Collaborative Cardiac Care Project

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

287 participants

Study Classification

INTERVENTIONAL

Study Start Date

2004-10-31

Study Completion Date

2007-07-31

Brief Summary

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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.

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Detailed Description

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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.

Conditions

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Myocardial Ischemia Angina Pectoris Coronary Disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Arm 1

Group Type OTHER

Collaborative care model

Intervention Type PROCEDURE

Group interventions

Intervention Type PROCEDURE

Facilitated consultation

Intervention Type PROCEDURE

Interventions

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Collaborative care model

Intervention Type PROCEDURE

Group interventions

Intervention Type PROCEDURE

Facilitated consultation

Intervention Type PROCEDURE

Eligibility Criteria

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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

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No