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 COMFORT administrator before the account is activated.

Request consortium access

Do you have an account? Click here to sign in

What data lives in the UDP

This prototype contains synthetic study records for demonstration. Clinical site data and external medical records will be connected in a later step.

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.

Study statistics

Participant and sample collection counts grouped by clinical site and study cohort.

Reports

Aggregate CSV exports for participant and sample collection counts.

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 participant and collection counts.
• 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 the COMFORT administrator.
• Check your approval status after signing in.

This is a prototype with working account access and synthetic demonstration data. No real patient data is involved.