# Closing the GAPS: Guideline Adherence, Prevention and Surveillance in Hereditary Cancer

> **NCT06654466** · NA · RECRUITING · sponsor: **Nest Genomics** · enrollment: 100 (estimated)

## Conditions studied

- Hereditary Cancer Syndromes
- Clinical Decision Support

## Interventions

- **DEVICE:** Nest, an electronic medical record (EMR)-integrated software platform to deliver longitudinal, genetics-based care at scale.

## Key facts

- **NCT ID:** NCT06654466
- **Lead sponsor:** Nest Genomics
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2026-02-10
- **Primary completion:** 2027-03
- **Final completion:** 2027-09
- **Target enrollment:** 100 (ESTIMATED)
- **Last updated:** 2026-02-25

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06654466

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06654466, "Closing the GAPS: Guideline Adherence, Prevention and Surveillance in Hereditary Cancer". Retrieved via AI Analytics 2026-06-25 from https://api.ai-analytics.org/clinical/NCT06654466. Licensed CC0.

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