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DoD IRB NUMBER: WRNMMC20190232 IRB APPROVAL DATE: 06/28/2019 IRB EXPIRATION DATE: 06/27/2020(DM001) Version # 1.1, Date: 08 May 2019 Walter Reed National Military Medical Center Consents TO PARTICIPATE
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Step 1: Read the consent form carefully.
02
Step 2: Provide your personal information such as name, age, and contact details.
03
Step 3: Understand the purpose and objectives of the research or project.
04
Step 4: Ask any questions or seek clarification from the researcher if needed.
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Step 5: Sign the consent form indicating your voluntary participation.
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Step 6: Keep a copy of the signed consent form for your records.

Who needs consent to participate in?

01
Anyone who is going to participate in a research study, experiment, clinical trial, survey, or any other type of project that requires human subjects to provide data, opinions, or engage in any activities.
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Consent to participate in is a form signed by an individual agreeing to take part in a specific activity or program.
Any individual who wishes to participate in a particular activity or program that requires formal consent.
Consent to participate in can be filled out by providing personal information, signing the form, and agreeing to the terms and conditions of participation.
The purpose of consent to participate in is to ensure that individuals are aware of the risks and requirements of the activity or program they are participating in.
Consent to participate in typically includes information about the individual's personal details, emergency contact information, and any relevant medical conditions.
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