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Affirming Alternatives Psychological Services, P.C. Dr. Kathleen Young, Pay. D., Licensed Clinical Psychologist 1348 West Glen lake Avenue Chicago, Illinois 60660 7733811922 Informed Consent for Participation
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How to Fill Out Informed Consent - Kathleen:

01
Begin by reading the informed consent form carefully. Make sure to fully understand the purpose, risks, benefits, and alternatives associated with the study or procedure.
02
Fill in your personal information accurately, including your full name, date of birth, contact details, and any other required details.
03
Review the nature of the study or procedure outlined in the form. It is crucial to comprehend what you are consenting to, so don't hesitate to seek clarification from the healthcare professional or researcher if you have any doubts or questions.
04
Sign and date the informed consent form. By doing so, you are stating that you have understood the information provided and have voluntarily agreed to participate or undergo the procedure.
05
If the study or procedure involves risks or potential side effects, make sure to acknowledge your understanding and acceptance of these risks by initialing or signing the relevant sections of the form.
06
Keep a copy of the signed informed consent form for your records. It's important to have a personal copy as a reference and to ensure that you are aware of what you have consented to.

Who Needs Informed Consent - Kathleen:

01
Informed consent is typically required for any medical or research-related study involving human participants. This includes clinical trials, medical procedures, psychological studies, and other forms of human subjects research.
02
Kathleen, or any individual participating in a medical study or procedure, would need to provide informed consent. This ensures that they have a clear understanding of the study or procedure, its associated risks and benefits, and voluntarily agree to participate.
03
Informed consent is also necessary for vulnerable populations, such as minors, individuals with cognitive impairments, or those unable to give consent themselves. In such cases, a legally authorized representative may provide consent on behalf of the individual.
Remember, it is essential to consult with the healthcare provider, researcher, or Institutional Review Board (IRB) for specific guidelines and requirements regarding informed consent in your particular situation.
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Informed consent refers to the process of obtaining permission from a patient before conducting a medical procedure or treatment, ensuring the patient understands the risks and benefits involved.
Healthcare providers, researchers, and medical professionals are required to obtain and file informed consent from patients before proceeding with any treatment or study.
To fill out informed consent, the healthcare provider must clearly explain the procedure or treatment, discuss potential risks and benefits, answer any questions the patient may have, and have the patient sign the consent form.
The purpose of informed consent is to ensure that patients are fully informed about the medical procedures or treatments they are about to undergo, allowing them to make educated decisions about their healthcare.
Informed consent forms typically include details about the procedure or treatment, potential risks and benefits, alternative options, and the patient's right to refuse or withdraw consent.
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