Help Center

Guides for site coordinators & staff

You run the study day to day at your site: you add and enroll participants, collect consent, enter visit data, record adverse events and medications, and answer queries.

Getting started

Account & sign-in

eConsent

Participants

Data entry

Safety reporting

Queries, review & locks

Randomization & supplies

Trial management

Emails, texts & reminders

Troubleshooting

Guides for other roles

Still need help?

Email support@capture.study or use the contact form. Tell us the study name, what you were trying to do and the exact message on screen; a screenshot helps.

Please never send participant names, contact details or health information to support.