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! Jason Northrup, Ph.D., LEFT, LPC INSTITUTE FOR COUPLE AND FAMILY ENHANCEMENT ! THERAPY INFORMATION AND CONSENT TO TREATMENT The purpose of this document is to ensure that all participants in the
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How to fill out informed consent 2015 update:

01
Start by reviewing the informed consent form carefully. Pay attention to any changes or updates that have been made from previous versions.
02
Verify that all required information is present on the form. This typically includes the name and contact information of the participant, the purpose of the study or procedure, the risks and benefits involved, and any alternatives available.
03
Ensure that the consent form includes a clear explanation of the participant's rights and the voluntary nature of their participation. It should also outline the confidentiality measures that will be taken to protect their personal information.
04
Make sure that the participant has sufficient time to review the consent form and ask any questions they may have. Provide them with additional resources or explanations if needed.
05
If any changes are made to the consent form during the process of obtaining informed consent, document these changes properly and ensure that the participant is informed about them.
06
Obtain the participant's signature or, in some cases, their legally authorized representative's signature, on the consent form. This signifies their understanding and agreement to participate.
07
Keep a copy of the signed consent form in the participant's records and provide them with a copy for their own reference.

Who needs informed consent 2015 update?

01
Researchers conducting studies involving human participants are required to obtain informed consent. This includes both academic and industry-sponsored research.
02
Healthcare professionals who perform medical procedures or treatments that carry certain risks to the patient must obtain informed consent before proceeding.
03
Informed consent is also necessary for any situation where an individual may be subject to potential harm or the disclosure of personally identifiable information, such as for certain clinical trials or data collection activities.
Please note that the specifics of informed consent requirements may vary depending on the jurisdiction and the nature of the study or procedure. It is important to consult relevant laws, regulations, and ethical guidelines to ensure compliance.

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