Proove EverythingSomething
Launch clinical observational studies in minutes with AI-powered protocol generation. Collect real-world patient outcomes with validated PRO instruments.
How It Works
From intervention to insights in five steps
Define Intervention
Enter what you're studying. AI analyzes the clinical context.
Design Protocol
AI generates endpoints, PRO instruments, consent, and safety rules.
Enroll Participants
Share a link. Participants consent and screen on mobile.
Collect Outcomes
Validated PROs with automated reminders and safety monitoring.
Analyze Results
Real-world evidence from patient outcomes and lab data.
Five Specialized Agents
Working together to design, launch, and run your study
Protocol Agent
Designs study endpoints, inclusion/exclusion criteria, and PRO instruments.
Safety Agent
Creates intervention-specific safety rules, alert thresholds, and monitoring protocols.
Consent Agent
Generates plain-language informed consent with comprehension verification.
Enrollment Agent
Guides participants through registration, consent, and eligibility screening.
Engagement Agent
Sends personalized reminders and milestone messages to maximize retention.
TRT Outcomes Study
A telehealth company wants to measure patient outcomes for testosterone replacement therapy. This demo shows how they can launch an observational study in minutes using our AI agents.
- 26-week observational study
- qADAM, IIEF-5, PHQ-2 instruments
- Automated safety monitoring
Everything You Need to Run a Study
Validated PRO Instruments
qADAM, IIEF-5, PHQ-2, and other validated questionnaires selected for your intervention.
Auto-Generated Consent
Plain-language informed consent documents with comprehension verification.
Safety Monitoring
Automatic alerts when participants exceed safety thresholds on PROs or labs.
Smart Engagement
AI-crafted reminders and milestone messages to maximize participant retention.