Important Information
Informed Consent for Participation in Research Study
Study Title: [Insert Study Title]
Principal Investigator(s): [Name(s) and Contact Information]
Sponsor/Funding Source (if applicable): [Insert Sponsor Name]
Study Location: [Insert Study Location]
Purpose of the Study
The purpose of this study is to [briefly explain the purpose in simple terms]. We aim to [state goals/objectives of the research].
Procedures
If you agree to participate, you will be asked to:
- [Describe activity, e.g., complete a survey, attend an interview, use an app, etc.]
- [Include time commitment, e.g., sessions lasting 30 minutes each for 3 weeks].
- [Mention data collection methods, e.g., audio recordings, questionnaires, biological samples].
Participation is voluntary, and you may withdraw at any time without penalty.
Risks and Benefits
Potential Risks:
- [List any risks or discomforts, including emotional, physical, or privacy-related risks.]
Potential Benefits:
- [Describe benefits to participants or broader societal benefits.]
Confidentiality
Your information will be kept confidential. Only authorized members of the research team will have access to your data. [Describe measures to protect data, e.g., secure storage, anonymization].
If findings are published, no personally identifying information will be included.
Voluntary Participation
Your participation is completely voluntary. You may choose not to participate or withdraw from the study at any time without any consequences.
Compensation (if applicable)
[Explain any compensation, reimbursement, or incentives for participation.]
Questions or Concerns
If you have any questions about this study, you can contact [Principal Investigator] at [email address/phone number]. For questions about your rights as a participant, you may contact [Institutional Review Board contact information, if applicable].