Consent Form

Attachment 8-Consent form.doc

National Amyotrophic Lateral Sclerosis (ALS) Registry

Consent Form

OMB: 0923-0041

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Attachment 8

Consent Form


Background – ALS is the most common motor neuron disease which causes the deterioration of the upper and motor neuron. Motor neurons send signals to the muscles. There are a lot of questions about the number of people who have ALS and what causes it.


Purpose – The purpose of this research is to get a better picture of who gets ALS or other motor neuron diseases. The information could also be used to design studies about what causes ALS. You are being asked to take part because you have ALS. If you decide to register, you will be asked for information about you and where you live. If you take part in any of the survey modules, you will be asked to answer some questions about who you are, where you lived or worked, family history of ALS, and how you are coping with your diseases. You will only be asked to answer most questions one time. You will be asked to complete questions on how you are coping with your ALS twice a year. The survey modules can be done whenever you want. You can do them all at once or over a period of time.


Risks – The major risk of taking part is someone getting your information. To keep this from happening, we will limit who can see your information. We will also have computer security that keeps your information safe.


Benefits – There are no direct benefits to you. In the future, your information could help others with ALS.


Confidentiality – Your information will be kept confidential to the extent allowed by law. Only authorized individuals will have access to your information. Your information will be stored in a secure location with limited access. Any information that is published about people in the registry will not identify you.


Results – The website where you registered will have reports about what we learn from people who take part in the National ALS Registry and surveys.


Voluntary – Taking part is up to you. You do not have to take part and you can stop taking part at any time. You will not lose any benefits to which you are entitled if you do not take part or chose to quit.


If you have any questions about the surveys, you can contact Dr. Oleg Muravov at XXX. If you have any questions about your rights as a research participant you can contact XXX.


By clicking on ACCEPT, if you agree to take part in the surveys.


 Accept – (Go to list of Surveys)

 Reject – (Go to ALS registry home page)


Flesch-Kincaid Reading Level 7.5

File Typeapplication/msword
File TitleAttachment 8
Authorwek1
Last Modified Bywek1
File Modified2009-11-24
File Created2009-11-24

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