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Consent/Assent for Participation in a Research Project (For people with diagnosed T2DM) Explanatory Statement Study Title: Community based lifestyle intervention for diabetes management in Nepal:
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Read the consentassent form carefully to understand the purpose and requirements of the participation.
02
Provide all the requested personal information accurately in the designated fields.
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Ensure that you have understood the terms and conditions of the participation and agree to them.
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If you have any questions or concerns, contact the responsible person or organization for clarification.
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Sign the consentassent form using your legal name and date it.
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Submit the completed form to the appropriate person or organization as instructed.

Who needs consentassent for participation in?

01
Anyone who is planning to participate in a specific activity, research study, event, or program that requires consent or assent may need consentassent for participation.
02
Minors or individuals who are incapable of providing informed consent themselves may require consentassent from their legal guardians or representatives.
03
Participants in medical trials, psychological research studies, educational programs, or any other activities that involve potential risks or legal responsibilities usually need to fill out a consentassent form.
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Consentassent ensures that participants understand the nature of the activity, potential risks or benefits, and their rights and responsibilities before agreeing to participate.
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Consent and assent for participation refer to the process of obtaining permission from individuals (or their guardians) to take part in a study, including research involving human subjects.
Researchers conducting studies involving human participants are required to obtain and file consent or assent from participants or their legal representatives.
To fill out consent or assent forms, ensure that all required information is provided, including the purpose of the study, procedures involved, potential risks, and the rights of participants. Signatures from participants or their guardians are also necessary.
The purpose of consent and assent is to protect the rights and welfare of research participants by ensuring they are informed about the study and voluntarily agree to participate.
The consent/assent form must include details about the study's purpose, procedures, risks, benefits, confidentiality, the right to withdraw, and contact information for questions.
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