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Department of Kinesiology 9201 University City Blvd Charlotte, NC 28223 Informed Assent / Consent for Charlotte Ankle Sprain Tracking Study (CASTS) Project Title and Purpose You are invited to participate
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How to fill out informed assent consent form:

01
Start by reading the entire form carefully. Make sure you fully understand the purpose and scope of the consent.
02
Provide your personal information accurately, including your name, age, and contact details.
03
Understand the study or procedure being conducted and its potential risks and benefits. If you have any questions, don't hesitate to ask the researcher or person in charge.
04
Informed assent consent forms usually require you or your guardian to initial or sign specific sections to indicate your understanding and agreement. Follow the instructions and complete these sections accordingly.
05
If there are any additional documents or attachments that need to be included with the form, ensure you have them before submitting.
06
Carefully review the completed form once again to ensure all sections are filled out accurately and completely.
07
If you are of legal age, sign and date the form. If you are a minor, both you and your parent or guardian will need to sign and date the form.
08
Return the completed form to the appropriate person or institution as instructed.

Who needs informed assent consent:

01
Minors: Informed assent consent is usually required for minors who are not legally able to provide their own informed consent. It ensures that they understand the study or procedure and agree to participate in a way that is appropriate for their age and understanding.
02
Individuals with cognitive impairments: Informed assent consent may also be required for individuals with cognitive impairments who may not have full capacity to provide informed consent. This ensures that they understand the study or procedure to the best of their ability and are willing to participate.
03
Certain research studies or medical procedures may also require informed assent consent from adults, particularly when they involve sensitive topics or potential risks.
Overall, the informed assent consent form is a crucial document in research or medical settings to ensure that individuals, particularly minors and those with cognitive impairments, understand the details of a study or procedure and willingly agree to participate.
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Informed assent consent is for obtaining agreement from individuals who may not have the legal capacity to give consent themselves, such as minors or those with cognitive impairments.
Researchers and healthcare providers are typically required to file informed assent consent for participants who are unable to give full consent.
Informed assent consent forms should be filled out with clear and simple language, ensuring that all risks and benefits are clearly explained to the participant.
The purpose of informed assent consent is to ensure that participants who cannot give full consent are still able to provide some level of agreement to participate in research or medical treatment.
Informed assent consent forms should include details about the research or treatment, potential risks and benefits, and any alternative options available to the participant.
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