Interactive risk-assessment module hosted on your website
FindSM is a self-guided tool for consumers focused on underlying rare and genetic causes for health concerns to help kickstart conversations with healthcare providers
The User Experience
Users with concerns about a specific condition can engage in a programmed chat-like experience tailored in real-time to their answers. At completion, an educational summary is provided with a “risk score” and clinical information to share with their healthcare provider.
The Client Experience
Working as part of a larger educational initiative, FindSM integrates into your website to provide an engaging symptom app. De-identified non-PHI data is provided regularly for evaluation.
“The project with ThinkGenetic has sparked significant interest within our organization. As a result, we have scheduled a wider, regional roll-out across our Growth & Emerging Markets Business Unit which spans almost 50 countries. Additionally, within the wider Takeda community, our global colleagues are considering its implementation in other countries and regions.”
Marie Gray, Regional Franchise Head, Rare Metabolic Disease & Neuroscience, Takeda
1 Based on validated sensitivity and specificity of algorithms for two genetic conditions
Ready to see FindSM in action?
How to Utilize FindSM on Your Site
Develop
The ThinkGenetic genetic subject matter experts create or update an interactive self-reporting tool to uncover a user’s risk level for a rare disorder. The first steps in the process include:
- The creation, validation, and refinement of algorithms focused on signs and symptoms of a specific condition
- The creation of a printable / downloadable fact sheet with the user’s clinical signs and actionable next steps to share with a healthcare provider
Deploy
The ThinkGenetic development team embeds the validated tool on the client’s site. Our team will assist you by:
- Providing technical support to setup and integrate the API into your site
- Providing access to an interactive report portal on tool usage and de-identified data including traffic, demographics, reported symptoms, and other key reported answers
Success and Validations
Decreasing the diagnosis odyssey of patients living with Fabry disease via a patient-centered innovative web-based platform. Read more
