Patient Engagement
Beyond Eligibility. Activating Real Participation.

Clinical trial recruitment today identifies who qualifies biologically — but fails to account for whether a person is able, willing, or prepared to participate. Gryt bridges that gap.

Key Takeaway

CTPA augments diagnosis-based eligibility with lived-experience intelligence — to activate, and sustain real clinical trial participation.

Over the past decade, Gryt's innovative CTPA solution has successfully enrolled high-priority trials and helped clients achieve FDA goals.

The Problem

Eligibility Criteria Miss the Full Picture

Static inclusion and exclusion criteria identify who qualifies biologically — but ignore whether a patient is able, willing, or prepared to participate. This diagnosis-only approach drives costly enrollment delays, protocol amendments, and early dropouts.

Traditional Approach

Clinical Eligibility

Diagnosis, biomarkers, and clinical attributes determine who qualifies biologically for a trial.

Critical Gap

What's Missing

Real-World Participation

Lived experience, behavioral readiness, and life circumstances determine who actually enrolls and stays.

The result: Many eligible patients do not enroll, disengage early, or drop out — especially in precision medicine, rare disease, and underrepresented populations.
Our Solution

Clinical Trial Patient Activation (CTPA)

Gryt's proven model augments traditional eligibility criteria with lived-experience and behavioral readiness factors — moving from identification to activation.

Diagnosis-Only Model

Who qualifies biologically?

  • Focuses on diagnosis, biomarkers, and clinical attributes
  • Static inclusion and exclusion criteria only
  • Does not account for lived experience or readiness
  • High rates of non-enrollment, early disengagement, and dropout
  • Costly recruitment delays and protocol amendments

Gryt's CTPA Model

Who will enroll, engage, and complete?

  • Augments clinical criteria with lived-experience intelligence
  • Identifies behavioral readiness and participation barriers
  • Surfaces actionable interventions to increase activation
  • Improves retention across the full trial lifecycle
  • Especially effective for precision medicine, rare disease, and hard-to-reach populations
🎯

Outcome

By integrating lived-experience intelligence with clinical eligibility, CTPA enables participation-ready recruitment — reducing enrollment delays, improving retention, and increasing trial success.

10+

Years Activating Patients

SCOPE Award Winner

FDA

Goals Achieved for Clients

Track Record

A Decade of Proven Results

After working with Lilly COI and leading LIVESTRONG's Clinical Trial Matching Service, David Craig co-founded Gryt Health in 2016 to close the gap between eligibility and real participation.

2016

Gryt Health Founded

Co-founded by David Craig following experience at Lilly COI and leading LIVESTRONG's Clinical Trial Matching Service.

2017

First Client: Ignyta — NTRK Trial

Gryt's first client engagement successfully supported enrollment of Ignyta's landmark NTRK clinical trial.

2019

SCOPE Participant Engagement Award

Recognized at SCOPE 2019 for industry-leading work in patient engagement and clinical trial participation.

2021

SCOPE Award — Second Recognition

Awarded again at SCOPE 2021, cementing Gryt's reputation as a leader in participant-centered trial engagement.

Now

Expanding CTPA Across Precision Medicine

Gryt continues to advance lived-experience intelligence as a core driver of clinical trial success across rare disease, oncology, and underrepresented populations.

Work With Us

Ready to Activate Your Trial?

Let's talk about how Gryt's CTPA model can reduce enrollment delays, improve retention, and help your trial succeed — especially for hard-to-reach populations.

Clinical Trial Patient Activation (CTPA)

GRYT’s “CTPA” is a proven solution to drive recruitment and support representation on high-priority clinical trials. 

We developed our innovative approach through successful collaboration with sponsors to:

  1. Position clinical trials with clearly articulated differentiators

  2. Increase awarenesss with physicians and patients based on targeted geo and demographic factors – particularly for underrepresented patients

  3. Utilize a scalable approach with real-time engagement and conversion analytics

  4. Demonstrate results and optimize efforts with bi-weekly reporting

Over the past decade, Gryt’s innovative CTPA solution has successfully enrolled high-priority trials and helped our clients achieve FDA goals.

After working with Lilly COI and leading LIVESTRONG’S Clinical Trial Matching Service, David Craig co-founded Gryt Health in 2016.

  • Gryt’s first client was Ignyta, where we helped successfully enroll its NTRK trial

  • Gryt was awarded the Participant Engagement Award at SCOPE in 2019 and 2021

Engagement by Site Location

Each pin represents a person searching on Google, saw the campaign, utilized Gryt’s engagement platform and then took action for enrollment.

Outcomes Achieved

  • Facilitated patient-focused trial education, boosting awareness and screening

  • Engaged underrepresented patients by race, ethnicity & rural settings

  • Delivered actionable insights/ analytics for overall and site-specific recruitment

  • Increased patient diversity in screening

  • KPI’s are utilized to complete the read-out for FDA Diversity Action Plan

Map of the United States showing locations of cancer care centers marked with large blue 'H' icons, hospitals, and red circles indicating 200-mile radii around sites. Locations include Nebraska Cancer Center of Western Michigan, Missouri Oncology Hematology Associates, TN Baptist Cancer Center Memphis Thoracic, LA Our Lady of the Lake Cancer Institute, Northeast Georgia Medical Center, and NJ Astera Cancer Care. Multiple smaller red markers denote other facilities across the country.