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����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����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
Relevant legal definitions
Clauses
Relevant Industries
Healthcare
Academic Research
Clinical Trials
Social Sciences
Psychology
Educational Research
Public Health
Medical Technology
Pharmaceutical
Biotechnology
Health Services Research
Population Studies
Behavioral Sciences
Relevant Teams
Research & Development
Clinical Operations
Legal & Compliance
Regulatory Affairs
Ethics & Governance
Data Protection
Clinical Research
Academic Research
Research Administration
Quality Assurance
Cultural Advisory
Patient Safety
Relevant Roles
Research Director
Principal Investigator
Research Coordinator
Clinical Trial Manager
Ethics Committee Member
Research Ethics Officer
Legal Counsel
Privacy Officer
Research Administrator
Research Nurse
Study Coordinator
Research Compliance Officer
Cultural Advisor
Regulatory Affairs Manager
Data Protection Officer
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