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Participant Information and Consent Form (Adolescents) Title: Effects of exercise intensity in obese children and adolescents Principal Investigator: Miss Katrin Dias Supervisor: Professor Jeff Comes
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How to fill out participant information and consent

01
Start by gathering all the necessary information about the participant, including their name, address, contact details, and any relevant identification numbers.
02
Create a participant information form that includes fields for each piece of required information. Ensure that the form is clear and easy to understand.
03
Provide clear instructions on how to properly fill out the participant information form. Include any specific guidelines or requirements.
04
Ensure that the participant understands the purpose and use of their information, as well as any potential risks or benefits associated with providing their consent.
05
Obtain the participant's consent to collect and use their information by having them sign a consent form. The consent form should clearly explain the purpose and scope of data collection, how the information will be stored and protected, and any rights the participant has regarding their data.
06
Review the filled-out participant information form and consent form for accuracy and completeness. Make sure all required fields are filled in properly.
07
Securely store the participant's information and consent forms in compliance with any applicable data protection regulations.
08
Regularly review and update participant information as necessary, ensuring that the collected data remains accurate and up to date.
09
Inform the participant of any changes in the way their information will be used or stored, and obtain their updated consent if necessary.

Who needs participant information and consent?

01
Any organization or individual conducting research, surveys, or studies that involve collecting personal data of participants needs participant information and consent.
02
This includes academic researchers, healthcare providers, market research firms, and any other entity that requires participant data for their activities.
03
Participants' information and consent are necessary to ensure compliance with ethical standards and legal regulations regarding data privacy and protection.
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Participant information and consent is a document that outlines the details of an individual participating in a study or research project, including their personal information and their agreement to participate.
Researchers or organizers of a study are required to file participant information and consent.
Participant information and consent forms are typically filled out by providing the necessary personal details of the participant and obtaining their signature to indicate their agreement to participate.
The purpose of participant information and consent is to ensure that individuals are fully informed about a study or research project before agreeing to participate, and to document their voluntary consent.
Participant information and consent forms typically include personal details such as name, contact information, age, and any relevant medical history, as well as a description of the study and its potential risks and benefits.
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