SBIR/STTR Research Award

Leveraging Large Language Models to Enhance Regional Genomic Medicine eConsults

Award identifier 90c8e487a136ebaf3f04a23e91680c81c6b8d6fc84dbe06c78e6650409215ee8Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$400,618

Program and phase

SBIR · Phase I

Award year

2025

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
CARE PROGRESS LLC
Proposal award date
2025-09-20
Contract end date
2026-08-31
UEI
G1NZTU5F4FQ8
Solicitation number
PAR24-106
Topic code
172

Research abstract

Project Summary/Abstract Primary care physicians (PCPs) have limited genetics knowledge, including knowing if and when to order genetic/genomic testing and which tests to order. While genetics and other specialty societies have created robust clinical practice guidelines to define the appropriate genetic evaluation for defined indications, they are typically complex and PCPs lack sufficient time or expertise to assess the need for genetics consultation or testing for a specific patient. Further, given the ever-increasing and evolving medical knowledge base, PCPs lack time to stay current with guideline updates. As a result, PCPs may make clinical decisions that are not fully informed and result in substandard care, with potentially suboptimal clinical outcomes. To address these issues, we propose to leverage large language models (LLM) to create an AI assistant tool to help PCPs and clinical genetics professionals enhance guideline-concordant genetic eConsultations. Our approach is superior to creating clinical decision support rules, which have not been robust and must be manually updated whenever guidelines change. Aim 1 focuses on developing methods to combine large language models with clinical practice genetics guidelines for quality, semi-automated eConsult recommendations. In doing so, we will develop extensible methods for digitizing guidelines so that LLMs can access them to determine if a given patient meets criteria for ordering a specific test, whether a genetics consultation is warranted and other tasks. Our second aim is to demonstrate the usability of a prototype among PCPs. Using user-centered design principles, we will build a Web-based Chatbot prototype of our innovation. We will then recruit PCPs and perform usability reviews, including administering a usability questionnaire. We will also obtain qualitative feedback from PCPs. If we are successful, we will demonstrate the feasibility of our tool to enable PCPs to make informed clinical decisions at the point of care, including ordering genetic testing, which will enhance eConsultations with clinical genetics professionals, including reducing the time a patient has to wait for consultation and treatment, and ultimately improving clinical outcomes.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

10 SBIR/STTR records share this UEI (2014–2025). Reported award amounts total $6,324,466. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services, National Science Foundation

Agency intelligence

Department of Health and Human Services

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