawal
procedures? Check all that apply:
(|_|) Informed Consent form (|_|) Email (|_|) Letter
(|_|) Meeting (|_|) Phone Call (|_|) Other _______
c) How will the researcher contact information be provided
to the subjects? Check all that apply:
(|_|) Informed Consent form (|_|) Email (|_|) Letter (|_|)
Meeting (|_|) Phone Call (|_|) Other _______
d) How will subjects withdraw from the study as
participants after data collection is completed?
(|_|) Email the researcher (|_|) Phone call to researcher
(|_|) Submit withdrawal form
(|_|) Other (please specify)
_____________________________________________________
______
e) Please explain what subjects must do to withdraw from
the study after data is collected and how subject data
will be retrieved and handled to ensure security and
confidentiality.
f) If any subjects are under the age of 18 years, parental
consent is required. What provision is made to
answer any questions the parents have about this study or
to address any individual concerns? (For example,
will there be an informational meeting with the parents,
etc.?) If this scenario does not apply to this study,
please indicate “Not applicable” here.
PLEASE PROVIDE HERE (OR AS AN ADDENDUM TO
THIS APPLICATION) ANY ADDITIONAL INFORMATION
OR EXPLANATION THAT YOU THINK MAY BE
HELPFUL TO THE IRB REGARDING ANY OF THE ABOVE
QUESTIONS OR ABOUT THE INFORMED CONSENT
FOR YOUR RESEARCH STUDY.
PLEASE READ AND CONFIRM THROUGH CHECK
MARKING THE BOXES BELOW:
|_| I attest that no primary data collection from human
subjects will occur without a prior signed Informed
Consent form completed for each subject and that
Informed Consent documentation will be retained
separately from study data.
|_| I attest that a process for subject withdrawal will be
implemented whereby subjects may withdraw without
penalty before, during and after data collection has
been completed and submitted and that the
information they provided will be identified, secured,
withdrawn and kept confidential.
8. Confidentiality and Privacy: Briefly explain and address
how the identity and privacy of the individual subjects will be
protected. Check any of the following that apply:
a) How will subject identity and data be protected?
(|_|) Subject names will not be used or identified
(|_|) Pseudonyms or numbers will be used instead of
subject names
(|_|) Data will be coded alphanumerically
(|_|) Other (please specify)
________________________________________________
b) Will any audio and/or video tape or other recording of
data be done in this study?
(|_|) Yes (|_|) No
c) How long will the study data be kept after study
completion?
(|_|) Three years (please note this is the minimum
required retention time)
(|_|) More than three years
d) Where will the data be stored:
(|_|) In an office or other location at the researcher’s
residence
(|_|) At an office at the researcher’s place of
employment
(|_|) At a third party facility (please specify)
________________________________
(|_|) Other (please specify)
______________________________________________
e) How will data be destroyed at the appropriate time?
(|_|) Shredding (|_|) Burning or incineration
(|_|) Smashing (|_|) File Deletion
(|_|) Other (please specify)
______________________________________________
f) How will the results of this study be disseminated?
(|_|) Publication (|_|) Presentation (|_|)
Other _____________________________
PLEASE PROVIDE HERE (OR AS AN ADDENDUM TO
THIS APPLICATION) ANY ADDITIONAL INFORMATION
OR EXPLANATION CONCERNING THE ABOVE THAT YOU
THINK MAY BE HELPFUL TO THE IRB REGARDING
CONFIDENTIALITY AND PRIVACY CONCERNS
ASSOCIATED WITH YOUR RESEARCH STUDY.
PLEASE READ AND CONFIRM THROUGH CHECK
MARKING THE BOX BELOW:
|_| I attest that the data from this research will be kept in
a secured location for at least three years following
study completion, and then will be permanently
destroyed.
Current version 032012
1
Current version 032012
1
INSTITUTIONAL REVIEW
BOARD APPLICATION
FOR
HUMAN SUBJECTS
RESEARCH
The University of Phoenix Institutional Review Board (IRB
)
exists to ensure university c
ompliance
with federal regulations regarding research involving human
subjects. This application is used to
facilitate and document this compliance review. Research
projects which meet the federal
definition for research and the federal definition of hum
an subjects must be approved by the
University of Phoenix IRB before any data collection begins. If
an IRB application is approved by
the IRB and, later, the nature of the research design,
requirements, or site locations change, a
revised application desc
ribing these changes must be submitted for reconsider
ation and approval
by the IRB.
This application is intended as a stand alone document, so
reference to other
documents or appendices of dissertation proposals or other
research studies does not substitu
te
for direct provision of that information as part of this
application, either
as a
response
within a
section
or as an addendum
. This application pertains to both pilot studies and full studies.
Please note that it is the researcher’s responsibility to
give complete
and accurate
information
about the
nature of the proposed study, particularly in terms of the effects
on, and expecta
tions
for, subject participants. Please note that you must document
currency in CITI certification as
part of this applicati
on.
N
AME OF
R
ESEARCHER
(
S
)
C
ITY
,
S
TATE
,
AND
C
OUNTRY
/
S
CHOOL
OR
C
OLLEGE AND
U
NIVERSITY
A
FFILIATION
(
STUDENT
,
FACULTY
,
OR STAFF
AND ID
)
T
YPE OF
R
ESEARCH
(
RESEARCH
STUDY
,
*
FUNDED
RESEARCH
,
OR
OTHER
)
[
CITY
/
STATE
]
[
COLLEGE
]
U
NIVERSITY OF
P
HOENIX
IRN:
L
EAVE
THIS
BLANK
*
If research is funded, please complete the following
agency information
.
Otherwise, leave blank.
AGENCY SUBMITTED TO
SUBMISSION DATE
LOCATION OF PROJECT
/
/
Current version 032012
1
INSTITUTIONAL REVIEW BOARD APPLICATION
FOR HUMAN SUBJECTS RESEARCH
The University of Phoenix Institutional Review Board (IRB)
exists to ensure university compliance
with federal regulations regarding research involving human
subjects. This application is used to
facilitate and document this compliance review. Research
projects which meet the federal
definition for research and the federal definition of human
subjects must be approved by the
University of Phoenix IRB before any data collection begins. If
an IRB application is approved by
the IRB and, later, the nature of the research design,
requirements, or site locations change, a
revised application describing these changes must be submitted
for reconsideration and approval
by the IRB. This application is intended as a stand alone
document, so reference to other
documents or appendices of dissertation proposals or other
research studies does not substitute
for direct provision of that information as part of this
application, either as a response within a
section or as an addendum. This application pertains to both
pilot studies and full studies.
Please note that it is the researcher’s responsibility to give
complete and accurate information
about the nature of the proposed study, particularly in terms of
the effects on, and expectations
for, subject participants. Please note that you must document
currency in CITI certification as
part of this application.
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)
[CITY/STATE]
[COLLEGE]
UNIVERSITY OF
PHOENIX
IRN: LEAVE THIS
BLANK
* If research is funded, please complete the following agency
information.
Otherwise, leave blank.
AGENCY SUBMITTED TO SUBMISSION DATE LOCATION
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ENGLISH 2960Project #2Ethics in the Workplace A Critical Anal.docx

  • 1. ENGLISH 2960 Project #2 Ethics in the Workplace: A Critical Analysis of the film Glengarry GlenRoss *Analysis: is a process of breaking down something complex into simpler elements that will make it more understandable. *Critical Analysis: an analysis with an argumentative and evaluative edge (the writer is attempting to persuade the reader of something). For Project #2 you will apply the notion of “ethics in the workplace” to the film Glengarry GlenRoss. Further, you will write a Critical Analysis of one aspect of the movie. The direction in which you take this analysis (the aspect of the film which you analyze) is entirely up to you. I do suggest that you focus on one particular scenario (your choice) from the film that depicts an instance of unethical behavior in the workplace. Keep in mind your reading of Chapter 1, and on the below definitions of Kant's Categorical Imperative, Utilitarianism, and Ethical Relativism. I would like for you to somehow apply one of these below principles to your analysis. Length: 3 pages, typed, double-spaced. 1. Kant's Categorical Imperative: The most fundamental of all the liberal principles handed down to us from the Enlightenment and the very cornerstone of our civilization is the "categorical imperative" of Immanuel Kant: namely, that one cannot act on that maxim which one cannot will to be universal. In other words, if it's OK for me to do it, it has to be OK for everybody to do it. If it's not OK for everybody to do it, then it's not OK for me to do it either. This principle is so deeply ingrained in us, along with the contempt we feel for what we call "hypocrisy" when people violate it, that we take it for granted.
  • 2. 2. Utilitarianism: A doctrine that “the useful is the good,” and that the determining consideration of right conduct should be the usefulness of its consequences. Specifically – a theory that the aim of action should be the largest possible balance of pleasure over pain or the greatest happiness of the greatest number. 3.Ethical Relativism: In ethics,the belief that nothing is objectively right or wrong and that the definition of right or wrong depends on the prevailing view of a particular individual, culture, or historical period. _____________________________________________________ _ As you work, keep these strategies in mind: 1.) Zero in on key elements (relevant to your overall topic). 2.) View the film through a critical lens. (How are you watching and understanding this film? Through ‘political’ eyes? Through ‘social’ eyes? Through ‘psychoanalytical’ eyes?) 3.) Compare the film to something similar. (Have you read about, seen, heard of something that reminds you of the content of this film? Does something inform how you understand this film?) *Remember: For most analyses, you will utilize/use a combination of the above 3 approaches. University of Phoenix Material Proposal Worksheet Each team member will pick an article for this worksheet. Replicate these set of questions for each team member for this worksheet.
  • 3. Team member name: Kevin Hwang Citation of article: Hely, J. M., Jamieson, G. A., & Dunstan, D. (2011). Smoking Cessation: A Combined Cognitive Behavioural Therapy and Hypnotherapy Self-Help Treatment Protocol. Australian Journal of Clinical & Experimental Hypnosis, 39(2), 196–227. Retrieved from https://search- ebscohost- com.contentproxy.phoenix.edu/login.aspx?direct=true&db=a9h &AN=95317811&site=ehost-live&scope=site 1. What is the author’s goal? The author’s goal with this article was to show the efficacy of combining two forms of therapy, Cognitive Behavioral Therapy and Hypnotherapy, to help individuals to reduce cigarette intake and/or achieve cessation of smoking. 2. What questions remain unanswered? The question that still remains unanswered is if whether or not hypnosis alone can help decrease a smoker’s urge to smoke. 3. If I had to design an experiment to test this hypothesis, what would I do? If I had to design an experiment to test this hypothesis, I would have 3 separate groups. The first group would only be subject to CBT, while the second group would be subject only to Hypnotherapy. The third group would get the combined efforts of both types of therapy. 4. What are the independent, dependent, and control variables? The independent variable would be the type of therapy that is
  • 4. being administered to the group, CBT and hypnotherarpy. The dependant variable would be amount of cigarettes smoked during the experiment. The control variables would be amount of therapies that the subjects would have to undergo. Team member name:Julie Brandenburg Citation of article: Hypnotherapy for smoking cessation (Review) 2010The Cochrane Collaboration1-41 Barnes J, Dong CY, McRobbie H, Walker N, Mehta M, Stead LF 1. What is the author’s goal? The objective of this article is to figure out if hypnosis can be just as effective or even have a greater effect on quitting smoking over a six month period. The hypnosis would be compared to other interventions and verses no treatment. 2. What questions remain unanswered? Would there be a difference in the results if the individuals were looked at from a class perspective? Would someone who was poor have the same success rate as someone who had an open checkbook? 3. If I had to design an experiment to test this hypothesis, what would I do? Not only would I have chosen individuals that wanted to quit smoking and had smoked for years. I would’ve also collected the same number of women verse men and the same number of poor versus the wealthy. My objective would be to see if it’s
  • 5. easier for men or women to quit with this process. Also, if someone has the funds to invest in the hypnosis more than once would the results differ. Compared to a poor individual that wouldn’t have the funds to follow up with more sessions 4. What are the independent, dependent, and control variables? The independent variable would be the type of therapy that was used within the group study which was the hypnosis. The dependent would be the number of cigarettes that the individuals smoked during the study period. The control variable would be the number of therapy sessions that followed the hypnosis session or if there was more than one hypnosis session. Team member name: Patrice Scope Citation of article: Robinson, T. E., & Berridge, K. C. (2003). Addiction. Annual Review of Psychology, 54, 25-53 1. What is the author’s goal? The authors’ goal for this particular article was to examine the various theories about how drugs affect our psychological pathways and later turns into addictions. One of the proposed theories is a type of dysfunction on our frontol cortical systems which usually control decision making and ultimately lead to the compulsive behavior of an addiction. 2. What questions remain unanswered? Does NAcc-related circuitry play a primary role in drug addictions like drug sensitization? 3. If I had to design an experiment to test this hypothesis, what
  • 6. would I do? Hypothesis: The system NAcc-related circuitry does play a major role in drug addiction while drug sensitization plays a secondary role. To test this hypothesis, I would run various tests on drug dependent individuals (preferably, the same drug) and compare the results of the NAcc-related system to drug sensitization. The number of Dopamine receptors in the NAcc will be measured for the results. 4. What are the independent, dependent, and control variables? The independent variable would be the amount of drug. For example, the experiment could be set up on a scale with how many usages the individual partake in on a daily basis. The dependent variable would be the number of Dopamine receptors that is found in the NAcc. The control group would be a group of individuals that do not partake in drugs Team member name:Zenobia J. Bostic Citation of article:Riegel, B. Tonnies, S. (2011). Hypnosis for smoking cessation: The Effectiveness of some basic principles of hypnotherapy without using formal trace--- A Case Study. Journal Of Smoking Cessation, 6 (2), 83 – 84. doi:http://dx.doi.org.contentproxy.phoenix.edu/10.1375/jsc.6.2. 83 1. What is the author’s goal? The author’s goal to highlight some insight on some intervention strategies when using the basic principles of hypnotherapy.
  • 7. 2. What questions remain unanswered? How deep is the roots of the mental addiction of the subconscious mind(thoughts)? 3. If I had to design an experiment to test this hypothesis, what would I do? I would try to design an experiment to test “How to tap into an individual subconscious to gain knowledge of how the addiction started and what strategies from hypotherapy will connect with the habits or behavior to help them quit without the triggers. 4. What are the independent, dependent, and control variables? The independent variable was the choosing hypnosis with a high expectation of success. Dependent variable Mr. D a regular smoker for about 45 years tried to quit several times in those years. He had never stayed abstinent for more than one month. The control variable would be his motivation to quit, he spoke about the growing loneliness of smokers in today’s society. Team member name: Jennifer Ross Citation of article: Timothy P. Carmosy, Carol Duncan, Joel A. Simons, Sharon Solkowitz, Joy Huggins, Sharon Lee, Kevin Delucchi; Hypnosis for Smoking Cessation: A Randomized Trial, Nicotine & Tobacco Research, Volume10, Issue 5, 1 May 2008, Pages 811-818,https://doi- org.contentproxy.phoenix.edu/10.1080/14622200802023833 1. What is the author’s goal? The goal of this article was to determine whether hypnosis is more effective in helping smokers quit then just regular
  • 8. behavior counseling. 2. What questions remain unanswered? The question I have is does hypnosis alone help smokers quit. 3. If I had to design an experiment to test this hypothesis, what would I do? I would set up different test subjects. Some with just hypnosis, and the same number getting both behavior couseling and hypnosis. I would see the status of all groups in 7 to 10 10 days then again at 3 months, 6 months, 9 month, and one year. 4. What are the independent, dependent, and control variables? independent variable is behavioral counciling, dependent is hypnosis only group, control would be hypnosis. After reviewing each team member’s submission, answer the following questions as a team: 1. What is your research question? How can hypnosis help smokers decrease their urge to smoke? 2. What is your hypothesis? Since studies show that hypnosis can be used to alter automatic mental processes, individuals who undergo hypnotherapy will see a decrease in urge to smoke. 1
  • 9. 3 Methods PaperLearning Team APSY/335 February 4th, 2019 Brian Claybrook Methods Paper As previously discussed during our proposal assignment in Week Two, the area of research we chose to focus on revolves around question and hypothesis of whether or not hypnosis could help smokers decrease their urge to smoke. In this paper, we will discuss our sampling methods, the type of statistics, descriptive or inferential, we will use, definitions of our variables, and how we will operationalize said variables. The purpose of this Methods Paper is so that we, as a team, can show how to properly set up and execute a research study. Sampling Method The sampling method that we choose to go with was the stratified sampling method. A stratified sampling method refers to a methodology where researchers divide a total population into smaller groups known as strata. According to The Economic Times (2019), “strata are formed based on some common characteristics in the population data.” After the population is divided into strata, the researchers would then randomly select the sample from each group. In 2016, it was determined that 37.8 million Americans smoke in the United States. Since our team wanted to get a sample that gave us true and unbiased data without having a humongous group, we decided to take a look at the nation’s smoking population. According to the data collected by the CDC from a survey conducted in 2016, there were more men than women smokers, by four percent. Thus, we choose to select a hundred adults, 54% men and 46% women. Out of the current number of smokers, it had been polled that 18% were of the ages 45 to 64, 17% were 25 to 44, and the remain 13% were 18 to 24 years old (Centers for Disease Control Prevention, 2016). Having this
  • 10. information, we decided to make strata according to gender as well as age. From there, we will take samples from each stratum to create a proportionally random sampling group to test our hypothesis on. Descriptive or Inferential Statistics For this study, our group decided to use inferential statistics. The reasoning behind this was because inferential statistics revolves around the concept that the data collected from the sample will be used to make inferences about the larger population from which the sample was drawn from (Frost, 2019). In layman’s terms, this means that the data that will be collected from the research will be used to make a general claim regarding the subject matter. In the case of our study, depending on what the study shows, we may say that our findings show us that the hypnosis may or may not possibly reduce the urge to smoke in smokers. Since our group will be using a stratified sampling method, using inferential statistics just made sense because we are trying to figure out whether or not hypnosis can work the general populace of smokers. Variables A variable can be defined as an element, feature or factor that is liable to change in quality, quantity, or size as per the researcher’s needs. When considering an experiment, these variables must be taken into consideration because they play specific roles that influence the outcome of said experiment. In a typical scientific experiment, there are three types of variables: the independent, dependent, and control/constant variables. The independent variable is the variable that is manipulated by the researcher. The dependent variable is the variable that researchers observe and measure throughout the experiment. The control/constant variable, as the name implies, is the variable that shouldn’t change throughout the entirety of the experiment. The fourth variable, the extraneous variable or the extra variables, includes all the extra variables that may
  • 11. influence the outcome of said experiment. They technically aren’t really important to the experiment and shouldn’t impact the final outcome of experiment, but they are things that may cause errors in the final findings due to the variables being uncontrollable or what-not. Since our experiment is to determine whether or not hypnosis can reduce the urge to smoke in smokers, our variables would include the following: the smokers/participants and the hypnotherapist/hypnosis. In this experiment, the participants that receive the hypnotherapy would be considered the control/constant variable, as this variable/participant cannot change throughout the entirety of the experiment. The independent variable would be the hypnotherapy because this is the variable the researchers would be introducing into the lives of the smokers/participants. The dependent variable would be the amount cigarettes smoked by the participants. The researchers would be observing this variable to see whether or not if hypnosis, the independent variable, can reduce the number of cigarettes the participants smoke. Operationalize the Variables Operationalizing variable implies finding quantifiable, valid index as well as measurable index for the variables. In short, according to McLeod (2018), “operational variable refers to how you will define and measure a specific variable as it is used in your study.” The hypnosis treatment will be measured in the context of the number of sessions that subjects undergo. We would calculate how many sessions patients have undergone and the length of the hypnotherapy sessions. Since our study is see if whether or not hypnotherapy can reduce the urge in smokers to smoke, another variable that we would need to define is the term “reduce”. To quantify “reduce”, we must figure out how many cigarettes each participant smokes on average in a given time to be able to determine if hypnotherapy did or didn’t reduce the smokers urge to smoke. We would also have to keep not of how many cigarettes each participant smokes during the
  • 12. length of the experiment. Thus, by defining these operational variables, we are able to make clear what it is we mean by the terms as they were studied and measured in our experiment (McLeod, 2018). Conclusion In conclusion, by specifically stating the purpose of our experiment, our modus operandi, and the intricacies of our variables, we are able to take the next step in actually going through with our study. Our Methods Paper is to our experiment what an outline is to an essay. It gives us a better picture of what our study may look like before we put our plans into motion; thus, saving us time and allowing us to preemptively find errors before they actually happen in our research study. References Centers for Disease Control Prevention. (2016). Retrieved from https://www.cdc.gov/tobacco/data_statistics/fact_sheets/adult_d ata/cig_smoking/index.htm Frost, J. (2019). Statistics By Jim. Retrieved from http://statisticsbyjim.com/basics/descriptive-inferential- statistics/ The Economic Times(2019). Retrieved from https://economictimes.indiatimes.com/definition/stratified- sampling Institutional Review Board Application FOR HUMAN SUBJECTS Research The University of Phoenix Institutional Review Board (IRB) exists to ensure university compliance with federal regulations
  • 13. regarding research involving human subjects. This application is used to facilitate and document this compliance review. Research projects which meet the federal definition for research and the federal definition of human subjects must be approved by the University of Phoenix IRB before any data collection begins. If an IRB application is approved by the IRB and, later, the nature of the research design, requirements, or site locations change, a revised application describing these changes must be submitted for reconsideration and approval by the IRB. This application is intended as a stand alone document, so reference to other documents or appendices of dissertation proposals or other research studies does not substitute for direct provision of that information as part of this application, either as a response within a section or as an addendum. This application pertains to both pilot studies and full studies. Please note that it is the researcher’s responsibility to give complete and accurate information about the nature of the proposed study, particularly in terms of the effects on, and expectations for, subject participants. Please note that you must document currency in CITI certification as part of this application. 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) [city/state] [college] University of Phoenix IRN: LEAVE THIS BLANK
  • 14. * If research is funded, please complete the following agency information. Otherwise, leave blank. agency submitted to submission date location of project / / 1. Title of the Research Study/Dissertation: 2. Classification of the Study: a) Will primary data collection from human subjects be done in this study? (|_|) Yes, original data only is collected from human subjects and no archival data will be used. (|_|) Yes, both original data from human subjects and archival data will be collected and used. (|_|) 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? (|_|) Results are generalizable to a larger population.
  • 15. (|_|) Results are relevant only to one organization or entity. 3. Purpose and Anticipated Study Goal(s) and Benefits: Briefly describe the following: The purpose of the study: The anticipated study goal(s): The benefits of the study to the subjects, to the organization, and to society: 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.) (|_|) No (|_|) Yes (Please describe here)
  • 16. 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? (|_|) No (|_|) 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? (|_|) Yes (|_|) No (|_|) 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? (|_|) Yes, individual student data (|_|) Yes, aggregate student data (|_|) No (|_|) FERPA compliance (if student data is used, please explain here and address FERPA compliance)
  • 17. 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? (|_|) No (|_|) Yes d) What is the research method and design? Check all that apply: (|_|) quantitative analysis (|_|) qualitative analysis (|_|) mixed methods (|_|) phenomenological (|_|) case study (|_|) experimental (|_|) quasi experimental (|_|) Delphi (|_|) other (specify) ___________________________________________ e) How will data be collected? Check any that apply: (|_|) face to face interview (|_|) focus group (|_|) online survey (|_|) mail survey (|_|) telephone survey (|_|) onsite survey (|_|) email survey (|_|) Skype or related technology
  • 18. (|_|) other (specify) ____________________________ f) Where will data collection occur? Check any that apply and specify the location(s) below. (|_|) organizational site (|_|) online (|_|) private premises (|_|) public facility (|_|) open access site (|_|) other (|_|) 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? (|_|) minimal risk/stress, not greater than encountered in ordinary daily life/activities or routine tests. (|_|) greater than minimal risk/stress with potential for direct benefit to the individual subjects (|_|) 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? (|_|) No (|_|) Yes (specify) ______________________________________ j) Will any aspect of the study take place outside of the
  • 19. United States? (|_|) No (|_|) Yes (specify where) _______________________________________ Note that IRB approval may be needed in the country where research is taking place. PLEASE PROVIDE HERE (OR AS AN ADDENDUM TO THIS APPLICATION) ANY ADDITIONAL INFORMATION OR EXPLANATION THAT YOU THINK MAY BE HELPFUL TO THE IRB REGARDING YOUR RESEARCH STUDY DESIGN OR IMPLEMENTATION. 5. Subject Groups: Will the subjects recruited to participate in this study include any that are in protected groups identified below as specified within the federal human subject guidelines? (The guidelines are defined at www.citiprogram.org) If any category from this list is checked “yes”, please explain in the “Comments” area below how the subjects will be protected from harm, risk, or stress as a study participant and how stress/risk will be mitigated or lessened. a. Children/minors under age 18? Yes (|_|) No (|_|) b. Prisoners? Yes (|_|)
  • 20. No (|_|) c. Pregnant women? Yes (|_|) No (|_|) d. Cognitively impaired or mentally disabled? Yes (|_|) No (|_|) e. Educationally or economically disadvantaged? Yes (|_|) No (|_|) Will the subjects be traumatized, comatose, or terminally ill patients? Yes (|_|) No (|_|) Will the subjects be elderly or aged persons? Yes (|_|) No (|_|) Will the subjects be minorities (including women)? Yes (|_|) No (|_|) Will information be withheld from subjects prior to, or during, participation? Yes (|_|) No (|_|) Will the subjects be college students? Yes (|_|)
  • 21. No (|_|) Will the subjects be deceived, misled, or coerced in any way? Yes (|_|) No (|_|) Will/might the subjects be students of the University of Phoenix? Yes (|_|) No (|_|) Will/might the subjects be faculty or staff of the University of Phoenix? Yes (|_|) No (|_|) Will information be requested that is, or may be, personal or sensitive? Yes (|_|) No (|_|) If the subjects are active duty military, will their supervisors have influence on their participation in this research or will participation be affected at all by the reporting relationship(s)? Yes (|_|) No (|_|) Will any aspect of this study involve subjects from countries outside of the U.S.? If yes, please specify in the comments section below. Yes (|_|) No (|_|) Comments:
  • 22. 6. Subject Recruitment and Selection: Briefly explain and address the following: a) Which of the following will be used to find and recruit subjects? (check all that apply and include copies with this application) (|_|) Flyers (|_|) Email Announcement (|_|) Events, Meetings, Conferences (|_|) Area Canvassing (|_|) Phone Solicitation (|_|) Registry (|_|) Newspaper/Radio/Television (|_|) Referrals from Others (|_|) Institutional “gatekeepers” (|_|) Direct Mail (|_|) Face to Face Interaction (|_|) Internet/Websites (|_|) Bulletin Board Post (|_|) Social Media (e.g. LinkedIn, Facebook, etc.) (please specify (|_|) Poster below; documented use permission is required) (|_|) PhoenixConnect (please note if this is used,
  • 23. separate prior approval through the UOPX Committee on Research must be documented) (|_|) Other (please specify)____________________________________________ EXPLAIN AND DESCRIBE HERE IF SOCIAL MEDIA WILL BE USED ____________________________________ b) What is the anticipated sample size? (|_|) 10 or less (|_|) 11-20 (|_|) 21-50 (|_|) 51-99 (|_|) 100-199 (|_|) 200 or more c) Will any external parties (such as editors, translators, interpreters, statisticians, etc.) provide assistance for recruitment purposes? (This does not pertain to persons who assist recruitment by “snowball sampling”.) (|_|) No (|_|) Yes (please identify and explain how they will assist) _____________________________ d) Are any of the research subjects students, employees, or patients of the researcher? (|_|) Yes (|_|) No e) If any potential subjects under the age of 18 years are not selected to participate in this study, what activities will they be doing during the time the subjects are participating in the study so that they do not feel excluded or left out? If this scenario does not pertain to the study, please indicate “Not applicable” here.
  • 24. f) Please briefly describe the criteria that will be used to determine the inclusion or exclusion of subjects for this study. g) Will any compensation or remuneration be given to subjects for their participation in this study? (|_|) No (|_|) Yes (please identify amount and type, and the plan for dissemination. PLEASE PROVIDE HERE (OR AS AN ADDENDUM TO THIS APPLICATION) ANY ADDITIONAL INFORMATION OR EXPLANATION CONCERNING THE ABOVE QUESTIONS THAT YOU THINK MAY BE HELPFUL TO THE IRB REGARDING THE RECRUITMENT OF SUBJECTS FOR YOUR RESEARCH STUDY. 7. Informed Consent: Briefly explain and address the following questions. a) How will subjects be informed of the study’s purpose, procedures, intent, duration of the study and any potential risks or discomforts to them? Check all that apply: (|_|) Informed Consent form (|_|) Email (|_|) Letter (|_|) Meeting (|_|) Phone Call (|_|) Other _______ b) How will subjects be informed of withdrawal procedures? Check all that apply: (|_|) Informed Consent form (|_|) Email (|_|) Letter
  • 25. (|_|) Meeting (|_|) Phone Call (|_|) Other _______ c) How will the researcher contact information be provided to the subjects? Check all that apply: (|_|) Informed Consent form (|_|) Email (|_|) Letter (|_|) Meeting (|_|) Phone Call (|_|) Other _______ d) How will subjects withdraw from the study as participants after data collection is completed? (|_|) Email the researcher (|_|) Phone call to researcher (|_|) Submit withdrawal form (|_|) Other (please specify) _____________________________________________________ ______ e) Please explain what subjects must do to withdraw from the study after data is collected and how subject data will be retrieved and handled to ensure security and confidentiality. f) If any subjects are under the age of 18 years, parental consent is required. What provision is made to answer any questions the parents have about this study or to address any individual concerns? (For example, will there be an informational meeting with the parents, etc.?) If this scenario does not apply to this study, please indicate “Not applicable” here. PLEASE PROVIDE HERE (OR AS AN ADDENDUM TO THIS APPLICATION) ANY ADDITIONAL INFORMATION
  • 26. OR EXPLANATION THAT YOU THINK MAY BE HELPFUL TO THE IRB REGARDING ANY OF THE ABOVE QUESTIONS OR ABOUT THE INFORMED CONSENT FOR YOUR RESEARCH STUDY. PLEASE READ AND CONFIRM THROUGH CHECK MARKING THE BOXES BELOW: |_| I attest that no primary data collection from human subjects will occur without a prior signed Informed Consent form completed for each subject and that Informed Consent documentation will be retained separately from study data. |_| I attest that a process for subject withdrawal will be implemented whereby subjects may withdraw without penalty before, during and after data collection has been completed and submitted and that the information they provided will be identified, secured, withdrawn and kept confidential. 8. Confidentiality and Privacy: Briefly explain and address how the identity and privacy of the individual subjects will be protected. Check any of the following that apply: a) How will subject identity and data be protected? (|_|) Subject names will not be used or identified (|_|) Pseudonyms or numbers will be used instead of subject names (|_|) Data will be coded alphanumerically (|_|) Other (please specify) ________________________________________________
  • 27. b) Will any audio and/or video tape or other recording of data be done in this study? (|_|) Yes (|_|) No c) How long will the study data be kept after study completion? (|_|) Three years (please note this is the minimum required retention time) (|_|) More than three years d) Where will the data be stored: (|_|) In an office or other location at the researcher’s residence (|_|) At an office at the researcher’s place of employment (|_|) At a third party facility (please specify) ________________________________ (|_|) Other (please specify) ______________________________________________ e) How will data be destroyed at the appropriate time? (|_|) Shredding (|_|) Burning or incineration (|_|) Smashing (|_|) File Deletion (|_|) Other (please specify) ______________________________________________ f) How will the results of this study be disseminated? (|_|) Publication (|_|) Presentation (|_|) Other _____________________________ PLEASE PROVIDE HERE (OR AS AN ADDENDUM TO THIS APPLICATION) ANY ADDITIONAL INFORMATION OR EXPLANATION CONCERNING THE ABOVE THAT YOU THINK MAY BE HELPFUL TO THE IRB REGARDING CONFIDENTIALITY AND PRIVACY CONCERNS ASSOCIATED WITH YOUR RESEARCH STUDY.
  • 28. PLEASE READ AND CONFIRM THROUGH CHECK MARKING THE BOX BELOW: |_| I attest that the data from this research will be kept in a secured location for at least three years following study completion, and then will be permanently destroyed. Current version 032012 1 Current version 032012 1 INSTITUTIONAL REVIEW BOARD APPLICATION FOR HUMAN SUBJECTS RESEARCH
  • 29. The University of Phoenix Institutional Review Board (IRB ) exists to ensure university c ompliance with federal regulations regarding research involving human subjects. This application is used to facilitate and document this compliance review. Research projects which meet the federal definition for research and the federal definition of hum an subjects must be approved by the University of Phoenix IRB before any data collection begins. If an IRB application is approved by the IRB and, later, the nature of the research design, requirements, or site locations change, a revised application desc ribing these changes must be submitted for reconsider ation and approval by the IRB. This application is intended as a stand alone document, so reference to other documents or appendices of dissertation proposals or other research studies does not substitu te for direct provision of that information as part of this application, either as a response within a section or as an addendum . This application pertains to both pilot studies and full studies. Please note that it is the researcher’s responsibility to
  • 30. give complete and accurate information about the nature of the proposed study, particularly in terms of the effects on, and expecta tions for, subject participants. Please note that you must document currency in CITI certification as part of this applicati on. N AME OF R ESEARCHER ( S ) C ITY , S TATE , AND C OUNTRY /
  • 33. * If research is funded, please complete the following agency information . Otherwise, leave blank. AGENCY SUBMITTED TO SUBMISSION DATE LOCATION OF PROJECT / /
  • 34. Current version 032012 1 INSTITUTIONAL REVIEW BOARD APPLICATION FOR HUMAN SUBJECTS RESEARCH The University of Phoenix Institutional Review Board (IRB) exists to ensure university compliance with federal regulations regarding research involving human subjects. This application is used to facilitate and document this compliance review. Research projects which meet the federal definition for research and the federal definition of human subjects must be approved by the University of Phoenix IRB before any data collection begins. If an IRB application is approved by the IRB and, later, the nature of the research design, requirements, or site locations change, a revised application describing these changes must be submitted for reconsideration and approval by the IRB. This application is intended as a stand alone document, so reference to other documents or appendices of dissertation proposals or other research studies does not substitute for direct provision of that information as part of this application, either as a response within a section or as an addendum. This application pertains to both pilot studies and full studies.
  • 35. Please note that it is the researcher’s responsibility to give complete and accurate information about the nature of the proposed study, particularly in terms of the effects on, and expectations for, subject participants. Please note that you must document currency in CITI certification as part of this application. 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) [CITY/STATE] [COLLEGE] UNIVERSITY OF PHOENIX IRN: LEAVE THIS BLANK
  • 36. * If research is funded, please complete the following agency information. Otherwise, leave blank. AGENCY SUBMITTED TO SUBMISSION DATE LOCATION OF PROJECT / /