Consent captures a signature. It does not create understanding.Protocols define participation. They do not prepare people for it.CORE closes the gap before confusion becomes dropout.
CORE maps every trial lifecycle stage to specific education, expectation-setting, and decision support that patients need to participate successfully.
All materials are protocol-derived, behaviorally structured, IRB-ready, consistent across sites, and amendment-resilient. CORE removes execution risk at every stage where confusion, fear, or unmet expectation derails participation.
CORE follows a structured three-phase process. Each phase answers a specific question. Each phase produces output that feeds the next. Nothing is created from assumption. Nothing is built without clarity on what it must accomplish. Full deployment happens in weeks, not months.
Traditional patient education informs. Clinical trials demand commitment. CORE bridges that gap with behavioral design: decision architecture over information delivery, sequencing over compression, expectation alignment over persuasion, feasibility framing over clinical framing, caregiver integration by default, amendment resilience over static delivery.
Patients don't struggle from lacking information. They struggle translating information into real-life feasibility. CORE sequences how decisions unfold, not how protocols are written. It helps patients answer "Can I really do this?" not just "What is this?"
Amendments are the number one reason traditional patient education fails mid-study. Generic, monolithic materials get rebuilt from scratch. Timelines reset. Patient understanding regresses. CORE's modular architecture preserves what works and updates only what changed.
Protocol change identified. Scope assessed against existing CORE materials.
Affected lifecycle stages and assets identified. Unaffected materials remain in service.
Only impacted components revised. Patient understanding already built is preserved.
In most trials, caregivers determine feasibility. They manage schedules, transportation, medication, support, and decisions. Caregiver readiness and patient readiness are inseparable. A prepared patient with an unprepared caregiver is a retention risk. CORE eliminates the gap by design.
A concrete map of time commitment, decision points, physical presence, and emotional labor. Caregivers know what they are agreeing to before the patient consents.
Protocol burden falls on caregivers differently. CORE translates requirements into caregiver-specific terms: schedule, work, travel, cognitive load.
Caregivers participate in enrollment, continuation, and withdrawal decisions. Decision support is built for the caregiver's perspective.
CORE delivers through modular assets, each grounded in insight, designed for comprehension, built for reuse and scale.
Start with one asset. Prove value quickly with live deployment. Expand across indications, trials, populations. Reuse and adapt without rebuilding.
Poor execution creates screen failure, early dropout, site burden, delays, and rescue spend. Every confusion point becomes a cost center. CORE prevents structural inefficiency by preparing patients before trials absorb the cost of confusion.
By preventing avoidable dropout and rescue, CORE materially reduces cost per completer and protects timeline integrity.
CORE delivers prepared patients to sites by establishing understanding and aligning expectations upfront, reducing rework, escalations, and coordinator burnout.
CORE turns completion from a hope into a designed outcome by making readiness an explicit, governed input to participation.
Powering 17 of the world's top 25 pharmaceutical companies.
CORE is Jumo Health's trial execution system for patient readiness education. It translates protocol design into structured, behaviorally informed education for patients, caregivers, and sites across five lifecycle stages. Protocol-derived. IRB-ready. Deployed in weeks.
Agencies are creative-led and slow. Content libraries store generic assets. CORE is execution-first, protocol-derived, and behaviorally structured. Every asset has a defined role, mapped to a specific decision point in the trial lifecycle.
CORE deploys in six to eight weeks. Pre-built behavioral formats and structured outputs eliminate long creative cycles, scope drift, and rework. Standard package first, then expansion by protocol complexity.
Yes. CORE materials are amendment-resilient. Modular assets update only the impacted components without resetting patient understanding. Turnaround in days, not weeks.
Caregivers are a readiness variable, not an audience. CORE includes role definition, burden translation, and decision partnership in every stage. Caregiver readiness and patient readiness are inseparable.
CORE is a trial execution system for patient readiness education. PRISM is a full operating system: education plus readiness intelligence, governed advancement, and retention monitoring. Deploy CORE standalone or as the foundational layer within PRISM.
Proprietary constructs defined by Jumo Health. Each one is a measurable operational concept, not a marketing term. View all definitions →
In two days, you get three execution diagnostics on your program.
How likely each eligible patient cluster is to activate, persist, and complete, before any intervention.
The barriers most likely to suppress activation, enrollment, and completion in each cluster, and how to mitigate them.
Which clusters to target, which barriers to address, which interventions to deploy, and what completion lift to expect.