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Improved Cardiovascular Risk Reduction to Enhance Rural Primary Care (ICARE)

K

Korey Kennelty

Status

Completed

Conditions

Coronary Artery Disease
Hypertension
Atrial Fibrillation
Stroke
Diabetes Mellitus

Treatments

Other: Personal Health Record
Other: PHCVRS Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT01983813
201308707

Details and patient eligibility

About

The trial will examine whether a centralized Prevention Health & Cardiovascular Risk Service (PHCVRS) run by clinical pharmacists at the University of Iowa can be implemented in primary care offices and whether it can improve the care delivered to patients at risk for developing cardiovascular disease.

Full description

The use of clinical pharmacists in primary care has improved the control of several chronic cardiovascular conditions. However, many private physician practices lack the resources to implement team-based care with pharmacists. The purpose of this study was to evaluate whether a centralized, remote, clinical pharmacy service could improve guideline adherence and secondary measures of cardiovascular risk in primary care offices in rural and small communities.

This study was a prospective trial in 12 family medicine offices cluster randomized to either the intervention or usual care. The intervention was delivered for 12 months, and subjects had research visits at baseline and 12 months. The primary outcome was adherence to guidelines, and secondary outcomes included changes in key cardiovascular risk factors and preventative health measures. We enrolled 302 subjects.

Enrollment

302 patients

Sex

All

Ages

50+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

INCLUSION CRITERIA

Section A: Demographic Criteria

  1. Patient was seen in your clinic or practice at least once in the past 24 months

  2. English-speaking male or female

  3. Age is 50 or older at medical record screening

    Section B: Risk Factors - Must have at least one of the following conditions

  4. Uncontrolled diabetes (Hemoglobin A1c > or + 7.5)

  5. Elevated LDL cholesterol > 110 for patients with PAD, CAD, stroke or diabetes or > 140 otherwise

  6. Elevated blood pressure with:

    • Systolic BP >= 140 or Diastolic BP >=90 in persons with diabetes or chronic kidney disease OR
    • Systolic BP >= 150 in persons with uncomplicated hypertension

    Section C: Cardiovascular Conditions - total number of risk factors in Section B (above) plus number of conditions Section C (below) must be THREE OR MORE

  7. History of coronary artery disease

  8. Previous Heart Attack

  9. History of Stroke

  10. History of Transient Ischemic Attack

  11. History of Atrial fibrillation

  12. History of Peripheral Vascular Disease / claudication

  13. History of carotid artery disease

  14. Current smoker

  15. Obesity with BMI > 30

    EXCLUSION CRITERIA

    Section D: Exclusion Criteria - has NONE of the following:

  16. Inability to give informed consent

  17. Pregnant

  18. Diagnosis of pulmonary hypertension (Note: secondary pulmonary hypertension is OK)

  19. Cancer diagnosis with a life expectancy estimated less than 2 years

  20. Residence in a nursing home or diagnosis of dementia

  21. No telephone or a hearing impairment not allowing them to use a phone

  22. Refusal to consider attempting to use the internet at home, community center, library, medical office or other source to access the PHRM

  23. Patient has plans to move from the area or transfer care to a different clinic in the next 12 months

  24. Omron blood pressure cuff cannot be used on patient's arm for any reason

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

302 participants in 2 patient groups

PHCVRS intervention
Experimental group
Description:
Each participant will receive communication with a clinical pharmacist for 12 months to decrease risk of developing cardiovascular disease.
Treatment:
Other: Personal Health Record
Other: PHCVRS Intervention
Usual care/Personal Health Record
Other group
Description:
Will receive usual medical care plus access to an online Personal Health Record, where the participant can document medications and diagnosed conditions.
Treatment:
Other: Personal Health Record

Trial contacts and locations

12

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Data sourced from clinicaltrials.gov

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