Hope for HIE – Hypoxic Ischemic Encephalopathy Hope for HIE – Hypoxic Ischemic Encephalopathy

Research & Consulting

THE GLOBAL PULSE ON HIE - ACCELERATING RESEARCH & DEVELOPMENT

Hope for HIE's leadership and global community have decades of expertise in best practice development for patient advocacy involvement in clinical trials - from the TOBY and Shankaran trials to the completion of the HEAL study, and everything in between and in the future.

We are experts in patient-family communication and engagement, navigating patient-family focused regulatory requirements and insights, and regularly consult and collaborate on various stages of research and development for scientific and therapeutic areas relating to HIE, on both the academic and industry/drug and device development sides.

  • Patient-family insights in therapeutic & MedTech development
  • Facilitation and access with key opinion leaders
  • Clinical trial design
  • Patient-Family Centered core outcome setting and measurement
  • Patient educational material design & development
  • Patient-family engagement and communication strategy
  • IRB-approved focus group and survey methodology
  • Regulatory compliance support
  • Longitudinal partnership and support for research/product development
  • Comprehensive Halo of Support©️ clinical trial model & framework
  • Development & facilitation of patient-family advisory councils
  • Clinical trial design
  • Core outcome setting and measurement
  • End-to-end patient-family engagement and communication strategy management for optimal data capture
  • IRB-approved consent, focus group and survey methodology
  • Study dissemination design and strategy
  • Regulatory and commercialization support
Partnership Statement

At Hope for HIE, our partnerships in research are grounded in integrity, authenticity, and accountability to the families we serve.

We do not participate in “checkmark engagement,” nor do we accept the “wink-wink, nudge-nudge” tokenism that too often characterizes stakeholder involvement in research. Our community deserves better—and we expect better from anyone who seeks to work alongside us.

For more than a decade, Hope for HIE has championed family-integrated care, patient-centered research, and respectful, reciprocal collaboration. When we partner in research, it is because the work has meaningful potential to advance science, improve care, and reflect the lived experience of those most impacted by HIE. We bring forward the needs, priorities, and diverse voices of our global community, and we do so with transparency, rigor, and a commitment to long-term relationship-building.

Families are not a box to check. Their perspectives are not an optional add-on. Their trust is not something to be leveraged for funding or optics.

Their expertise is essential—and we protect it fiercely.

We will continue to engage only in research partnerships where we and our families are respected as true collaborators, the value of our collective experience is honored, and the work aligns with our mission to improve outcomes, strengthen care, and accelerate discovery across HIE.

Contact Us

Participating in Clinical Trials

We've put together a comprehensive hub for HIE families interested in learning more about clinical trials and research studies with some of the best resources to help build health literacy, understand how clinical trials and research studies for hypoxic ischemic encephalopathy and associated diagnoses work, and links to active and upcoming trials of interest to families.

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