One place for all Project-COMFORT study data

Project-COMFORT explores patient-centric microsampling (PCmS) as a gentler alternative to conventional venous blood draws. The Unified Digital Platform (UDP) brings the anonymised study data together — participants, visits, blood sample collections, safety records and questionnaire feedback — so the consortium and the wider community can follow the study with confidence.

Sign up as a visitor

A standard sign up, activated straight away. You get access to the Statistics and Reports pages with aggregated, anonymised results only.

Create a visitor account

Sign up as a consortium user

Full access to the participant index, study visits, collections and safety data. Requests are reviewed and approved by the Consortium admins before the account is activated.

Request consortium access

Do you have an account? Click here to sign in

What data lives in the UDP

Study information is synchronised from the clinical sites and stored in an anonymised, unified repository. No directly identifying patient data is held in the platform.

Participant index

Anonymised participant records, cohorts, consent status and enrolment in Part A and Part B.

Study visits

Screening and follow-up visits per participant, with date, part, place, status and comments.

Blood sample collections

Venous and capillary collections, microsampling devices, kit codes, volumes and analyte results.

Safety and adverse events

Adverse event records with short-term effects, probable cause and action taken.

Statistics and endpoints

Aggregated KPIs, protocol endpoints for Part A and Part B, and usability questionnaire results.

Reports

Ready-made exports covering participants, visits, collections, safety and legal information.

Who can access the platform

Access is granted at two levels, so aggregated findings stay open while participant-level data stays protected.

Visitors

Instant access

• Anyone can register with a standard sign up form.
• Access to the Statistics page with study KPIs and endpoints.
• Access to the Reports page with aggregated exports.
• No access to the participant index or individual records.

Consortium users

Approval needed

• For partners, investigators and site staff working on the study.
• Full access to participants, visits, collections and adverse events.
• Each request is reviewed and approved by a Consortium admin.
• You are notified by email once your account is activated.

This is a demo environment for showcasing the platform. No real authentication or patient data is involved.