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PARTICIPANT INFORMATION SHEET: CONSENT FOR COLLECTION OF OUTCOME DATA TITLE:Effect of breathing support during delayed cord clamping (DCC) for very preterm infants. Short title:The ABC study Assisted
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How to fill out participant information sheet consent

01
To fill out the participant information sheet consent, follow these steps:
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Start by reading the consent form carefully to understand the information and requirements.
03
Provide your personal details such as your name, age, contact information, and any other requested information.
04
Make sure to review and understand the purpose of the study or research, as well as the potential risks and benefits involved.
05
If you have any questions or concerns, don't hesitate to seek clarification from the researcher or study team.
06
Sign and date the consent form to indicate your voluntary agreement to participate.
07
Keep a copy of the consent form for your reference.
08
If there are any updates or changes to the study, ensure that you are provided with updated consent information and have the opportunity to review and provide consent again if necessary.
09
Note: It's important to remember that providing informed consent is a personal decision, and you should feel comfortable and well-informed before agreeing to participate.

Who needs participant information sheet consent?

01
Anyone who will participate in a study or research project that requires their personal information and involvement needs a participant information sheet consent.
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This includes participants of clinical trials, surveys, interviews, focus groups, or any other type of research study where consent is necessary to ensure the voluntary and informed participation of individuals.
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Participant information sheet consent is a document that outlines the details of a study, including the risks and benefits of participation, and is signed by the participant to indicate their understanding and agreement to take part in the study.
Researchers conducting a study are required to provide a participant information sheet consent to all individuals being invited to participate in the study.
Participant information sheet consent should be filled out by providing all necessary study details, including the purpose of the study, potential risks and benefits, confidentiality measures, and contact information for questions or concerns.
The purpose of participant information sheet consent is to ensure that participants are fully informed about the study they are being asked to participate in, and to obtain their voluntary agreement to take part.
Participant information sheet consent must include details about the study purpose, procedures, risks, benefits, confidentiality, voluntary participation, and contact information for questions or concerns.
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