Workflow is usable
Referrals are appropriate, first contact is timely, barriers move toward resolution, and partner burden is acceptable.
The proposed scorecard separates activity from completion. A referral sent is not a barrier resolved. A reminder delivered is not transportation arranged. The six-month pilot should show where practical work closes, where it stalls, and where it needs escalation or redesign.
These demo charts use seeded prototype cases only. A live pilot would require partner-approved metric definitions, privacy controls, and reporting rules before any patient-level or aggregate data are shared.
Count of identified support needs across seeded and locally created demo cases.
Resolution status across all practical tasks in the Non-Clinical Recovery Support Plans.
The first pilot is meant to test the operating model, integration burden, workforce model, and practical-resolution process before making claims about clinical effectiveness.
Active caseload, overdue practical tasks, escalation volume, Navigator capacity, resource gaps, and referral issues.
Enrollment, first-contact performance, barriers by category, resolution rates, handoffs, patient experience, and workflow changes.
Formal checkpoint on eligibility, staffing, supervision, privacy boundaries, resource availability, technology, and partner burden.
Summarize feasibility, process outcomes, feedback, costs, risks, lessons learned, and the issues that must be addressed before any larger launch.
The partner and AfterNest should agree in advance on the evidence needed to continue, redesign, narrow, or stop the program.
Referrals are appropriate, first contact is timely, barriers move toward resolution, and partner burden is acceptable.
Eligibility, staffing, training, resource access, technology, or escalation needs material redesign.
The model performs better for a specific population, barrier category, or service line.
Clinical-boundary failures, low engagement, unresolved operational risk, or poor feasibility would argue against expansion.
The proposal identifies patient and healthcare worker feedback and lower post-discharge issues or complications as desired measures. This prototype directly demonstrates process measures; any claim about clinical outcomes would require an appropriate study design and partner-approved analysis.