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INFORMATION FOR CLIENTS Psychotherapy Practice Information Brochure Christy Duffy, PhD, HSP Clinical Psychologist Director, Under the Umbrella, LLC 1136 W. 17th St., Suite B Bloomington, IN 47404 (812)

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How to fill out informed consent - under

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Step 1: Explain the purpose of the study to the participants.

02

Step 2: Clearly state the risks and benefits of participating in the study.

03

Step 3: Provide a detailed explanation of the procedures involved and the time commitment required.

04

Step 4: Inform participants of their rights, including the right to withdraw from the study at any time.

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Step 5: Obtain the participant's signature on the consent form to indicate their voluntary participation in the study.

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Step 6: Make sure the participant receives a copy of the signed consent form.

Who needs informed consent - under?

01

Informed consent is required for any research or medical study involving human participants.

02

This includes clinical trials, surveys, interviews, experiments, and other forms of data collection.

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Both adults and minors (with parental or guardian consent) may need to provide informed consent depending on the nature of the study.

04

Informed consent ensures that participants understand the purpose, risks, and benefits of the study before agreeing to participate.

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What is informed consent - under?

Informed consent is a process for getting permission before conducting a healthcare intervention on a person.

Who is required to file informed consent - under?

Healthcare providers are required to ensure that informed consent is obtained from patients before performing any medical procedure or treatment.

How to fill out informed consent - under?

Informed consent forms should be filled out by providing all relevant information about the proposed treatment, risks, benefits, and alternatives to the patient.

What is the purpose of informed consent - under?

The purpose of informed consent is to respect the autonomy of patients and ensure they have a full understanding of the medical intervention they are about to undergo.

What information must be reported on informed consent - under?

Informed consent forms should include details about the procedure, risks involved, benefits of the treatment, alternative options, and the patient's right to refuse treatment.

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