The Short Consent Form For Research is a critical document required for any research involving human participants in Canada. It serves as the primary tool for documenting informed consent in accordance with the Tri-Council Policy Statement (TCPS 2) and provincial research ethics guidelines. This document should be used whenever conducting research with human participants, whether in academic, clinical, or commercial settings. It must include clear information about the study's purpose, procedures, risks, benefits, and participant rights while maintaining simplicity and accessibility. The form ensures compliance with Canadian research ethics requirements while protecting both participant rights and researcher interests. It's particularly important as it creates a documented trail of informed consent and helps establish the ethical and legal foundation for research activities.
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1. Study Title and Research Team Information: Clear identification of the study and contact information for researchers, supervisors, and research ethics board
2. Introduction: Brief overview of the research study and purpose of the consent form
3. Purpose of the Research: Clear, concise explanation of why the research is being conducted
4. Study Procedures: What participants will be asked to do, including time commitment and location
5. Risks and Benefits: Clear description of potential risks and benefits of participation
6. Voluntary Participation: Statement that participation is voluntary and can be withdrawn at any time
7. Confidentiality: How participant information will be protected and stored
8. Compensation: Details of any payment or compensation for participation
9. Participant Rights: Overview of participant rights including withdrawal and access to results
10. Consent Declaration: Formal statement of consent with signature lines for participant and researcher
1. Audio/Video Recording Consent: Required when research involves recording of participants
2. Future Use of Data: Needed when data might be used for future research projects
3. Commercial Applications: Required when research might lead to commercial products
4. Cultural Considerations: Needed for research involving specific cultural groups or Indigenous communities
5. Biological Samples: Required when collecting biological specimens
6. Third Party Access: Needed when other researchers or organizations might access the data
7. International Data Transfer: Required when data will be transferred across borders
1. Appendix A: Detailed Study Procedures: Step-by-step description of research procedures
2. Appendix B: Privacy Information Sheet: Detailed information about data protection and privacy measures
3. Appendix C: Withdrawal Form: Form for participants to indicate withdrawal from the study
4. Appendix D: Resource List: List of support services or resources for participants
5. Appendix E: Glossary: Definitions of technical terms used in the consent form
Authors
Relevant legal definitions
Clauses
Relevant Industries
Healthcare and Medical Research
Academic Research
Pharmaceutical
Biotechnology
Psychology and Behavioral Sciences
Social Sciences
Education
Market Research
Clinical Trials
Public Health
Environmental Research
Technology and Human-Computer Interaction
Relevant Teams
Research and Development
Clinical Operations
Legal Affairs
Regulatory Compliance
Ethics Review
Data Protection
Academic Affairs
Clinical Research
Research Administration
Quality Assurance
Human Subject Protection
Research Governance
Relevant Roles
Research Director
Principal Investigator
Research Coordinator
Ethics Officer
Clinical Trial Manager
Research Ethics Board Administrator
Research Compliance Officer
Research Assistant
Study Nurse
Research Ethics Consultant
Legal Counsel
Data Protection Officer
Research Program Manager
Graduate Student Researcher
Research Department Head
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