The Dissertation Consent Form is a critical document required by Saudi Arabian academic institutions for all research involving human participants. This document must be obtained before conducting any dissertation research and serves multiple purposes: it ensures compliance with Saudi Arabian research ethics guidelines, protects participants' rights, and documents informed consent. The form must be completed in accordance with the Saudi Law of Universities and National Committee of Bioethics (NCBE) Guidelines. It typically includes detailed information about the research project, data collection methods, confidentiality measures, and participant rights. The Dissertation Consent Form may need to be provided in both Arabic and English, depending on the participant population, and must be approved by the institution's ethics committee before use.
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1. Parties: Identification of the student researcher, academic institution, and research supervisor(s)
2. Background: Brief context of the research project and purpose of the consent form
3. Definitions: Key terms used in the consent form including 'Research', 'Data', 'Dissertation', 'Confidential Information'
4. Purpose of Research: Detailed description of research objectives and methodology
5. Participant Rights: Clear outline of participant's rights, including right to withdraw
6. Data Collection and Usage: Details of what data will be collected and how it will be used
7. Confidentiality Measures: Description of how confidentiality will be maintained
8. Declaration of Consent: Formal consent statement and signature blocks
1. Audio/Video Recording Consent: Additional consent section when interviews or sessions need to be recorded
2. Translation Declaration: Required when the research involves non-Arabic speaking participants
3. Parent/Guardian Consent: Required when research participants are minors or vulnerable adults
4. Compensation Details: Required when participants will receive payment or compensation
5. Medical Disclaimer: Required for research involving health-related data or medical information
1. Research Project Summary: Detailed overview of the research project methodology and objectives
2. Data Protection Protocol: Detailed procedures for data handling and protection
3. Interview Questions: List of proposed interview questions or research instruments
4. Risk Assessment: Evaluation of potential risks to participants and mitigation measures
5. Withdrawal Form: Template form for participants to withdraw from the research
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