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Appendix I Informed Consent Title of Study: Thriving despite adversity: Ugandan community nurses experiences Background and Purpose of study: You have been invited to participate in a study whose
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Appendix I informed consent is a form that provides documented proof of an individual's voluntary agreement to participate in a specific study or medical procedure, fully understanding the potential risks and benefits associated with it.
Both the researcher or medical professional conducting the study or procedure and the participant or their legal representative are required to file appendix I informed consent.
To fill out appendix I informed consent, the participant or legal representative must read the document carefully, ask any questions they may have, and then sign and date it to acknowledge their voluntary participation.
The purpose of appendix I informed consent is to ensure that individuals are well-informed about the details and potential risks and benefits of a study or medical procedure before they decide to participate, thereby protecting their rights and welfare.
Appendix I informed consent should include information about the nature and purpose of the study or procedure, any potential risks and benefits, alternatives available, confidentiality measures, and contact details of the researcher or medical professional.
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