SubjectWell, the global patient experience platform for clinical trials, announced a major advancement this week. They unveiled a new SubjectWell science-driven framework. This integrated, evidence-based approach is designed to guide and transform the entire clinical trial recruitment and engagement lifecycle. The framework incorporates three key data sets:
- Patient Burden Index (PBI)
- Site Burden Index (SBI)
- Standards-of-care data
Transforming the Trial Lifecycle
Consequently, this integration allows trial sponsors to have unprecedented visibility into a study’s true operational impact. This visibility extends to participants, investigators, and recruitment teams before enrollment even begins. Fred Martin, CEO of SubjectWell, stated, “We are pioneering the next era of evidence-based recruitment by integrating burden indices and standard-of-care benchmarks directly into the core planning processes.”
Therefore, the framework delivers benefits across all phases of the trial:
- Protocol Review & Feasibility: PBI and SBI are used to evaluate how factors like visit schedules and eligibility criteria affect real-world participation. This highlights feasibility risks early on.
- Recruitment Modeling: Burden indices are merged with historical data to create science-grounded feasibility predictions. This ensures recruitment strategies precisely match the study’s operational complexity.
- Engagement and Retention: Accurate knowledge of patient burden enables SubjectWell to personalize communication and develop compassionate strategies for patient engagement. Care-against benchmarks assist in recognizing situations where patients may drop-off, thereby providing the opportunity for pre-emptive support to ensure that patients stay committed.
Additionally, sponsors obtain more accurate feasibility assessments, predictable funnel modeling, and enhanced patient and site experiences. To sum up, SubjectWell’s revamped SubjectWell science-driven framework is leading to the establishment of a new industry standard for scientific, transparent, and human-centered clinical trial processes worldwide.
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News Source: PRNewswire.com
