CClinicalTrials.gg
Enrolling by invitationNCT05284513CARE-FHUpdated Dec 22, 2025

Collaborative Approach to Reach Everyone With Familial Hypercholesterolemia (CARE-FH)

An interventional study of FH diagnosis program and Implementation strategy package: Develop and implement tools for quality monitoring in Familial Hypercholesterolemia, sponsored by Geisinger Clinic. Enrolling by invitation at 1 site in United States. Open to participants aged 26 Years and older. Per ClinicalTrials.gov, last updated 2025-12-22.

Sponsored by Geisinger Clinic · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
532
Allocation
Randomized
Ages
26 Years and older
Sex
All
01

Study summary

Diagnosis rates of familial hypercholesterolemia (FH) are low in the United States, despite multiple guidelines and recommendations for screening and treatment of high cholesterol, to prevent heart attacks in those affected. Using a stepped-wedge design, the investigators plan to utilize tools from implementation science to improve uptake, acceptability, and sustainability of FH diagnostic programs in primary care settings. If successful, this study will provide tools generalizable to other health care systems to improve FH diagnosis rates.

Read the detailed description

Familial hypercholesterolemia (FH) is a common genetic disorder (prevalence 1 in 250) that requires lifelong sustained medical care. Evidence-based guidelines for screening and treatment for FH exist. These include universal screening of children ages 9-11, of adolescents ages 18-20, and of adults ages 40 and above; approved diagnostic tools including lipid panels and genetic testing; and recommendations for initiation of lipid lowering medication. FH diagnosis is currently made too late in life, often after a premature heart attack has occurred creating a care gap that results in excess cardiovascular morbidity and mortality. Diagnosing FH in the primary care setting would optimize treatment for individuals with FH and close this care gap. Utilizing tools from implementation science and human centered design, and by considering uptake, acceptability, and sustainability of programs related to FH care should improve earlier diagnosis. Implementation strategies that include insights from patients, clinicians, and healthcare systems are necessary. The long-term goal is to create an effective FH diagnosis program that is practical and sustainable in the real-world setting. The main objective of this project is to determine the uptake of an FH diagnosis program integrated into primary care practices to promote early identification of adult and pediatric patients that is generalizable to other healthcare settings. The research question is, does using a multi-level implementation strategy package, designed to address the specific needs of patients, clinicians, and healthcare systems, improve the diagnosis and activation of care management for individuals with FH. The specific aims are to: 1) to design a clinical trial to assess multi-level implementation strategies for improving FH diagnosis in an integrated health system, 2) compare FH diagnosis rates among primary care clinicians who receive the implementation strategy package versus those who do not, 3) to measure implementation success of an organized FH diagnosis program, and 4) to explore patient-related service and health outcomes related to an FH diagnosis program.

02

Conditions studied

  • Familial Hypercholesterolemia
03

In context

Hyperlipoproteinemia Type II

245 studies on the registry are indexed under Hyperlipoproteinemia Type II; 52 are open to participants now.

This study's planned enrollment of 532 is above the median of 86 across 170 interventional studies indexed under Hyperlipoproteinemia Type II.

Browse Hyperlipoproteinemia Type II studies →

Lead sponsor

Geisinger Clinic is the lead sponsor of 125 studies on the registry; 21 are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 7 (78%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
26 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Primary care clinicians (pediatrician, community medicine, internal medicine) in the Geisinger Healthcare System

Exclusion criteria

Exclusion Criteria:

  • None
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
532 participants (estimated)

Study arms

  • Other
    Phase 1

    Phased rollout to clinic sites across the the Geisinger system using stepped wedge design

    Behavioral: FH diagnosis program · Behavioral: Implementation strategy package: Develop and implement tools for quality monitoring · Behavioral: Implementation strategy package: Develop educational materials · Behavioral: Implementation strategy package: Conduct educational outreach visits · Behavioral: Implementation strategy package: Intervene with clinicians and patients to enhance · Behavioral: Behavioral (e.g., Psychotherapy, Lifestyle Counseling) Implementation strategy package: Identify and prepare champions Clinical lipid champions · Behavioral: Implementation strategy package: Audit and provide feedback · Behavioral: Implementation strategy package: Stage implementation scale up

  • Other
    Phase 2

    Phased rollout to clinic sites across the the Geisinger system using stepped wedge design

    Behavioral: FH diagnosis program · Behavioral: Implementation strategy package: Develop and implement tools for quality monitoring · Behavioral: Implementation strategy package: Develop educational materials · Behavioral: Implementation strategy package: Conduct educational outreach visits · Behavioral: Implementation strategy package: Intervene with clinicians and patients to enhance · Behavioral: Behavioral (e.g., Psychotherapy, Lifestyle Counseling) Implementation strategy package: Identify and prepare champions Clinical lipid champions · Behavioral: Implementation strategy package: Audit and provide feedback · Behavioral: Implementation strategy package: Stage implementation scale up

  • Other
    Phase 3

    Phased rollout to clinic sites across the the Geisinger system using stepped wedge design

    Behavioral: FH diagnosis program · Behavioral: Implementation strategy package: Develop and implement tools for quality monitoring · Behavioral: Implementation strategy package: Develop educational materials · Behavioral: Implementation strategy package: Conduct educational outreach visits · Behavioral: Implementation strategy package: Intervene with clinicians and patients to enhance · Behavioral: Behavioral (e.g., Psychotherapy, Lifestyle Counseling) Implementation strategy package: Identify and prepare champions Clinical lipid champions · Behavioral: Implementation strategy package: Audit and provide feedback · Behavioral: Implementation strategy package: Stage implementation scale up

  • Other
    Phase 4

    Phased rollout to clinic sites across the the Geisinger system using stepped wedge design

    Behavioral: FH diagnosis program · Behavioral: Implementation strategy package: Develop and implement tools for quality monitoring · Behavioral: Implementation strategy package: Develop educational materials · Behavioral: Implementation strategy package: Conduct educational outreach visits · Behavioral: Implementation strategy package: Intervene with clinicians and patients to enhance · Behavioral: Behavioral (e.g., Psychotherapy, Lifestyle Counseling) Implementation strategy package: Identify and prepare champions Clinical lipid champions · Behavioral: Implementation strategy package: Audit and provide feedback · Behavioral: Implementation strategy package: Stage implementation scale up

  • Other
    Phase 5

    Phased rollout to clinic sites across the the Geisinger system using stepped wedge design

    Behavioral: FH diagnosis program · Behavioral: Implementation strategy package: Develop and implement tools for quality monitoring · Behavioral: Implementation strategy package: Develop educational materials · Behavioral: Implementation strategy package: Conduct educational outreach visits · Behavioral: Implementation strategy package: Intervene with clinicians and patients to enhance · Behavioral: Behavioral (e.g., Psychotherapy, Lifestyle Counseling) Implementation strategy package: Identify and prepare champions Clinical lipid champions · Behavioral: Implementation strategy package: Audit and provide feedback · Behavioral: Implementation strategy package: Stage implementation scale up

Interventions

  • BehavioralFH diagnosis program

    Uptake of screening, diagnosis, and initiation of care management for FH

  • BehavioralImplementation strategy package: Develop and implement tools for quality monitoring

    EHR tools to order labs, record results, and document FH care

  • BehavioralImplementation strategy package: Develop educational materials

    Education regarding guidelines for identification and treatment of FH

  • BehavioralImplementation strategy package: Conduct educational outreach visits

    Continuing medical education (CME) material for FH that is presented to

  • BehavioralImplementation strategy package: Intervene with clinicians and patients to enhance

    Notify patients simultaneously with clinicians about the need for screening

  • BehavioralBehavioral (e.g., Psychotherapy, Lifestyle Counseling) Implementation strategy package: Identify and prepare champions Clinical lipid champions

    Clinical lipid champions

  • BehavioralImplementation strategy package: Audit and provide feedback

    Provide aggregate level feedback to clinics on diagnosing FH

  • BehavioralImplementation strategy package: Stage implementation scale up

    Develop the timeline for the stepped-wedge rollout to primary care

06

What researchers measure

Primary outcomes

  1. FH diagnosis rate (Aim 2)

    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

    Time frame: Up to 45 months

  2. Acceptability (Aim 3)

    Clinician and patient satisfaction and self-efficacy with the FH diagnosis program

    Time frame: Month 9, 12, 18, 24, 30, 36, 42

  3. Timeliness (Aim 4)

    Time to FH screen, time to diagnostic evaluation, time to statin initiation

    Time frame: Up to 45 months

Secondary outcomes

  1. Initiation medication use (Aim 2)

    Initiation of lipid lowering medication by healthcare clinician

    Time frame: Up to 45 months

  2. Lipid measurement (Aim 2)

    Order of a lipid panel

    Time frame: Up to 45 months

  3. Genetic testing (Aim 2)

    Order of a genetic test for FH

    Time frame: Month 9, 12, 18, 24, 30, 36, 42

  4. Problem list diagnosis of FH (Aim 2)

    Clinician adds diagnosis of FH to the patients problem list in the electronic health record

    Time frame: Up to 45 months

  5. FH smartset (Aim 2)

    Clinician uses and completes all field of the FH smartset

    Time frame: Month 9, 12, 18, 24, 30, 36, 42

  6. Best Practice Alert (Aim 2)

    Clinician adheres to and acts on recommendation in the Best Practice Alert

    Time frame: Up to 45 months

  7. FH Clinic Note (Aim 2)

    Clinician completes the FH clinic note

    Time frame: Up to 45 months

  8. Fidelity (Aim 3)

    Documentation of adaptations to the FH diagnosis program

    Time frame: Up to 45 months

  9. Cost (Aim 3)

    Cost to implement the implementation strategy package

    Time frame: Up to 45 months

  10. Function (Aim 4)

    Return of genetic result to patient (if ordered and patient undergoes testing)

    Time frame: Up to 45 months

  11. Function (Aim 4)

    Reduction in lipid level from baseline to end of the study period

    Time frame: Up to 45 months

  12. Function (Aim 4)

    Patient side effects to medications

    Time frame: Up to 45 months

07

Study locations

1 site
  • Geisinger Clinic
    Multiple Locations, Pennsylvania 00000, United States
08

References and documents

Publications

  • Jones LK, Romagnoli KM, Schubert TJ, Clegg K, Kirchner HL, Hu Y, Cawley D, Norelli V, Williams MS, Gidding SS, Rahm AK. Using implementation science to develop a familial hypercholesterolemia screening program in primary care: The CARE-FH study. J Clin Lipidol. 2024 Mar-Apr;18(2):e176-e188. doi: 10.1016/j.jacl.2024.01.001. Epub 2024 Jan 4. PubMed 38228467 ↗

Individual participant data

Plan to share: No — Available upon request from PIs

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 22, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05284513
Lead sponsor
Geisinger Clinic
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
Responsible party
Samuel Gidding (Professor, Geisinger Clinic) — Principal investigator
First posted
Mar 17, 2022
Start date
Sep 9, 2022
Primary completion
Jan 2027 (estimated)
Completion
Jan 2027 (estimated)
Last update
Dec 22, 2025

Study contacts

Laney K Jones, PharmD, MPH
principal investigator · Geisinger Clinic
Samuel S Gidding, MD
principal investigator · Geisinger Clinic

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

No contact was published for this record. The registry link below has the sponsor’s details.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion