A consent-aware screening funnel for studies where vascular cognition matters.
VascuMind helps identify, educate, baseline, and route people with vascular cognitive concerns before a sponsor spends deeply on downstream screening.
Research teams need better-fit candidates before expensive screening steps.
High screen-fail waste
Sponsors can spend heavily on biomarker confirmation before cognitive and vascular fit are clear.
Weak vascular differentiation
Many recruitment funnels do not separate ischemic-pattern, mixed, and non-vascular cognitive concerns early enough.
Poor consumer trust
Listing sites rarely create the plain-language confidence families need before they opt into research follow-up.
Consumer-grade front door. Vascular differentiation. Structured memory baseline. Consent-aware routing.
Find subtle cognitive impairment and vascular-risk context before late-stage disease.
Route ischemic-pattern and mixed impairment into better-aligned trial pathways.
Use one funnel for recruitment, baseline characterization, and repeat testing.
Flexible, value-aligned licensing tailored to study scope.
We structure licensing around study complexity, volume, and the level of implementation support needed. Specific pricing is discussed deal-by-deal after understanding your indication, sites, cohort size, and analytics requirements. Our benchmark: parity or premium to legacy cognitive tools when paired with vascular differentiation, ischemic-pattern fit, and campaign analytics.
Pilot
Single-study feasibility, one indication, defined site cohort
Standard
Active trial program with recruitment, screening, and monitoring workflow
Enterprise
Multi-study, multi-region, or trial-network deployment
Why custom pricing?
- Study scope varies: single indication vs. multi-study programs, regional vs. global
- Implementation depth: self-serve configuration vs. full managed deployment
- Analytics needs: basic conversion tracking vs. source-level cohort analytics
- Volume commitments: pilot feasibility vs. guaranteed enrollment targets
- All discussions include: implementation timeline, support SLA, and renewal terms
- Stroke/TIA history questions
- Blood-flow and vascular risk prompts
- Clinician conversation checklist
Implementation workflow
- Define indication, inclusion/exclusion logic, countries, sites, participant volume, and consent requirements.
- Configure a condition-specific landing page, ischemic pattern check, memory baseline handoff, and research-interest form.
- Launch source-tracked campaigns and monitor conversion by message, site, audience, and score band.
- Use structured exports and operating reviews to refine recruitment, prequalification, and follow-up.
Compliance posture
- Educational and trial-screening positioning, not consumer diagnosis.
- Clinical validation claims must be sourced and reviewed before sponsor materials.
- Consent, privacy, site requirements, and country-specific rules must be defined before deployment.
- No identifiable consumer data is shared with sponsors or CROs without additional explicit consent.
Give sponsors a consumer-grade trial-readiness engine.
The DTC funnel creates awareness. The CRO license monetizes validated demand where vascular cognition matters most.
Preview Licensing One-Pager