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KHR Assent Child Version 1.219.02.19IRAS 238319ASSENT FORM CHILD 015 KHR ID Number: KHR Title of Project: United Kingdom Histiocytosis Registry (KHR)To be completed by the child in the presence of
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Begin by reading the consent form thoroughly to understand the purpose, procedures, risks, and benefits of the research.
02
If you have any questions or concerns, consult with the researcher or study team before proceeding.
03
Fill out the personal information section accurately, providing your name, contact details, and any other necessary demographics.
04
Review the sections describing the research study in detail, including the objectives, methods, and duration.
05
Ensure you understand any potential risks or discomforts involved in participating in the research.
06
Evaluate the benefits and potential outcomes of the research study.
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If you agree to participate, sign and date the consent form.
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Keep a copy of the signed consent form for your records.
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Remember, you have the right to withdraw your consent at any time during the research study.

Who needs consent for research into?

01
Anyone who wishes to participate in a research study needs to provide consent.
02
Consent is required for adults who have the capacity to understand the research study and make informed decisions.
03
For minors or individuals who may have limited capacity to consent, a parent or legal guardian usually provides consent on their behalf.
04
In some cases, additional consent may be required from individuals such as healthcare providers or institutional representatives.
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Consent for research is obtained from individuals to ensure that they understand and agree to participate in a research study.
Researchers conducting the study are required to obtain and file consent from participants.
Consent forms for research should be filled out with clear and easy-to-understand language, outlining the purpose of the study, risks involved, and the rights of the participant.
The purpose of consent for research is to protect the rights and welfare of research participants by ensuring they are informed about the study and voluntarily agree to participate.
Consent forms for research should include information on the purpose of the study, risks and benefits, confidentiality, and the rights of the participant.
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