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BIOMEDICAL RESEARCH ALLIANCE OF NEW YORK LLC SYRACUSE UNIVERSITY SUBJECT INFORMATION AND INFORMED CONSENT FORM Protocol Title: BiofeedbackEnhanced Treatment for Speech Sound Disorder: Randomized Controlled

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What is rct informed consent form?

RCT informed consent form is a document that provides information to participants about the risks and benefits of participating in a randomized controlled trial.

Who is required to file rct informed consent form?

Researchers conducting a randomized controlled trial are required to obtain and file informed consent forms from all participants.

How to fill out rct informed consent form?

The rct informed consent form should be filled out by the researcher or healthcare professional conducting the trial, and should include information about the study objectives, procedures, risks, benefits, and participant rights.

What is the purpose of rct informed consent form?

The purpose of rct informed consent form is to ensure that participants are fully informed about the study before agreeing to participate, and to protect their rights and safety.

What information must be reported on rct informed consent form?

The rct informed consent form must include information about the study objectives, procedures, risks, benefits, participant rights, confidentiality, and contact information for the researcher.

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