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Collaborative Cardiac Care Project (C3P)

US Department of Veterans Affairs (VA) logo

US Department of Veterans Affairs (VA)

Status

Completed

Conditions

Myocardial Ischemia
Angina Pectoris
Coronary Disease

Treatments

Procedure: Group interventions
Procedure: Collaborative care model
Procedure: Facilitated consultation

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT00105664
IHI 02-062

Details and patient eligibility

About

Data from VA-funded studies and the broader literature indicate that chronic stable angina (CSA) is prevalent, under recognized, under treated and associated with reduced quality of life. There are substantial opportunities for improving care of patients with this debilitating and potentially fatal problem. Because primary care providers manage most patients with CSA, efforts to improve care must necessarily involve the primary care delivery system. C3P is composed of a set of interventions employing a Collaborative Care Team model, which has been shown to be effective in managing other chronic illnesses in the primary care setting.

Full description

Objectives of the proposed project are to: 1) ascertain whether a collaborative approach to managing CSA in primary care results in better symptom control and quality of life than routine care; 2) assess whether the practice of providers assigned to the intervention group is more consistent with national clinical practice guidelines than that of control providers; 3) assess satisfaction of both patients and providers with this approach to management; and 4) assess marginal cost-effectiveness.

Enrollment

287 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Providers:

  • Staff (MD, PA, NP) or resident (R1, R2)
  • at least 1 participating patient

Patients

  • assigned to participating provider
  • diagnosis consistent with IHD
  • 2 visits in past year
  • frequent angina symptoms (SAQ freq. score less than 70)

Exclusion criteria

Providers:

  • No participating patients

Patients:

  • cognitive impairment (inability to complete questionnaires and phone interviews)
  • non-participating provider
  • life expectancy of less than 24 months

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

287 participants in 1 patient group

Arm 1
Other group
Treatment:
Procedure: Collaborative care model
Procedure: Group interventions
Procedure: Facilitated consultation

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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