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    • 30 Day Gratitude Protocol
    • 30 Day Gratitude Protocol

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    • Jules Mann-Stewart
    • Create & Run Clinical Studies
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    What You Need to Know to Participate

    This document provides information to help you decide whether to join this research study. It is important you understand the responsibilities, risks and benefits of participating.

    Research Informed Consent Form
    Title of Study: [Insert Study Title Here]
    Principal Investigator(s): [Investigator Name(s) and Contact Information]
    Institution/Organization: [Organization Conducting the Research]
    Date: [Insert Date]


    Purpose of the Study

    You are being invited to participate in a research study. The purpose of this study is to [briefly explain the study's purpose in plain language].

    What Participation Involves

    If you agree to participate, you will be asked to:

    • [Describe activities or procedures involved, e.g., complete a survey, participate in an interview, or provide a sample].
    • The total time commitment will be approximately [insert time duration].

    Voluntary Participation

    Participation in this study is entirely voluntary. You may choose not to participate or withdraw from the study at any time without penalty or loss of benefits to which you are otherwise entitled.

    Risks and Benefits

    • Risks: [Describe any risks involved, even if they are minimal. If no significant risks are present, state this clearly.]
    • Benefits: [Describe potential benefits to participants or society. If there are no direct benefits, state this as well.]

    Confidentiality

    We will take steps to protect your confidentiality, including:

    • Storing data securely (e.g., password-protected files, locked cabinets).
    • Not sharing your identifying information with anyone outside the research team.
      Your data will be used only for the purposes outlined in this consent form. [State whether data will be shared, anonymized, or destroyed after the study.]

    Compensation

    [If applicable, explain any compensation, incentives, or reimbursements. If none, state: “You will not receive any compensation for your participation.”]

    Contact Information

    If you have questions or concerns about this study, you may contact:

    • Principal Investigator: [Name and Contact Information]
    • Institutional Review Board (IRB): [Insert contact for reporting concerns, if applicable.]

    Consent Statement

    By signing below, you acknowledge that you have read this form (or it has been read to you), you understand the information, and you voluntarily agree to participate in this study. You will receive a copy of this form for your records.

    Test

    Consent from

    "*" indicates required fields

    By signing this document with an electronic signature, I agreee that such signature will be as valid as handwritten signatures to the extent allowed by local law.
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    You are Taking Great Strides!

    30 Day

    Cold Plunge to Reduce Anxiety Protocol

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