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Participant Information Sheet/Consent Form Nonintervention Study Adult providing own consent Repatriation General Hospital Title Investigating gait and balance in Cervical Dystonia Coordinating Principal
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How to fill out a participant information sheet/consent form:

01
Start by reading the instructions provided on the form carefully. It will outline what information is necessary and how to accurately fill out the form.
02
Begin by providing your personal information such as your name, contact details, and any other information specifically requested. This is important for identification purposes.
03
Next, ensure that you understand the purpose of the form and what it is being used for. This will help you provide accurate and relevant information.
04
Fill out any medical information that may be required, such as allergies or existing medical conditions. It is crucial to disclose any conditions that may affect your participation in the specific activity or research project.
05
If applicable, provide emergency contact details. This is important in case of any unforeseen circumstances or emergencies that may arise during participation.
06
Read and understand the consent section of the form. This section typically outlines the purpose of the study or activity, any potential risks involved, and your rights as a participant. Make sure you are comfortable with the terms and give your informed consent by signing and dating the form.
07
Review the form for accuracy and completeness before submitting it. Double-check all the information you have provided to ensure it is correct and that you have not missed any required fields.
08
Keep a copy of the filled-out form for your records. This can be useful in case there are any questions or issues that arise in the future.

Who needs a participant information sheet/consent form:

01
Researchers conducting studies or experiments that involve human participants typically require participants to fill out a participant information sheet/consent form. This is to ensure that participants are fully informed about the study, its purpose, and any potential risks involved before giving their consent to participate.
02
Organizations or institutions hosting events or activities that require participant information or consent may also use these forms. This can include fitness classes, workshops, or other similar events where personal information and consent are necessary for participation.
03
Medical practitioners or healthcare providers may require patients to fill out participant information sheets/consent forms for specific treatments or procedures. This is to ensure that patients are fully informed about the treatment, its potential risks, and give their consent before proceeding.
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The participant information sheet/consent form is a document that provides all the necessary information about a study to a potential participant, and also obtains the participant's consent to take part in the research.
Researchers conducting a study involving human subjects are required to provide and file a participant information sheet/consent form.
The form should be filled out by the researcher with all relevant study details, risks and benefits, confidentiality agreements, and the participant's consent language.
The purpose of the form is to ensure that participants have all the necessary information to make an informed decision about participating in a study, and to obtain their voluntary consent.
The form must include study details, risks and benefits, confidentiality agreements, contact information for the researcher, and consent language.
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