Collaborative Approach to Reach Everyone With Familial Hypercholesterolemia (CARE-FH)
At a glance
Conditions
NCT05284513
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Geisinger Clinic
Multiple Locations, Pennsylvaniano site contact published
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Laney K Jones, PharmD, MPH · PRINCIPAL_INVESTIGATOR · Geisinger Clinic
- Samuel S Gidding, MD · PRINCIPAL_INVESTIGATOR · Geisinger Clinic
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
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Inclusion
Exclusion
What this trial measures
- FH diagnosis rate (Aim 2)Up to 45 months
FH diagnosis rate, is achieving both the scheduling of a clinic visit and evidence the clinician, at that visit, has completed evidence-based FH diagnostic evaluation, defined as completing one of: using the FH clinic note to document care, adding FH diagnosis on the problem list, using the FH smart-set (or ordered a genetic test for FH), making a referral to the lipid clinic, or starting a statin for an evidence-based indication
- Acceptability (Aim 3)Month 9, 12, 18, 24, 30, 36, 42
Clinician and patient satisfaction and self-efficacy with the FH diagnosis program
- Timeliness (Aim 4)Up to 45 months
Time to FH screen, time to diagnostic evaluation, time to statin initiation