Participants
Start with story, receive a personal output, and decide whether anything contributes to community or research learning.
PatientStories.ai helps teams learn from health in the wild before assumptions harden into protocols, evidence plans, support programs, and research questions.
The participant conversation leads with Health Biography and Doctor Visit Reports. The client conversation leads with evidence gaps, patient-originated signals, cohort learning, and research-ready questions.
Start with story, receive a personal output, and decide whether anything contributes to community or research learning.
Receive anonymized reflections: patterns, failure points, workarounds, questions, and “people like me” lenses.
Receive aggregated insight, signal maps, structured-question candidates, evidence-gap summaries, and recommendations for deeper study.
LEAN is the operating frame for turning open narrative into useful evidence-planning signals without pretending that stories are already formal evidence.
Start with least-friction text or voice narrative intake and recent lived moments.
Use AI-assisted decomposition to identify concepts, context, burden, timeline, workarounds, questions, and candidate fields.
Compare participant-reviewed signals across cohorts, subgroups, community lenses, and emerging themes.
Turn signals into better prompts, structured survey follow-ups, evidence-gap summaries, advisory questions, and next-step research priorities.
PatientStories.ai can sit upstream of evidence planning, protocol design, Phase IV commitments, patient support, medical affairs, advocacy partnerships, and real-world research prioritization.
Identify burdens, expectations, support gaps, and practical realities that may affect endpoints, schedules, visits, retention, and adherence.
Reveal what people are actually struggling to manage: side effects, logistics, emotions, financial friction, family burden, and workarounds.
Convert patient-originated signals into better questions for RWE, Phase IV, advisory boards, medical affairs, advocacy, and community research.
The model supports open narrative intake, participant review, Me + Community lenses, public or private dashboards, signal-based deeper dives, and data-driven structured surveys that follow the signal rather than pre-empt it.
Participants begin with text or voice. They are not forced into a chronology or rigid survey sequence before the signal appears.
AI extracts themes, variables, questions, and answer-set candidates for participant review, edit, approval, deletion, or research submission.
Aggregated patterns can generate targeted structured surveys, cohort filters, dashboards, and research questions for deeper investigation.
Aggregated themes, patient language, burden maps, workarounds, and representative de-identified patterns.
Variables, answer sets, follow-up prompts, and survey modules derived from open story patterns.
Patient-centered summaries for IEP teams, protocol design, medical affairs, Phase IV planning, and support-program strategy.
Filters and dashboards that show subgroup experience without exposing individual narratives.
Participant-informed feedback on burdens, logistics, comprehension, recruitment expectations, and operational friction.
When appropriate, the architecture can support governed observational research, IRB oversight, and defined analytic plans.
PatientStories.ai separates raw user narrative, user-reviewed semantic structure, personal Health Biography outputs, anonymized community reflection, and client-facing research insight.
The model is designed to preserve participant trust while making lived-experience signals useful to teams that plan evidence, design studies, support patients, and ask better research questions.
The participant-facing promise remains personal value first. Client outputs are aggregated, governed, anonymized, and consent-aware.
Use this path for research insight, sponsor partnerships, advocacy collaborations, LEAN signal generation, Integrated Evidence Plan support, or feasibility feedback.