Clinical research, made clear.
Plain words. Five simple steps. No pressure.
Study types
Five kinds of research
General Clinical Trials
Organized studies that look at how a new approach works for people. Volunteers follow a written plan called a protocol.
Health Research
A broad field that studies how the body works, how conditions develop, and how care can improve over time.
Behavioral Research
Studies about habits, routines, sleep, stress, or learning. Many involve surveys, interviews, or simple activities.
Observational Studies
Researchers watch and record what happens naturally. Volunteers are not asked to change anything about their care.
Interventional Studies
Volunteers try a specific approach, such as a new routine or product, so researchers can compare results.
Features
Made for beginners
- Beginner-friendly articles
- Clinical research facts
- Public research links
- Introductory guides
- Awareness newsletter
How it works
From curious to confident
STEP 01
Learn the basics
Read about how studies work and what different study types involve.
STEP 02
Explore public listings
Browse public study directories to see what kinds of studies exist near you.
STEP 03
Contact the study team
Each independent study team explains its own requirements and answers questions.
STEP 04
Review the consent document
Take your time, ask questions, and talk with your own healthcare provider.
STEP 05
Decide what is right for you
Joining is always your choice, and you can change your mind.
FAQ
Common questions
What is clinical research?
Clinical research is any study that involves people and aims to answer a health question. It helps researchers learn what works, what does not, and for whom.
What is a protocol?
A protocol is the written plan for a study. It explains who can join, what happens at each visit, and how long the study lasts.
What are study phases?
Many trials move through phases. Early phases involve a small group and focus on safety. Later phases include more people and compare approaches.
Who reviews a study?
In the United States, studies involving people are usually reviewed by an Institutional Review Board, a group that checks that the plan protects volunteers.
What is informed consent?
Before joining, volunteers receive a document explaining the study, its possible risks, and their rights. Signing it is a choice, and volunteers can leave a study at any time.
Ready to learn the basics?
Optional texts. Free to read. Your choice.
Everyday Research Awareness