Clinical Trial Recruiting
Accelerate clinical trial recruitment today
Transform clinical trial recruiting by engaging directly with qualified participants based on patient-consented real-world data.
Human API is a patient engagement platform that connects and converts health data from multiple sources — transforming data into intelligence.
Identify eligible, motivated participants and reach out to them directly for clinical trial opportunities.
Precise matching
Match eligible patients to trials using Real-World Data (RWD) like electronic health records, and refine matches by condition, procedure, medication, demographics, location, and more.
Direct engagement
Engage directly with motivated patients who have expressed interest in being contacted about research opportunities.
Faster enrollment
Improve site confidence in referrals by streamlining consent and sharing collected health information, ultimately accelerating trial eligibility determination to enroll sooner.
A traditional approach to clinical trial recruiting is no longer sufficient.
Many life sciences organizations rely on service providers and physicians to recruit patients. Some organizations are in the early stages of leveraging technology to identify ideal clinical research sites and physicians for clinical trials, based on patient population. This inherently limits reach to patients and relies on third-parties to engage with them.
For example, the National Cancer Institute conducted a trends study earlier this year, revealing that only 9% of people surveyed have ever been invited to participate in a trial. Despite all the options available, recruiting still consumes a significant amount of time and budget for clinical trials.
How it works
1. Identify qualified participants
Leverage your patient registry and Human API’s captive database of users to identify patients that may qualify for a trial based on demographics, location, clinical observations (diagnosis, medications, test results, etc), survey results, and more.
2. Engage with participants
Define cohorts based on queries of real-world data (RWD) and generate lists of eligible participants for follow-up outreach. Trigger outreach to those patients in the form of configurable emails and SMS texts.
3. Track success of screening and enrollment
Track activity throughout the participant journey — including email engagement, task engagement and completion rates, and rates of data retrieval. Easily refer participants and share their data with sites.
Other Use Cases
Patient Registries
Streamline patient engagement and acquire health data — from any source, at any time.
Patient Services
Perform timely, personalized outreach for support programs and digital companion applications
