Clinical-grade participant outcomes

Capture what matters most — the patient voice

ProNova52 is a modern platform for collecting participant-reported outcomes. Design studies with 44+ question types, invite participants, and analyse results — all in one place.

Mobile
Tablet
Desktop
GDPR Compliant
AES-256 Encrypted
Clinical Governance Ready
Multi-Tenant Architecture
UK Data Residency

Built for clinical research teams

Whether you're running a small pilot or a multi-site RCT, ProNova52 adapts to your workflow.

NHS Trusts

Clinician-led PROMs collection with governance, consent, and audit trail built in.

Academic Research

University research teams use ProNova52 for longitudinal cohort studies and RCTs.

CROs & Pharma

Scalable multi-site data collection with role-based access and API integration.

Patient Charities

Patient registries and lived-experience surveys with accessible, mobile-first design.

How it works

Three steps to better outcomes data.

1

Design your study

Create your study with branding, consent flows, governance details, and a rich set of question types. Preview on mobile, tablet, and desktop before going live.

2

Invite participants

Import participants from CSV, add manually, or share a public join link. Send branded email invitations with secure invite codes and QR codes.

3

Analyse results

View real-time dashboards with completion rates, scores, and response breakdowns. Export raw data as CSV for further analysis in R, SPSS, or Excel.

Are you a study participant?

If you've received an invite code from your clinician, you can start your study right here.

Ready to modernise your research?

Join clinical teams already using ProNova52 to capture participant-reported outcomes with confidence.