Complete IRB Application Assignment
Purpose: Complete an IRB Application based on your research study.
Instructions: For this assignment, When conducting research, it is important to get approval from an IRB committee. You may also have to create an informed consent if you involving any human participants in your study. Both of the templates are provided to you below.
What Documentation is needed for the IRB Application?
These are the major sections of the IRB Application Form:
Principal Investigator (You)
Faculty Member overseeing your research project Department/Program Affiliation
Project Title “The Leadership Behavior and Job Satisfaction Within The HIM”
Description of the research
Description of the participants (if using secondary dataset – please describe here)
Description of procedures involving participants (if using secondary dataset, this is N/A)
Description of risks and discomforts to the participates (if using secondary dataset, this is N/A)
Description of the means to minimize each risk or violation above (if using secondary dataset, this is N/A)
Consent to be used (Consent Form Example – attached).
Copies of affiliation letters or permissions
Name of professional documents that will guide your ethical responsibilities (such as http://ethicscodescollection.org/detail/317dc831-f558-4b49-ae8e-069314c331ae
Informed Consent
If you are required to create an Informed Consent, the following must be included (see sample above)
Informed Consent Basic Elements
Provide the information needed to help a potential participant make an informed decision about whether to participate. Information should be presented in sufficient detail and organized and presented in a way that facilitates a subject’s understanding of why one might or might not want to participate. Avoid using technical terms.
Consent forms should include the following basic elements:
Name of the college should appear at the top of the form;
Provide the title of the project;
Indication of the investigator’s status, i.e., faculty, graduate student, undergraduate student; if a student, provide the name of your mentor;
Description of the purpose of study in non-technical terms;
Description of all tasks the participant will be asked to perform; include an accurate estimate of the length of time needed to participate;
Information about risks and steps taken to minimize those risks;
Information about potential benefits to the participant;
Alternatives to participating in the study;
A statement clearly indicating that participation is voluntary and the subject’s right to withdraw at any time;
Notification of steps taken to protect the personal identity of participants and confidentiality of data;
Include contact information (name, title, phone) for the current Dean of the School and Department Chair affiliated with the research; provide the name and contact information for the Chair of the Institutional Review Board;
Lines for participant’s and researcher’s name, signature, and date (except electronic surveys);
A statement indicating that a copy of the consent form will be provided to the participant;
For research involving physical risks, a statement as to availability or non-availability of treatment for illness or injuries resulting from the research must be provided.
Requirements:
Complete entire IRB Application using the following application: IRB Application (attached).
Complete informed consent if there are human participants using the following form: Sample Consent Form
Format: Submit the assignment in a word document. Your paper should be formatted following APA 7 Guidelines.
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