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RED#: 15538 STUDY INFORMATION AND CONSENT FORM TITLE OF STUDY: Dynamic Noise Reduction in Accelerometer based Mechanomyography during Pediatric Gait INVESTIGATORS: Tom Chat, PhD, (Engineer×, Researcher,
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Start by carefully reading through the study information and consent form. Make sure you understand the purpose of the study, the procedures involved, and any potential risks or benefits.
02
Provide your personal information accurately. This may include your name, contact details, age, gender, and any relevant medical history. Ensure that all the information is up-to-date and correct.
03
Read the consent section thoroughly. This section should outline your rights as a participant, including the option to withdraw from the study at any time. If you have any questions or concerns about the consent form, don't hesitate to seek clarification from the study coordinator or researcher.
04
If you agree to participate in the study, sign the consent form. Your signature signifies that you have understood the information provided and willingly consent to being part of the study.
05
Keep a copy of the study information and consent form for your records. It's important to have a copy for future reference and in case you need to refer back to any details throughout the study.

Who needs study information and consent:

01
Individuals who are being recruited to participate in a specific research study.
02
Any person who has been approached by a researcher or study coordinator with the aim of involving them in a study.
03
Participants who want to understand the purpose, procedures, and potential risks or benefits associated with the study before giving their informed consent.
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Study information and consent is a document that provides details about a research study to participants, including the purpose of the study, potential risks and benefits, and the rights of participants.
Researchers conducting a research study are required to file study information and consent with the appropriate regulatory bodies.
Study information and consent forms are typically filled out by researchers and reviewed by an ethics committee before being given to study participants.
The purpose of study information and consent is to ensure that participants are fully informed about a research study before deciding whether or not to participate.
Study information and consent forms must include details about the study purpose, procedures, risks and benefits, confidentiality, and the rights of participants.
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