What You Need to Know to Participate
This document provides information to help you decide whether to join this research study. It is important you understand the responsibilities, risks and benefits of participating.
Informed Consent Form
Study Title: The Effects of Digital Wellness Apps on Daily Stress Levels
Principal Investigator: Dr. Jane Smith
Institution: Center for Digital Health Research
Contact Information: jsmith@cdhr.org | (123) 456-7890
Introduction
You are being asked to participate in a research study. Participation is voluntary. This form explains the purpose of the study, what you will be asked to do, any risks and benefits, and your rights as a participant. Please read this form carefully and ask any questions before deciding whether to take part.
Purpose of the Study
The purpose of this study is to evaluate the impact of using a digital wellness app on reducing self-reported stress in adults over a 30-day period.
What You Will Be Asked to Do
If you agree to participate, you will:
- Complete a brief online survey at the beginning and end of the 30-day period.
- Use a digital wellness app for at least 5 minutes per day for 30 days.
- Answer weekly check-in questions about your mood and stress levels.
Estimated time commitment: Approximately 2 hours total over the 30-day period.
Risks and Discomforts
- Some questions may be personal or cause minor emotional discomfort.
- There are no known major risks associated with participation.
Benefits
- You may gain insights into your own stress patterns.
- Your participation may help improve digital wellness tools for others.
Note: You will not be paid for participating in this study.
Confidentiality
All data will be stored securely and only accessible to the research team. Responses will be de-identified before analysis. We will not share your personal information with third parties.
Voluntary Participation and Withdrawal
Your participation is entirely voluntary. You may withdraw at any time without penalty. If you choose to withdraw, any data collected up to that point may still be used unless you request otherwise.
Questions
If you have any questions about the study, you may contact the principal investigator using the information above. If you have questions about your rights as a research participant, contact the Institutional Review Board at (123) 555-0000 or irb@cdhr.org.
Consent
By signing below, you acknowledge that:
- You have read and understood the information above.
- You have had the opportunity to ask questions.
- You voluntarily agree to participate in this study.
Participant Name (Printed): ___________________________
Signature: _________________________________________
Date: ___________________
Researcher Name (Printed): ___________________________
Signature: _________________________________________
Date: ___________________