The Short Consent Form For Research is a crucial document in New Zealand's research landscape, designed to facilitate ethical research while protecting participant rights. It is required whenever research involves human participants, whether in clinical, academic, or social science settings. The document must comply with the Health Research Council guidelines, Privacy Act 2020, and other relevant New Zealand legislation. This form serves as both a legal record of consent and an informational tool, ensuring participants understand their involvement, rights, and the study's implications. It includes provisions for data protection, cultural sensitivity (especially regarding M锟斤拷锟斤拷ori participants), and clear withdrawal procedures. The form must be approved by an ethics committee before use and is typically accompanied by a more detailed participant information sheet.
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1. Title and Header Information: Research study title, institution details, and reference numbers
2. Researcher Information: Names and contact details of principal investigator and research team
3. Study Purpose: Brief, clear explanation of the research purpose and objectives
4. Participation Details: What participation involves, including time commitment and procedures
5. Risks and Benefits: Clear statement of potential risks and benefits of participation
6. Data Privacy and Confidentiality: How personal information will be collected, stored, and protected
7. Participant Rights: Right to withdraw, access information, and ask questions
8. Consent Declaration: Explicit statements of what the participant is consenting to
9. Signatures: Spaces for participant and researcher signatures, dates
1. Cultural Considerations: Section addressing specific cultural aspects, particularly for M锟斤拷锟斤拷ori participants, following Te Ara Tika guidelines
2. Future Research Use: Optional consent for use of data in future research projects
3. Audio/Video Recording Consent: Specific consent for recording of interviews or procedures, if applicable
4. Compensation Information: Details about any compensation or reimbursement for participation
5. Translation Statement: For forms translated from English, certification of translation accuracy
6. Witness Statement: Where a witness is required for vulnerable participants or those unable to read/write
7. Medical Disclosure: For health-related research, permission to access medical records or contact healthcare providers
1. Participant Information Sheet: Detailed information about the study that participants can keep
2. Contact Information Sheet: List of relevant contacts including ethics committee, support services
3. Study Procedures Schedule: If applicable, timeline of study visits or procedures
4. Withdrawal Form: Optional form for participants to formally withdraw from the study
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