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IRB Approved Protocol, Consent and Statistical Plan : Title: Can transcranial direct current stimulation improve ambulation and fatigue resistance in people with MS? NCT #: NCT02987621 Document date:

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What is irb approved protocol consent?

IRB approved protocol consent is a document that outlines the details of a research study and the informed consent process that participants must go through before taking part in the study.

Who is required to file irb approved protocol consent?

Researchers conducting studies that involve human subjects are required to file IRB approved protocol consent.

How to fill out irb approved protocol consent?

To fill out IRB approved protocol consent, researchers must follow the guidelines provided by the Institutional Review Board (IRB) and include all necessary information about the study and the informed consent process.

What is the purpose of irb approved protocol consent?

The purpose of IRB approved protocol consent is to ensure that participants are fully informed about the risks and benefits of participating in a research study and that their rights and welfare are protected.

What information must be reported on irb approved protocol consent?

Information reported on IRB approved protocol consent includes details about the study purpose, procedures, risks, benefits, confidentiality measures, and participant rights.

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