???? ????? Name and Title Dept. Phone, E-mail address 3. Non-key personnel: ????? ????? Name and Title Dept. Phone, E-mail address 7. Consultants: ????? ????? Name and Title Dept. Phone, E-mail address 8. The principal investigator agrees to carry out the proposed project as stated in the application and to promptly report to the Human Subjects Committee any proposed changes and/or unanticipated problems involving risks to subjects or others participating in approved project in accordance with the Liberty Way and the Confidentiality Statement. The principal investigator has access to copies of 45 CFR 46 and the Belmont Report. The principal investigator agrees to inform the Human Subjects Committee and complete all necessary reports should the principal investigator terminate association with the University. Additionally s/he agrees to maintain records and keep informed consent documents for three years after completion of the project even if the principal investigator terminates association with the University. ___________________________________ _________________________________________ Principal Investigator Signature Date ___________________________________ _________________________________________ Faculty Sponsor (If applicable) Date Submit the original request to: Liberty University Institutional Review Board, CN Suite 1582, 1971 University Blvd., Lynchburg, VA 24502. Submit also via email to firstname.lastname@example.org APPLICATION TO USE HUMAN RESEARCH SUBJECTS 10. This project will be conducted at the following location(s): (please indicate city & state) Liberty University Campus X Other (Specify): Charlottesville High School: Charlottesville, Virginia 11. This project will involve the following subject types: (check-mark types to be studied) X Normal Volunteers (Age 18-65) Subjects Incapable Of Giving Consent In Patients Prisoners Or Institutionalized Individuals Out Patients X Minors (Under Age 18) Patient Controls Over Age 65 Fetuses University Students (PSYC Dept. subject pool __) Cognitively Disabled Other Potentially Elevated Risk Populations______ Physically Disabled __________________________________________ Pregnant Women Subjects Incapable of Giving Consent. 12. Do you intend to use LU students, staff or faculty as participants in your study? If you do not intend to use LU participants in your study, please check “no” and proceed directly to item 13. YES NO X If “Yes”, please list the department and/or classes you hope to enlist and the number of participants you would like to enroll. ????? In order to process your request to use LU subjects, we must ensure that you have contacted the appropriate department and gained permission to collect data from them. Signature of Department Chair: ___________________________________ ____________________________ Department Chair Signature(s) Date 13. Estimated number of subjects to be enrolled in this protocol: ___15-25____________ 14. Does this project call for: (check-mark all that apply to this study) X Use of Voice, Video, Digital, or Image Recordings? Subject Compensation? Patients $????? Volunteers $????? Participant Payment Disclosure Form Advertising For Subjects? More Than Minimal Risk? More Than Minimal Psychological Stress? Alcohol Consumption? X Confidential Material (questionnaires, photos, etc.)? Waiver of Informed Consent? Extra Costs To The Subjects (tests, hospitalization, etc.)? VO2 Max Exercise?
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(Application to Use Human Research Subjects Essay)
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11/06 Ref. # _ APPLICATION TO USE HUMAN RESEARCH SUBJECTS Liberty University Committee On The Use of Human Research Subjects 1. Project Title: Understanding the Experiences of Special Education Students who did not Complete High School. 2. Full Review Expedited Review X 3…
Please note that we can only accept our forms in Microsoft Word format. In addition, please submit one signed copy of the fourth page of the protocol form, which is the Investigator’s Agreement. Also submit the second page if a departmental signature is required for your study.
The author presents a working definition of the term Neurofeedback, followed by some background information of the technique as it is used in the medical field. The report then presents a detailed discussion of the technique highlighting its clinical effectiveness as a therapeutic measure in training patients to overcome their problematic conditions and probably improve their performances.
Such collaboration is not possible if all (participants and the researcher) are not on the same page. Collaboration will ensure accountability and responsiveness. Research ethics demands that participants have necessary information before embarking on the research study.
Studies involving human tissue samples are central to biomedical research. Human tissue-based models are important to understand the vital proteomic and genomic differences that occur in human disease that will help develop proper diagnostic tools and treatments.
In many clinical trials, the majority of research subjects enrolled are white males. However, this is not representative of the entire U.S. population, which is comprised of other ethnic groups, like the 'African American' and the other minorities.
Therefore, the million dollar question is, is the primary enrolment of white males into clinical trials consistent with the ideal of a fair and equitable selection process that ensures a fair distribution of the burdens as well as the benefits of research This article on the unequal representation of the entire component of the U.S.
But the available literature identifies bullying as often repeated incidents or the regular pattern of bahaviour of an individual intended to intimidate, offend or degrade or humiliate a fellow worker or a group of workers. The term bullying also cover the negative body contact as well.
The use of animals has been widespread across the world for the medical research and testing. There are a lot of health hazards and diseases which can be tested only on living beings. Before developing any treatment, the researchers have the duty of detecting the health problems associated with it.
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