What informed consent actually is
Informed consent is an ongoing conversation, not a single signature. It is the process of learning what a study involves so you can decide freely whether to take part.
Know what you sign. Keep your choice.
Joining is always voluntary. You can leave at any time.
Five ideas every volunteer should know
Voluntary participation
No one should pressure you to decide on the spot.
Understanding study risks
Potential benefits, described honestly
Some studies offer no direct personal benefit. A good consent form says so clearly and explains how the research may help others in the future.
Benefits are possible, never promised.
Confidentiality and your information
Types of studies
Consent looks different in every study.
the big picture
General Clinical Research
A broad term for studies that involve people and aim to answer health-related questions.
watch and record
Observational Studies
Researchers observe and record information without assigning a specific intervention.
something is tested
Interventional Studies
Volunteers are assigned to receive a specific intervention so researchers can study its effects.
habits and choices
Behavioral Studies
Studies that look at habits, choices, or programs such as sleep, exercise, or learning routines.
How it works
Three steps. No pressure.
- 01
Read
Short guides to each part of a consent form.
- 02
Ask
Bring our question list to the study team.
- 03
Decide
Sign only when you feel ready. Or say no.
Walk in prepared.
Ask a question, or choose optional texts. Account notifications and Marketing messages, only if you check them.
Informed Research Guide is an independent consent guide website. It is not a research organization, study sponsor, or healthcare provider, and it does not conduct research, enroll participants, or provide health advice.