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Get the free INFORMED CONSENT DOCUMENT - hiptchiro.com

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HAWAII PHYSICAL THERAPY & CHIROPRACTIC CLINIC, INC. Marveled H. Latah Yo, D.C., R.P.T. & Banana J. Latah Yo, P.T., D.P.T. 261 Waianuenue Avenue, Hilo, Hawaii 96720 (808)9615663 Fax (808)9693767INFORMED
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How to fill out informed consent document

01
Step 1: Read the informed consent document carefully to understand the purpose, procedures, risks, and benefits of participating in the study.
02
Step 2: Provide your personal information accurately, such as your full name, date of birth, and contact details.
03
Step 3: Make sure you understand all the terms and conditions stated in the document before signing it.
04
Step 4: If you have any questions or concerns, seek clarification from the researcher or study coordinator before signing the document.
05
Step 5: If you are satisfied with the information provided and willing to participate, sign the informed consent document.
06
Step 6: Keep a copy of the signed document for your records.

Who needs informed consent document?

01
Any individual who is invited to participate in a research study or clinical trial needs an informed consent document.
02
This includes potential participants of medical studies, psychological research, social science surveys, and any other type of scientific investigation involving human subjects.
03
Minors and individuals with cognitive disabilities may require a legal guardian or representative to sign on their behalf.
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Informed consent document is a form that explains the risks, benefits, and alternatives of a medical treatment or procedure to the patient before they can make a decision.
Healthcare providers, doctors, or medical professionals are required to file informed consent documents.
The informed consent document is typically filled out by the healthcare provider or doctor and signed by both the provider and the patient.
The purpose of the informed consent document is to ensure that the patient understands the treatment or procedure they are about to undergo and consents to it.
The informed consent document must include information about the nature of the treatment or procedure, risks involved, benefits, alternatives, and any potential complications.
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