Research & innovation

Evidence that improves care—fast.

Evermore research focuses on real-world outcomes: safer pathways, better follow-up, and smarter patient experiences. We validate interventions, measure impact, and translate findings into everyday care.

Explore outputs Partner with us

Governance-first

Ethics + safety baked in

Outcome-led

Measure what matters

Patient-centric

Clear consent and control

Research snapshot

What we publish & measure

A balanced mix of pragmatic trials, pathway reviews, safety audits, and guidelines—focused on real patient outcomes.

Pragmatic trials

Real-world effectiveness and adherence

Clinical audits

Safety signals + measurable improvements

Guidelines

Protocol clarity and repeatable outcomes

Datasets

De-identified metrics for benchmarking

Want to run a study with us?

Share your hypothesis, proposed cohort, and desired outcomes. We’ll respond with governance and feasibility steps.

Collaborate

Built for reliability, privacy, and clinical safety

Governance-ledAudit-readyDe-identified metricsSecure workflows

Focus areas

What we research

Clinical research that’s practical, measurable, and designed to improve patient outcomes without adding friction.

Browse outputs

Cardiology & Prevention

Risk stratification, early detection, and patient-centred prevention pathways.

Hypertension pathways

Arrhythmia monitoring

Preventive screening

Collaborate

Imaging & Diagnostics

Faster diagnosis with careful validation and safety-first governance.

Radiology workflows

Clinical decision support

Accuracy audits

Collaborate

Dermatology

Earlier triage and consistent outcomes through evidence-backed protocols.

Inflammatory skin disease

Lesion triage

Follow-up outcomes

Collaborate

Orthopaedics

Rehab optimisation, pain pathways, and post-procedure monitoring.

MSK triage

Recovery tracking

Outcome measurements

Collaborate

Digital Health

Evidence for portal features, remote monitoring, and patient engagement.

Portal usability

Remote check-ins

Adherence support

Collaborate

Safety & Quality

Audit-led improvements, incident reduction, and clear accountability.

Clinical audits

Safety signals

Continuous improvement

Collaborate

How we run research

A governance-first process

Clear checkpoints so studies move fast while staying safe: define, validate, review, run, publish, improve.

1) Define the question
Outcome-first: what changes for the patient if this works?
2) Minimise risk & data
Minimum necessary data, clear consent, and safety-by-design.
3) Governance review
Ethics, privacy, feasibility, and clinical owner sign-off.
4) Run & monitor
Recruitment rules, safety signals, and continuous monitoring.
5) Analyse & publish
Transparent reporting with clear limitations and next steps.
6) Translate into care
Turn findings into pathways, training, and measurable improvements.

Ethics & privacy

Patient control, always

Clear consent, minimum necessary data, and safeguards for sensitive health information.

Explicit consent where required

Audit logs & accountability

De-identification for metrics

Secure access controls

Translational impact

Research that changes practice

We prioritise work that becomes safer pathways, better follow-up, fewer delays, and clearer patient experiences.

See outputs

Explore

Publications, trials, guidelines & datasets

Search outputs by topic, area, and type. These items are UI placeholders—wire them to your DB when ready.

Search & filters

Search

Type

Area

Tag

Tip: use search to find more tags.

Results

6

Matched outputs

Collaborate

Partner with Evermore Research

Universities, clinical partners, and industry teams can propose research, audits, or digital health studies. Start with a short brief.

What we like to see

Clear outcomes & feasibility

The best proposals define a measurable outcome, explain the cohort, and state what changes for the patient if the work succeeds.

A short hypothesis

Proposed cohort + timeframe

Primary outcome metric

Governance considerations

Response time

1–3 days

Typical initial reply (project dependent)

Collaboration request

Send a short brief

This is UI-only right now. If you want, I’ll wire it to a backend route (e.g. POST /api/research/collaborate) and store in Mongo + admin inbox.

FAQ

Common questions

Quick clarity on participation, ethics, privacy, and collaboration.

Research & participation

Transparent, voluntary, safe

Research participation is always opt-in, with clear information and the ability to withdraw where applicable.

You can ask questions before consenting

Participation is voluntary

Governance oversight for safety

Minimal data collection where possible