The Short Consent Form For Research is a critical document used in Australian research settings to obtain informed consent from study participants. It is designed to comply with the National Statement on Ethical Conduct in Human Research, the Privacy Act 1988, and relevant state/territory legislation. This document is required whenever human subjects are involved in research projects, whether in academic, medical, or commercial settings. The form must be approved by an appropriate Human Research Ethics Committee (HREC) before use and should be accompanied by a detailed participant information sheet. It includes essential information about the research project, potential risks and benefits, privacy protections, and participant rights, while maintaining clarity and accessibility for diverse participant groups.
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1. Project Title and Investigator Details: Clear identification of the research project and contact details of the research team
2. Invitation Statement: Brief, welcoming statement inviting participation in the research study
3. Project Overview: Clear, simple explanation of the research purpose and what participation involves
4. Time Commitment: Expected duration of participation and frequency of any required activities
5. Participant Requirements: Clear description of what participants will need to do
6. Risks and Benefits: Clear statement of potential risks and benefits of participation
7. Privacy and Confidentiality: Explanation of how personal information will be protected and data stored
8. Voluntary Participation: Statement that participation is voluntary and can be withdrawn at any time
9. Consent Declaration: Formal statement of consent with signature block and date
1. Compensation: Details of any payment or reimbursement offered, included when participants will receive payment or compensation
2. Future Use of Data: Information about potential future use of research data, included when data may be used beyond the current project
3. Commercial Interests: Declaration of any commercial interests or potential commercialization, included when research has commercial aspects
4. Cultural Considerations: Specific cultural considerations or protocols, included when research involves specific cultural groups
5. Translation Statement: Statement about availability of translated materials, included when participants may not be fluent in English
6. Audio/Visual Recording Consent: Specific consent for recording, included when research involves audio or visual recording
7. Genetic Testing Information: Specific information about genetic testing and implications, included for genetic research
1. Research Procedures Detail: Detailed description of specific research procedures or tests
2. Participant Information Sheet: Detailed information about the research study that participants can keep
3. Withdrawal Form: Optional form for participants to formally withdraw from the study
4. Emergency Contact Information: Form for emergency contact details if required by the nature of the research
5. Rights and Responsibilities Summary: Summary of participant rights and responsibilities in bullet point format
Relevant legal definitions
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Healthcare
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Scientific Research
Pharmaceutical
Medical Devices
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Psychology
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Market Research
Clinical Trials
Public Health
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Relevant Teams
Research & Development
Legal
Compliance
Ethics
Clinical Operations
Data Protection
Quality Assurance
Regulatory Affairs
Human Resources
Project Management Office
Relevant Roles
Research Director
Principal Investigator
Research Coordinator
Ethics Committee Officer
Clinical Trial Manager
Research Assistant
Data Protection Officer
Legal Counsel
Compliance Manager
Research Ethics Administrator
Quality Assurance Manager
Research Program Manager
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