A Toolkit for Redesign in Health Care: Final Report
Form H. Staff Member Consent Form
You are being asked to take part in a research study that is looking at ways to improve the way hospitals work and provide care to patients. You are being asked to be in this study because you are a medical staff member at _______________, where this study is taking place. You will be observed for the duration of your shift in the hospital. We will document where you go in the hospital and how long you stay there. We will also document the medical care you provide, the people you communicate with, and other tasks performed. The duration of these events will also be documented.
Up to _____ local subjects will be enrolled in this research study.
If you agree to take part in this study, your duties during you shift will not be changed in any way. We will ask you to read and sign this consent form only. From this point on, we will observe your movements throughout the hospital until the end of your shift. The information collected that could identify you on an individual basis will be kept in our records until ____________ and during this time will be kept confidential. You are being asked to be in this study because you are clinical staff that provides direct patient care in the _________________ Department.
Discomforts and Risks
The study may include risks that are unknown at this time.
This study is designed for the researcher to learn more about improving hospital care. This study is not designed to treat any illness or to improve your health.
The sponsor for this study is the _________________________________________________________.
Cost to Subject
There is no cost to you for participating in this study. You will not be paid for participation in this study.
Voluntary Participation and Study Withdrawal
Taking part in this study is voluntary.You have the right to choose not to take part in this study. If you do not take part in the study, your doctor will still take care of you.You will not lose any benefits or medical care to which you are entitled. If you choose to take part, you have the right to stop at any time.If there are any new findings during the study that may affect whether you want to continue to take part, you will be told about them. The study doctor may decide to stop your participation without your permission, if he or she thinks that being in the study may cause you harm, or for any other reason. Also the sponsor may stop the study at any time.
Invitation for Questions
The researcher carrying out this study is __________________. You may ask any questions you have now. If you have questions later, you may call ____________ at (___)___-____. You will be given a copy of this form to keep.
If you have questions regarding your rights as a research subject, please call the Institutional Review Board office at (___)___-____.
We will try to keep your research records confidential, but it cannot be guaranteed. Records that identify you (including your medical records) and the consent form signed by you, may be looked at by the following people:
The results of this research may be presented at meetings or in published articles. However, your name will be kept private. You will also be asked to sign a separate authorization form. This form will explain who will have access to your protected health information.
Injury and Compensation
You should inform your care provider(s) if you decide to participate in this research study. If you have questions about injury related to the research, you may call ________________ at (___)___-____ and/or your private physician. ________________ should be informed about any injury you experience while you take part in this study.
I have read this paper about the study or it was read to me. I understand the possible risk and benefits of this study. I know that being in this study is voluntary. I choose to be in this study. I know I can stop being in this study and I will still get the usual medical care. I will get a copy of this consent form. (Initial all the previous pages of the consent form).
Print Name (subject) ____________________ Date ___________
Consent form explained by: __________________________________________
Print Name _________________ Date ___________
Investigator ______________________________ Date ______________