[Contractor Facility]
Informed Consent for Participants of Investigative Projects
Title of Project: Evaluation of the Degree of Enhanced Visibility of Pedestrians and Traffic Control Devices under Various Vision Enhancement Systems
Investigators: [List Name of Investigators Here]
THE PURPOSE OF THE PROJECT IS TO DETERMINE THE DEGREE OF ENHANCED VISIBILITY OF THE ROADWAY ENVIRONMENT WITH VARIOUS TYPES OF VISION ENHANCEMENT SYSTEMS WHILE DRIVING AT NIGHT.
The primary risks that you may come into contact with are the obstacles on the road for Study 3. It is for this reason that you are to maintain a speed of not more than 25 miles per hour (this will be maintained for all three studies) and to maintain a 200-foot area between the vehicle and the obstacles (only applies to Study 3). For your safety, the following precautions are taken:
While there are no direct benefits to you from this research (other than payment), you may find the experiment interesting. No promise or guarantee of benefits is made to encourage you to participate. Your participation will help to improve the body of knowledge regarding various vision enhancement systems.
The data gathered in this experiment will be treated with confidentiality. Shortly after you have participated, your name will be separated from your data. A coding scheme will be employed to identify the data by participant number only (e.g., Participant No. 3). After the experiment, the data will be kept in a locked safe.
You will be paid 20 dollars per hour for participating in this study. You will be paid in cash at the end of your voluntary participation in this study.
As a participant in this research, you are free to withdraw at any time without penalty. If you choose to withdraw, you will be compensated for the portion of time of the study for which you participated. Furthermore, you are free not to answer any question or respond to experimental situations without penalty.
Before data can be collected, the research must be approved, as required, by the Institutional Review Board for Research Involving Human Subjects at [name of contractor review board]. You should know that this approval has been obtained.
If you voluntarily agree to participate in this study, you will have the following responsibilities:
I have read and understand the Informed Consent and conditions of this project. I have had all my questions answered. I hereby acknowledge the above and give my voluntary consent for participation in this project.
If I participate, I may withdraw at any time without penalty. I agree to abide by the rules of this project.
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Signature Date
Should I have any questions about this research or its conduct, I may contact: (List names and contact information for review board and investigators here).
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