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CONSENT FORM Can open label placebos augment an existing online treatment for insomnia? Principal Investigator: Professor Keith Metric Student Researcher: Sasha Finlay Investigator: Professor Lee
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What is consent form can open-label?
Consent form can open-label is a document that allows researchers to disclose the treatment that participants are receiving during a clinical trial.
Who is required to file consent form can open-label?
Researchers conducting a clinical trial are required to file the consent form can open-label.
How to fill out consent form can open-label?
The consent form can open-label should be filled out by including all relevant treatment information and obtaining signatures from participants.
What is the purpose of consent form can open-label?
The purpose of consent form can open-label is to ensure that participants are informed about the treatment they are receiving during a clinical trial.
What information must be reported on consent form can open-label?
The consent form can open-label must include details about the treatment, potential risks, benefits, and any other relevant information.
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