An Internet-Based Study H-100 Form
Application for Human Research Review H-100
Colorado State University
This information will assist you in applying for approval to use human participants for research under Colorado State University’s auspices. All of the information is available on the Regulatory Compliance Web page, .
Under the Federal Policy for the Protection of Human Subjects, Federal Register, V. 56, No. 117, June 18, 1991, and later amendments, Colorado State University’s Human Research Committee (HRC) is required to review and approve all proposed research involving humans that is conducted under the University’s auspices. Approval is required regardless of funding status or sponsorship. Our campus policies are affirmed to the federal government in a document titled “Federalwide Assurance of Compliance with DHHS Regulations for Protection of Human Research Subjects” (1996, copy available on the Web page or by request).
The main considerations and responsibilities of the HRC are to determine that
a. the potential risks to research subjects are adequately addressed and their confidentiality is assured.
b. adequate explanation of the potential risks and safeguards, as well as benefits, are given to the subjects and their consent to participate is validated.
c. the proposals are clearly planned and the risk/benefit ratio to the subjects is clearly articulated and acceptable.
Philosophically, the HRC believes that investigators who use humans in their studies have a fundamental ethical responsibility to inform the participants of the nature of the investigation and obtain informed consent for participation in the studies. The procedure for obtaining informed consent may differ from one study to another, but using a carefully considered procedure has the advantage that it will reduce problems for the investigator in the future. Participants who have a clear understanding of the extent and purpose of their role in a study are less likely to have complaints about the investigator and the study. The fundamental right of individuals to be informed of their role in research should not be violated by investigators, and should be of particular concern to all involved in conducting research involving human participation. Failure of even one researcher to abide by ethical guidelines could jeopardize the future right of everyone at the University to conduct research.
The Administrator for the HRC is a staff person (see below) with the Regulatory Compliance Office, located at 410 University Services Center. All inquiries, correspondence, and submissions should be directed there.
A current copy of the curriculum vitae of the Principal Investigator must be on file in the Administrator’s office. If you have submitted a vitae since July 1 of this year, you do not need to include it with this application.
If this project is being conducted for a graduate degree, the student’s faculty advisory committee should approve it before it is submitted to the HRC. The faculty Principal Investigator will receive the original review and approval documentation; the student will receive copies through his/her campus department address. Renewal documents will be sent to the Principal Investigator only, since the student typically has graduated. It is the responsibility of the Principal Investigator to retain records and report the status of the project for renewal or close-out.
Data from human subjects are not to be collected until approval is received from the Human Research Committee.
Training of the PI:
A protocol may be reviewed, but not approved, until the Principal Investigator has successfully completed one of CSU’s human research protection training options and met any continuing education requirements. This became a requirement with CSU’s 2001 Federalwide Assurance. Details about training are linked from the human research web site at www.research.colostate.edu/rcoweb.
How to proceed:
1. Become familiar with this packet. Consult other links on the Human Research web page (FAQ and tips especially).
2. Complete Parts A, B, C & D. This must be done for all types of review. Include all necessary attachments.
3. Preliminarily determine the type of review for which your project would qualify (the final determination rests with the HRC and any project may be referred to the HRC for full review at a regularly convened meeting). If you have questions about the type of review for which your project will qualify, call the HRC Administrator in the Regulatory Compliance Office (see below).
• Exempt Review: See Exemption Criteria. Submit anytime. Submit the original application. Keep a copy for yourself. Reviewed by one reviewer. Response in approximately 10 days.
• Expedite Review: See Expedite Criteria. Submit anytime. Submit the original application and one entire copy (but only one copy of the proposal/prospectus and résumé). Keep a copy for yourself. Reviewed by two reviewers. Response in approximately 14 days.
• Full Review: Every other type of activity. Submit by noon on second Thursday of every month. Submit the original application and 13 entire copies (but only one copy of the proposal/prospectus and résumé). Keep a copy for yourself. Reviewed by full HRC at regular monthly meeting on the third Thursday of every month. Response is within 10 business days after committee meeting.
Remember: Each application set represents your project to the HRC reviewer. It must be complete.
Submit application and copies to:
410 University Services Center
After review, you will receive an e-mail or printed determination notice (copy to the student co-PI via campus mail to the department) outlining the reviewers' concerns. Once the concerns have been satisfactorily addressed, a written approval notice will be sent to both the researcher and the student Co-PI. Federal certification forms will be provided if the project is being submitted for funding to a federal agency requiring such forms (USDA, NIH).
Recognizing every situation has unique characteristics, please do not hesitate to call the Administrator if you have questions or concerns: Janell Meldrem, HRC Administrator. Telephone: 970-491-1655 FAX: 970-491-2293 E-mail: firstname.lastname@example.org.
2. Forms to be completed: Application to Use Human Subjects H-100
Part A: Cover page.
Part B: Research Project Review Summary.
Part C: Protocol information, to be typed on your word processor in Word. Every question must be answered, even if "not applicable."
Part D: Special requirements/attachments checklist. Don’t forget a copy of the entire proposal or prospectus.
3. Helpful information All of these are available separately on the HRC Forms web site.
a. Exempt criteria
b. Expedite criteria
c. Risks of common procedures (focus groups, blood draws, etc.)
e. Elements of a consent form
f. Model consent form. If your project will require a consent form, remove the italics, bracketed
text from this model and add project-specific information to produce a consent form that is
typically suitable for a routine project.
For best results, save this as a file to your computer. If bullets or different formatting are needed, unprotect the file.
Office Use Only: HRC Tracking number: _____________
Type of Review: ? Exempt ? Expedite ? Full Category #_______ PI Trained Y ? N?
APPLICATION FOR Human subjects research review
COLORADO STATE UNIVERSITY
(Please type or electronically fill)
Complete the cover page, review summary, and sections A, B, C & D. For full review protocols, submit the ORIGINAL (with original signatures and copy of proposal/dissertation/thesis) and 13 copies (each with attachments except proposal/dissertation/thesis) to Regulatory Compliance Office (RCO), 410 University Services Center, Campus Delivery 2011. Assistance is available on the RCO web site at http://www.research.colostate.edu/rcoweb
H-100 COVER SHEET Part A
Project Title (identical to proposal or thesis/dissertation): Faith, Identity and the Rhetoric of the Emergent Church Online
Grant Title if different from Project Title:
Principal Investigator (PI):
Name: Sarah Jane Sloane
Campus Mailing Address & Mail Code: 359 William O. Eddy Hall (1773)
Phone #: 970-491-2816
E-Mail Address: email@example.com
Co-Investigator (attach information if more than one Co-PI):
Name: Jennifer Stewart
Campus Mailing Address & Mail Code: 266 Aylesworth Hall (1773)
Phone #: 970-491-4573
E-Mail Address: firstname.lastname@example.org
Proposed Start Date (may not precede approval date):
X “Upon HRC approval”
If Co-PI is a student, is this project for a:
X thesis dissertation other
I think this qualifies for the following type of review:
Exempt Category number (submit original)
X Expedite Category number 7 (submit original & one copy)
Full Review (submit original & 13 copies)
New Protocol XYES NO
Resubmission YES X NO
Follow-up to 118 request YES X NO
As the PI submitting this proposed research and signing below, I agree to conduct the research involving human subjects as presented in the protocol or modifications to it and as approved by the Department and the Human Research Committee; to obtain and document informed consent and provide a copy of the consent form to each subject unless this is waived by the HRC; to present any proposed modifications in the research to the HRC for review and approval prior to implementation; to retain records for the mandated lengths of time; and to report to the HRC any problems or injuries to subjects.
PI Signature: _____________________________________________ Date: __________________
My signature below confirms that I have read this protocol and approve of this research.
Department Chair/Head or Acting Signature
Signature:____________________________________________ Date: ___________________
(If PI is Department Head, please have alternate/designee sign)
PART B. RESEARCH PROJECT REVIEW SUMMARY Your completion of the following checklist will facilitate the review process.
1. SUBJECT POPULATION: (Check all appropriate boxes.)
Healthy adults X Children or minors (<18)
Institutional residents Cognitively or psychologically impaired
Elderly Pregnant women or fetuses
Prisoners or parolees Non-English speaking
2. If the research involves any of the following, check the appropriate boxeS:
Clinical studies Behavioral observation
Investigational drugs Investigational devices
Deception X Waiver of consent
XStudy of existing data Controlled substances
Study of human biological specimens Microorganisms or recombinant DNA
Venipuncture Genetic research
PI or Co-PI is the treating physician
3. LOCATION(S) OF RESEARCH TO BE CONDUCTED AT:
XCSU campus X Other locations, specify: Online materials may be accessed from off-campus locations
4. INFORMED CONSENT OF SUBJECTS: Your study protocol must clearly address one of the following areas: (justification for #2 & #3 must be included in your application) Discuss details in purpose section, (question If).
INFORMED CONSENT: Signed informed consent is the default. A model consent is available on the HRC website and should be used as a basis for developing your informed consent document. If applicable, the proposed consent must be submitted with the study protocol. http://www.research.colostate.edu/rcoweb/hr/hr_forms.htm
COVER LETTER: You may request a waiver of documented informed consent under the following conditions: (1) That the only recording linking the subject and the research would be the consent document and the principle risk would be potential harm resulting from a breach of confidentiality. Each subject will be asked whether the subject wants documentation linking the subject with the research, and the subject’s wishes will govern; (45CFR46.117c1), OR (2)That the research presents no more than minimal risk of harm to subjects and involves no procedures for which written consent if normally required outside of the research context. (45CFR46117c2).
It is the responsibility of the investigator to: a) provide clear justification for how a
project meets the criteria for waiver of documented informed consent under one of the
two previous categories, and b) provide what will be used to inform the subjects about research activities. It may be a telephone or verbal script, a cover letter, or some other means.
The cover letter needs to be sent to the subjects and to the HRC on CSU departmental letterhead.
X NO INFORMED CONSENT: You may request a waiver of informed consent under the following conditions: (1) The research involves no more than minimal risk to the subjects; (2) the waiver or alteration will not adversely affect the rights and welfare of the subjects; (3) the research could not practicably be carried out without the waiver or alteration; and (4) when appropriate, the subjects will be provided with additional pertinent information after participation (45CFR46.116d).
It is the responsibility of the investigator to: a) explain how a project meets all four of the criteria for waiver of informed consent and b) where applicable, provide an alternate form of sharing study information with prospective subjects (i.e., a public service announcement, or a modified version of a consent to be used in research that by design requires deception – this type of research requires an accompanying debriefing form that completes the informed consent process).
PART C. RESEARCH PROTOCOL:
I. PURPOSE, METHODS, AND PROCEDURES: Describe the following:
a. Purpose (will be used in assessing the risk/benefit ratio for subjects. The hypothesis to be tested may be listed.) The project is designed to answer our central research question about currently used rhetoric of specfic online communities, known as the "emergent" or "emerging" church, and their members. The research questions are as follows: How do emergent religious communities online use language and linguistic practices to construct their beliefs, purposes and identities rhetorically? And, what are the distinguishing characteristics of the rhetoric of this movement or group?
b. Research methods and procedures of the study. (It is OK to diagram complex designs. Please include information on the time commitment required for each activity.) To conduct our study of “emergent Christian religious communities,” we will investigate the language used and statements made within a number of online community websites that have identified themselves as “emergent” or “postmodern.” The project will focus on analysis of texts produced by writers who participate in conversations (electronically) surrounding the issues of postmodernism and the future of the Christian faith. Because both group and individual articulations of religious identity exist, we will read both individual texts and mission statements. Therefore, two types of textual data will be collected for this project. The first type consists of mission statements from four websites associated with the emergent church movement: www.emergentvillage.com, www.ginkworld.net, www.the-next-wave.org, and www.theooze.com. Each of these sites has a statement of “who we are,” or “about us” that describes the beliefs and goals of each site respectively. These materials are publicly accessible from each main homepage and can be considered public domain documents. The second type of online text that will be collected will consist of threads and individual postings to the message boards on www.theooze.com. Within this site, we will read and collect distinct threads of conversation and then analyze the discussions of topics/issues that are of interest. (For example: postmodernity, identity, “emergence,” certain oft-repeated metaphors, etc.) These exact categories will probably become more evident after further reading, and will be determined by our thread selection criteria. No direct interaction, intervention or communication with the authors of the texts will take place. Our study will focus solely on the textual data, not its authors. Thus, to protect the anonymity of the posters (further discussion follows), we will replace each screen name with a pseudonym. This will mean keeping a list of each unique screen name and providing a counterpart before any data are used or included in the write-up of the project. This list will be discarded one year after the project is complete, approximately May 2006. We will read postings to the online boards periodically (two to three times weekly for a period of six weeks), copying and dating messages of interest. These documents can be discarded at the end of the project as well, although most information gathered will continue to be available through the archives of the online sites being investigated. The collected texts, then, reflect the writing of individual authors, as well as the statements of several prominent organizations within the emergent movement. We will evaluate whether individual writers indeed mirror the concerns and rhetoric used by the broader organizations, or if there is a lack of connection between the language of the movement’s participants and those who act as its spokespersons. The intersection of these distinct points of articulation will reveal how this movement conceives of itself, both at the individual and community level.
c. Variables to be studied (what is being measured or examined). In this rhetorical analysis, the variables will be textual. As explained above, we will isolate distinct categories of discussion within these message boards and mission statements, including common metaphors, topics or other tropes or terms.
d. Describe equipment used with subjects, if any. No equipment will be used with subjects. Because the site of inquiry will be computer-based, though, it can be presumed that all subjects will have access and familiarity with computer systems, message boards and other types of online activities.
e. How will subject confidentiality or anonymity be maintained? If a linked list is used, list when it will be destroyed. Provide a sample of the code that will be used. To protect each author's anonymity, we will replace each posted screen name with a pseudonym. Using guidelines suggested by the Association of Internet Researchers in its paper on "Ethical decision-making and Internet Research"(2002), we will keep a list of each screen name and provide an alternate name before any data are used or included in the write-up of the project. This list will be discarded one year after the project is complete, approximately May 2006.
f. Describe the consent process and method of consent to be used. (signed consent, cover letter, other) No Informed Consent (justifications attached)
g. How will research records be maintained during and upon completion of the project? (This may include audio or videotapes). Indicate when the records and/or tapes will be destroyed. Federal Regulations require that study data and consent documents be kept for a minimum of 3 years after the completion of the study by the PI; for longitudinal projects, a longer period may be needed.
Records for this project will consist of 1) mission statements posted on the four selected websites, and 2) individual postings to message boards, which will be saved electronically as Word documents. To protect the anonymity of each text's author (as described above), we will replace each screen name with a pseudonym. This will mean keeping a list of each screen name and providing an alternate name before any data are used or included in the write-up of the project. This will provide another level of protection to the anonymity of the author, in addition to the anonymity afforded by the screen name. This list will be discarded one year after the project is complete, approximately May 2006. We will read postings to the online boards periodically (two to three times weekly for a period of six weeks), copying and dating messages of interest (as determined by my selection criteria). These documents can be discarded at the end of the project as well, although most information gathered will continue to be available through the archives of the online sites being investigated.
h. Address how you will monitor this study to ensure that the study is being conducted according to the protocol. Ms. Stewart will meet weekly with Dr. Sloane to insure protocols are continuing to be followed and to review any unforeseen ethical or practical problems. Discussion with Dr. Sloane, the Principal Investigator, will be ongoing throughout the research process in order to maintain consistent data collection.
i. Is a Data Safety Monitoring Board required to conduct such monitoring? YES NO
If yes, the HRC may request copies of the reports.
II. SUBJECT SELECTION: Indicate the following (this section must also be completed for secondary data analysis):
a. How will subjects be recruited and where will the recruitment take place? (submit recruitment material) The topic of subject recruitment pertains to the second type of textual data we will collect - postings made to online message boards. Because these types of texts are produced by individual authors and then posted to message boards at a chosen website (www.theooze.com), no real selection of “subjects” will occur. Once these texts are submitted to the message boards at the chosen site, the text becomes the object of analysis, and texts will be selected on the basis of their content. All identifying information about the author will be removed from the text being analyzed. As stated elsewhere, no demographic information about the author will be collected, as the focus of our investigation is not upon the authors themselves but on the texts which they create.
b. If secondary data analysis is being conducted, please describe the original consent procedures. No secondary data analysis is being conducted.
c. What are the characteristics of the subject population? (age, gender, student, disease conditions, behavioral abnormalities; affiliations or memberships) In order to protect the authors' anonymity, we will not collect demographic information, neither from individuals nor from the website as a whole. The only known affiliation/membership that can be assumed is that, because they must register with the website theooze.com in order to post to its message boards, they have some affiliation with or interest in the topics discussed within www.theooze.com.
d. How many subjects do you plan to study? The total number of individual posters/contributors will range from 5 to around 50.
e. Address the inclusion and exclusion criteria. Federal regulations consider minors, pregnant women and prisoners vulnerable populations that require added protection. When vulnerable populations are involved, describe why they are necessary. Excluding any group, i.e., minors, elderly, gender, ethnic minorities, must be clearly justified and inconvenience can’t be the reason. For example, if minors are in a classroom where recruitment will take place, parental permission must be obtained or justification must be made to exclude the minors. Texts posted to the message boards under investigation will be included or excluded based on evolving textual selection criteria; therefore, individual authors/subjects are included or excluded on the basis of the content of the texts they have posted. Because demographic information will not be connected to the text collected, it will not be possible to determine if authors are or are not members of vunerable population groups.
f. Will subjects be compensated for participation? If so, please describe the proposed compensation. No
g. Criteria for excluding participants involuntarily (such as “failed to keep food diary as required”) Partcipant texts will be excluded if unrelated to the linguistic and rhetorical categories under investigation.
h. Letters of agreement/approval from the organizations that will be recruiting subjects for the project will be needed. Such letters need to be initiated by the organization, on organization letterhead, and signed by a person authorized to do so. The letters need to include statements a) that the organization is familiar with the scope of the project, b) that it is satisfied the individuals it is involving are adequately protected as human research subjects, c) that the subjects’ participation is completely voluntary, and d) identify what the organization’s involvement will entail.
III. RISKS AND DISCOMFORTS:
a. Describe any potential risks to subjects and assess the likelihood and seriousness of those risks. (If there are no known risks, state as such, but do NOT respond “NA”.) These could include: physical, psychological trauma or stress, legal, social, economic, loss of confidentiality. The only known risk to authors involved in this study is the loss of anonymity. Precautions previously discussed make this unlikely.
b. Please describe the proposed methods to minimize the risks and discomforts associated with the research. For example, document how potential psychological distress will be addressed, by whom, and with what credentials (provide letter of agreement from counselor explaining their role – this must be someone other than the researchers on the project) Specify what factors will lead to stopping procedures causing physical or emotional stress. The anonymity of each author will be maintained by using pseudonyms in place of the individual's screen name, providing another level of protection to the anonymity of the author, in addition to the anonymity afforded by the screen name.
c. If the methods of research create potential risks, describe other methods, if any, that were considered and why they will not be used. We believe the given protocols for this type of research are sufficient to minimze the risks involved.
d. Address procedures for maintaining confidentiality if a breach of confidentiality represents a risk. Again, the anonymity of each author will be maintained by using pseudomyms in place of the individual's screen name. This will mean keeping a list of each unique screen name and providing a counterpart before any data are used or included in the write up of the project. This list will be discarded one year after the project is complete, approximately May 2006.
IV. ADVERSE EVENTS: Explain your reporting mechanism for reporting adverse and serious adverse events to the HRC. In this type of qualitative research study, we anticipate no adverse or serious events related to the study. If in the unlikely event that a serious event occurs, Dr. Sloane will immediately contact Celia Walker, Director of Regulatory Compliance.
V. BENEFITS: Describe the anticipated benefits of the research to the individual subjects, to the particular group or class from which the subject population is drawn. The benefits must be realistic and not overly stated of what each person is likely to gain from the research. If there is no direct benefit to the subject, state so. For example: “There is no known benefit in participating in this study, but we hope you will gain more knowledge on…” Compensation, payment for participation, gifts, etc., are NOT benefits. There are no direct benefits to the participants of the study, but the eventual findings may be of interest to the creators of the websites under study, as well as to the wider "emerging church" community, both on the web and the local church setting.
VI. Other matters pertinent to the human participant. There are no other matters pertinent to the human participant.
Part D. SPECIAL REQUIREMENTS/ATTACHMENTS CHECKLIST: For the items below, check where applicable and include with your protocol submission. Items marked “required” must accompany an HRC protocol application or the project can not be approved.
Research Proposal Materials
Grant proposal (if this is a funded project, this is required)
Thesis/dissertation methods (if the project is a thesis or dissertation, this is required)
CV (If this is a first time submission as PI, this is required. A current copy of the curriculum vitae of the PI must be on file in the Administrator’s office. If the PI has submitted a vitae since July 1 of the current year, the PI does not need to include it with this application).
Informed Consent, or
X Cover letter (with justification for waiver), or
X Justification for waiving informed consent
Interviews (phone or in person) - attach script if applicable and questions to be asked.
Surveys/questionnaires - attach surveys and questionnaires if applicable. Provide permission use for instruments (whether copyrighted or public domain)
X Focus Groups: attach introductory script to the group and sample questions. (describe in consent form what a focus group is)
Recruitment materials: Advertisements, press releases, in-class announcements, posted flyers, e-mail announcements, phone script, or other forms of recruitment.
Research Collaboration/Support Materials
IRB approval from other institutions involved in research (collaborating university, hospital, etc.)
Letters of cooperation from participating sites that do not have an IRB.
Letters of agreement (i.e., from a site that is allowing you access, but is not directly involved in research, or a colleague allowing you to recruit from a class, a clinic or business allowing recruitment, etc.)
X Letter of collaboration from a counselor if needed.
Secondary Data Analysis (for research involving secondary data analysis, include original IRB approval and informed consent)
X IRB approval from collaborating organization
X Consent form from original data analysis