Article

Using the CFIR 2.0 Framework to Assess the Implementation of GARDE: A Population Health Management Tool for Hereditary Cancer Risk

2026-07-30

Abstract excerpt

<title>Abstract</title> <p> <bold>Background:</bold> Identifying individuals at increased hereditary cancer risk remains challenging in primary care settings due to limited time with providers, low self‑efficacy in family history collection, and evolving referral guidelines. Genetic Cancer Risk Detector (GARDE), a population‑level open-source software platform, uses electronic health record (EHR)-based family h...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 83a4b864-df10-5e51-bdc5-ddb359d15165
DOI: 10.21203/rs.3.rs-10070047/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Using the CFIR 2.0 Framework to Assess the Implementation of GARDE: A Population Health Management Tool for Hereditary Cancer RiskDOI 10.21203/rs.3.rs-10070047/v1Read

Lessons learned from the pilot phase of a population wide genomic screening program: Building the base to reach a diverse cohort of 100,000 participantsSemantic proximity Read

Implementation Mapping for Managing Patients at High Risk for Hereditary Cancer.Semantic proximity Read

Adaptation and pilot implementation of a hereditary cancer risk-assessment tool for primary care.Semantic proximity Read

What it Takes to Implement Population-Based Genomic Screening: A Multi-Site Qualitative Study of Implementation Determinants Across Health SystemsSemantic proximity Read

Streamlining Inherited Cancer Identification via an EMR-Integrated Risk Assessment Platform: A Nonrandomized Clinical Trial.Semantic proximity Read

Strategies to Assess Risk for Hereditary Cancer in Primary Care Clinics: A Cluster Randomized Clinical Trial.Semantic proximity Read

Pragmatic implementation research study for In Our DNA SC: a protocol to identify multi-level factors that support the implementation, adaptation, and sustainment of a population-wide genomic screening initiative in diverse populationsSemantic proximity Read

Family history and cancer risk study (FOREST): A clinical trial assessing electronic patient-directed family history input for identifying patients at risk of hereditary cancer.Semantic proximity Read

The implementation of large-scale genomic screening or diagnostic programmes: A rapid evidence reviewSemantic proximity Read

Implementing Primary Care Mediated Population Genetic Screening within an Integrated Health SystemSemantic proximity Read

Patient and primary care provider experience using a family health history collection, risk stratification, and clinical decision support tool: a type 2 hybrid controlled implementation-effectiveness trial.Semantic proximity Read

IMProving care After inherited Cancer Testing (IMPACT) study: protocol of a randomized trial evaluating the efficacy of two interventions designed to improve cancer risk management and family communication of genetic test results.Semantic proximity Read