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Trial Outcomes for Massage: Care AllyAssisted vs. TherapistTreated (TOMCATT) NCT 03100539 JUNE 27, 2022Department of Veterans AffairsVA Research Consent FormSubject Name:Date:Title of Study:Trial

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What is template for informed consent?

A template for informed consent is a standardized form used to inform participants about the details of a study or procedure, ensuring they understand any risks, benefits, and their rights before consenting to participate.

Who is required to file template for informed consent?

Researchers conducting studies involving human subjects are required to file a template for informed consent.

How to fill out template for informed consent?

To fill out a template for informed consent, researchers should provide clear information about the study's purpose, procedures, risks, benefits, confidentiality, and what participation involves, as well as obtain signatures from participants.

What is the purpose of template for informed consent?

The purpose of a template for informed consent is to ensure that individuals understand what they are agreeing to when participating in research or clinical trials, thereby protecting their autonomy and rights.

What information must be reported on template for informed consent?

The template must include the study's purpose, procedures, duration, potential risks and benefits, confidentiality assurances, contact information for questions, and a statement regarding voluntary participation.

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