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STUDY INFORMED CONSENT The Combined Effects of Prolonged Sitting and Mental Stress on Vascular and Cerebrovascular Function in Mileage Adults NCT number NCT04207333 Consent Form Version Date: 12/05/19IRB
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Step 1: Read the study informed consent form carefully to understand its purpose and requirements.
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Step 2: Provide all the necessary personal information requested in the form, such as your name, age, contact details, etc.
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Step 3: Make sure to ask any questions or seek clarification regarding the study or the consent form before signing it.
04
Step 4: Review all the risks and benefits associated with participating in the study as outlined in the informed consent form.
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Step 5: If you agree to participate in the study and understand the risks involved, sign and date the informed consent form.
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Step 6: Keep a copy of the signed informed consent form for your records.

Who needs study informed consent?

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Anyone who is considering participating in a research or study project needs to fill out a study informed consent.
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This includes individuals of any age, gender, or background, as long as they meet the criteria set by the study organizers.
03
Minors or individuals with legal guardians may require additional consent from their parents or guardians.
04
Researchers and study organizers also need study informed consent from participants to ensure transparency and ethical compliance.
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Study informed consent is a process in which a participant voluntarily confirms their willingness to participate in a research study after being informed of all aspects that might influence their decision. This includes information about the study's purpose, procedures, risks, and potential benefits.
Researchers and institutions conducting studies that involve human participants are required to file study informed consent to ensure ethical standards are met and participants are fully informed.
To fill out study informed consent, researchers should provide clear information about the study, including its purpose, procedures, risks, benefits, and the right to withdraw. Participants need to sign the document to confirm their understanding and agreement.
The purpose of study informed consent is to protect participants’ autonomy and ensure that they make informed decisions regarding their involvement in a research study, thereby safeguarding their rights and well-being.
The informed consent document must include details about the study's purpose, procedures, risks, benefits, confidentiality, compensation, and contact information for questions or concerns.
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