The Short Consent Form For Research is a fundamental document required for any research involving human participants in England and Wales. It serves as a legal record of informed consent and is designed to protect both the participants' rights and the researchers' interests. The form must comply with UK GDPR, the Data Protection Act 2018, and various research governance frameworks. It typically includes essential information about the study, data handling procedures, participant rights, and researcher responsibilities. This document is particularly crucial for ensuring ethical research conduct and maintaining regulatory compliance across academic, medical, and social research sectors.
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1. Study Title: Clear identification of the research project and version number
2. Principal Investigator Information: Name, institution, and contact details of the lead researcher and research team
3. Purpose of Research: Brief, clear explanation of research objectives in plain language
4. Participation Statement: Confirmation that participation is voluntary and can be withdrawn at any time
5. Data Protection Statement: Information about how personal data will be collected, stored, used and protected in compliance with UK GDPR
6. Signature Block: Space for participant name, signature, date, and researcher countersignature
1. Biological Samples Section: Details of sample collection, storage, and usage when research involves human tissue samples
2. Future Research Use: Optional consent for data or sample use in future research projects
3. Payment Information: Details of any compensation or reimbursement for participation
4. Audio/Video Recording: Specific consent for recording of interviews or procedures if applicable
5. Medical Records Access: Permission to access relevant medical records if required for the research
1. Participant Information Sheet: Detailed information about the study, risks, benefits, and participant rights
2. Withdrawal Form: Template form for participants to withdraw from the study
3. Contact Card: Emergency contact information for research team and relevant support services
4. Schedule of Procedures: Timeline and list of research procedures, visits, or interventions
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