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Combined Consent and Authorization to Participate in a Research Study Novel actions of to augment resistance training adaptation in older adults WHY ARE YOU BEING INVITED TO TAKE PART IN THIS RESEARCH?
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Start by reviewing the www.ahrq.gov/funding/policies/sample-combined-informed-consent document.
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Read and understand the purpose of the informed consent form.
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Make sure you have all the necessary information and documents, such as the patient's medical history and current condition.
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Begin by filling in the patient's personal details, including their name, date of birth, and contact information.
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Provide a clear explanation of the study or procedure for which the informed consent is required.
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Include all the potential risks, benefits, and alternatives associated with the study or procedure.
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Clearly state that participation is voluntary and the patient can withdraw at any time.
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Ensure that the patient understands the information provided by using simple and clear language.
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Who needs wwwahrqgovfundingpoliciessample combined informed consent?

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Anyone conducting medical research studies or procedures that require informed consent would need the www.ahrq.gov/funding/policies/sample-combined-informed-consent form. This includes healthcare professionals, clinical researchers, and institutions carrying out studies involving human subjects.
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It is a consent form that combines various funding policies and guidelines into one document.
Researchers and institutions receiving funding from AHRQ are required to file the combined informed consent.
The combined informed consent form can be filled out electronically or manually following the instructions provided by AHRQ.
The purpose is to ensure that research participants are fully informed about the risks and benefits of the study, as well as their rights and protections.
The form should include details about the study, potential risks and benefits, participant rights, and contact information for questions.
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