Short Consent Form For Research Template for Denmark

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Short Consent Form For Research

Document background

The Short Consent Form For Research is an essential document required by Danish law for any research involving human participants. It is used to obtain and document informed consent in compliance with the Danish Act on Research Ethics Review, the General Data Protection Regulation (GDPR), and the Danish Data Protection Act. This document must be provided to potential research participants before their enrollment in any study, whether clinical, behavioral, or social science research. The form includes mandatory information about the study's purpose, procedures, risks, benefits, data handling practices, and participant rights. It serves as both a legal record of consent and an educational tool to ensure participants understand what their participation entails. The document must be written in clear, accessible language while meeting all regulatory requirements of Danish research ethics committees and data protection authorities.

Suggested Sections

1. Study Information: Title of the research study, principal investigator's name and contact information, and sponsoring institution

2. Purpose of Research: Brief, clear explanation of the research purpose in lay terms

3. Participation Requirements: What the participant will be asked to do and the time commitment required

4. Risks and Benefits: Clear statement of potential risks and benefits of participation

5. Voluntary Participation: Statement that participation is voluntary and can be withdrawn at any time

6. Data Protection: How personal data will be collected, used, stored, and protected in compliance with GDPR

7. Contact Information: Contact details for questions about the research and participant rights

8. Consent Declaration: The actual consent statement and space for participant signature

Optional Sections

1. Compensation: Include when participants will receive payment or reimbursement for participation

2. Future Research Use: Include when data or samples might be used for future research projects

3. Commercial Development: Include when research might lead to commercial products

4. Audio/Video Recording: Include when the research involves recording of participants

5. Biological Samples: Include when the research involves collection of biological samples

Suggested Schedules

1. Detailed Study Protocol Summary: Brief summary of the full research protocol in lay language

2. Rights as a Research Participant: Detailed explanation of participant rights under Danish law and GDPR

3. Emergency Contact Information: List of emergency contacts and procedures (required for medical research)

4. Data Processing Information: Detailed information about data processing activities and data protection measures

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