The Short Consent Form For Research is a fundamental document required for conducting research involving human subjects in Qatar. This document is essential for ensuring ethical research practices and protecting participants' rights while complying with Qatar's regulatory framework, including Law No. 2 of 1983 and the Qatar Supreme Council of Health Guidelines. The form must be used before commencing any research involving human subjects, whether in medical, academic, or social science contexts. It provides participants with clear, concise information about the study, their rights, and the handling of their personal data, while meeting both local and international ethical standards. The document's format balances the need for comprehensive information with accessibility, ensuring participants can make informed decisions about their participation.

1. Research Project Title and Introduction: Clear identification of the research project and brief introduction to the study purpose

2. Researcher Information: Names and contact details of principal investigator and research team

3. Purpose of the Study: Brief, clear explanation of research objectives in lay terms

4. Participation Requirements: What participants will be asked to do, including time commitment and procedures

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

6. Confidentiality and Data Protection: How participant information will be protected and used, aligned with Qatar's data protection laws

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 Voluntary Participation: Statement that participation is voluntary and can be withdrawn at any time

8. Contact Information: Details for questions or concerns, including ethics committee contact

9. Declaration of Consent: Formal consent statement and signature section