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This document contains essential information regarding the professional services provided by Tracy Payton Watson, MA, LPC, outlining client rights, responsibilities, therapeutic processes, confidentiality, and various treatment modalities offered, including hypnotherapy and EMDR. It emphasizes the importance of informed consent in establishing a therapeutic relationship.
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How to fill out informed consent

01
Start by providing a clear title for the consent form.
02
Include the purpose of the study or procedure.
03
Describe the procedures involved and what participants will be required to do.
04
Explain any potential risks or discomforts that may arise.
05
Outline the benefits of participation for the individual or others.
06
Inform participants about their right to withdraw at any time.
07
Include confidentiality assurances regarding personal information.
08
Provide contact information for questions or concerns.
09
Ensure space for the participant’s signature and date.

Who needs informed consent?

01
All participants in clinical trials or research studies.
02
Patients undergoing medical procedures or treatments.
03
Individuals participating in surveys or interviews that collect sensitive information.
04
Participants in any study where personal data will be used.
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Informed consent is a process by which a patient or participant is fully informed about the risks, benefits, and alternatives of a treatment or research study and voluntarily agrees to proceed.
Researchers, healthcare providers, and institutions conducting clinical trials or medical procedures that involve patient participation are required to file informed consent.
To fill out informed consent, one must provide detailed information about the study or treatment, including its purpose, procedures, risks, benefits, and confidentiality, and obtain the participant's signature.
The purpose of informed consent is to ensure that participants understand what they are agreeing to, protect their rights and welfare, and uphold ethical standards in research and medical practices.
Informed consent must report information such as the nature of the research or treatment, potential risks, benefits, alternative options, confidentiality measures, and the right to withdraw at any time.
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