ࡱ> WYV 0bjbjr r .``_`_(8 8 11111EEE8} 4E#==MMM(((l#n#n#n#n#n#n#W& )Zn#1(((((n#11MM# (|1M1Ml# (l# Z]h8 X##0# g)D<g) 8g)1 d(( (((((n#n#<(((#((((g)(((((((((8 : Application form: Expedited Review Investigators (including faculty sponsor): Department/Program: Name of Project: Directions: Expedited review is appropriate when research does not qualify for limited review but does not require full review. First check the application form for limited review to see if your project qualifies. If you believe expedited review is appropriate, please check all applicable items in Parts A and B and provide all relevant information in Part C. Research activities will only be considered for expedited review when all items in Part A and at least one item in Part B apply. PART A: 1. ______ The research does not involve prisoners, fetuses, pregnant women, the seriously ill, or mentally or cognitively compromised adults as subjects.(Note: research with prisoners may be considered for expedited review when the research only incidentally includes prisoners as part of a broader population. Research on incarcerated people that focuses on their status as prisoners is not eligible for expedited review.) 2. ______ The procedures of this research present no more than minimal risk to the subject (where minimal risk means that the probability and magnitude of harm or discomfort anticipated in the proposed research are no greater than those ordinarily encountered in daily life or during the performance of routine physical/psychological examinations or tests). 3. ______ Either the research requires subjects to provide informed consent prior to participating or the research qualifies for Category 1 in Part B below and does not involve the collection of identifiable information. PART B (Check all categories that apply to your research project) please underline or highlight the relevant portion(s) of the chosen bullet points) 1. ____ Collection of data through use of the following procedures: a) non-invasive procedures routinely employed in clinical practice excluding procedures involving x-rays or microwaves; b) physical sensors that are applied either to the surface of the body or at a distance and do not involve input of significant amounts of energy into the subject or an invasion of the subject's privacy; c) weighing, testing sensory acuity, electrocardiography, electroencephalography, thermography, detection of naturally occurring radioactivity, electroretinography, echography, sonography, ultrasound, magnetic resonance imaging (MRI), diagnostic infrared imaging, doppler blood flow, and echocardiography; d) moderate exercise, muscular strength testing, body composition assessment, and flexibility testing where appropriate given the age, weight, and health of the individual. 2. ____ Collection of data from voice, video, digital or image recordings made for research purposes where identification of the subjects and/or their responses would not reasonably place them at risk of criminal or civil liability, be stigmatizing, or be damaging to the subjects' financial standing, employability, insurability, or reputation and where the research is not eligible for limited review. 3. ____ Research on individual or group characteristics or behavior (including but not limited to research involving perception, cognition, motivation, identity, language, communication, cultural beliefs or practices, and social behavior, or research employing surveys, interviews, oral history, focus groups, program evaluation, human factors evaluation, or quality assurance methodologies) and where the research is not eligible for limited review. 4. ____ Research involving the use of educational tests (cognitive, diagnostic, aptitude, achievement), survey procedures, interview procedures, or observation of public behavior and where the research is not eligible for limited review. 5. ____ Research that involves deception and participants do not consent to being deceived in the informed consent procedure [NOTE: Deception must be scientifically justified and de-briefing procedures must be outlined in detail. Based upon the judgment of the reviewers, some protocols involving deception may qualify for expedited review. In other cases, the deception will be of sufficient consequence to require full IRB review.] 6. ____ Prospective collection for research purposes of biological specimens; research on drugs or devices for which an investigational new drug exemption or an investigational device exemption is not required; and collection of blood samples by finger stick or venipuncture. 7. ____ Research previously approved by the convened IRB as follows: (a) where (i) the research is permanently closed to the enrollment of new subjects; (ii) all subjects have completed all research-related interventions; and (iii) the research remains active only for long-term follow-up of subjects; or (b) where the research remains active only for the purposes of data analysis; or (c) where the IRB has determined at a convened meeting that the research involves no greater than minimal risk and no additional risks have been identified; or (d) where no subjects have been enrolled and no additional risks have been identified. PART C Please provide the following information. Compose your responses within the form. Please avoid the use of abbreviations. 1. What is the purpose of the proposed study (the research question) and what is the research hypothesis? [Note: This is basically the introduction to your paper, not just a one-sentence purpose. It will likely be one paragraph to one page long, and should be grounded in the literature.] 2. Describe the proposed subject sample. If subjects under the age of 18 will participate in your research, indicate the samples expected age range. For 91˶Ƶ students who are not yet 18 years old, please send them to the IRB chair to obtain parental consent. 3. How will subjects be recruited and selected? 4. Describe fully the following: (a) all research methods and procedures that will be employed in this study. What will subjects be required to do as part of their participation in this study? [This section should be a page or so long this is the meat of what youll be doing in your study.] b) approximately how much time each subject is expected to devote to the research. (c) how personal information and research data will be collected and recorded: (1) Personal information. Either describe how and where you will collect and store any information that could be used to connect subjects identities with the collected data (considering that subjects may be identifiable through combinations of demographic information like age, race, nationality, etc.) or clearly state that the research will not collect any data that could be used to identify the subject. (2) Research data. Describe all instruments, materials, and/or equipment will be used to collect data. Append copies of all written instruments and/or describe any apparatus with which subjects will be in direct contact.If you are proposing an online study, please provide the link to the full study, in addition to including the study information in this proposal. (d) methods for obtaining informed consent (for subjects age 18 years or older) or assent (for minors). For minors, indicate how the consent of parents or legal guardians will also be obtained. Append copies of all materials used to obtain informed consent or assent. Model forms may be found at Forms and Instructions. e) methods for preserving confidentiality. This includes both plans for keeping subjects identity separated from research data and plans for storing/disposing of tapes and other data records at the conclusion of the research (such as storing data or recordings in your private files or computer and any plans to post data to a public repository, e.g., Open Science Framework). f) if deception is to be employed, provide a scientific justification for its use and describe debriefing procedures. Explain to them what your hypothesis is, what your experimental manipulations were. This should also include your contact information and how/where the subjects can see the results of the study that they participated in. [NOTE: If the research is such that debriefing cannot be carried out, the project must be submitted for full committee review.] 5. Indicate any benefits that are expected to accrue to subjects as a result of their participation in the research (this can include the subjects gaining knowledge on facts in the field, or the subjects learning about how the field gains its knowledge). In the event that subjects will be paid (in money or Psychology SONA credits), describe all payment arrangements, including how much subjects will be paid should they choose to withdraw from the study prior to completion of the research. Note that the IRB expects mTurk subjects (or other online workers; Prolific expects at least $12/hr) to be paid at a rate at or above Indianas minimum wage. Also note that partial compensation is unfortunately not really feasible on mTurk or Prolific, so partial subjects there will have to either be fully compensated or not compensated for their time. 6. Describe any relationship between researcher and subjects that could make potential subjects vulnerable to undue influence or coercion (e.g., fraternity member/pledge, teacher/student; superintendent/principal/teacher, employer/employee). If such a relationship exists, how will the researcher ensure that subjects register for and complete the research without coercion or influence from the researcher. Appendices: Please append to this document any additional information that is applicable, including consent forms, survey instruments, etc. Please make certain that surveys are easily legible: font at least 11 point, scans not faint or blurry. Sample in person or online study consent forms are available on the 91˶Ƶ IRB website. Please compile this information into a single MS Word document. Also include a copy of the certificate of completion for the CITI online human subjects certification training program for each of the researchers. (Please submit the certificate, not the listing of grades on each module.) For student projects, also include a scanned signed Research Review Declaration. The CITI certificates and Research Review Declaration should be in their own files, separate from the proposal. References Please include a reference section, including any cited works.     PAGE  #$%12NPQcefxyN _ a f v ~  󸧖tbTTTTTTTTTTThCJOJQJ^JaJ#hh2hd->*CJOJQJ^JaJ hh2hICJOJQJ^JaJ hh2h# CJOJQJ^JaJ hh2h. CJOJQJ^JaJ hh2hCJOJQJ^JaJ hh2hd-CJOJQJ^JaJhh2hh25OJQJ\^Jhh2hd-5OJQJ\^Jhh2OJQJ^Jhh2hd-OJQJ^J$%Qfxyd e n   ^`bc $da$gdymP $ !a$gdymP$h9D[$\$^ha$gd'> $h9D^ha$gd9$9D[$\$a$gd'>$a$gdymP$a$gd@3 < ? b d e l m n S    ? 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