Collaborative Cardiac Care Project (C3P)
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ClinicalTrials.gov Identifier: NCT00105664 |
Recruitment Status
:
Completed
First Posted
: March 17, 2005
Last Update Posted
: April 7, 2015
|
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Myocardial Ischemia Angina Pectoris Coronary Disease | Procedure: Collaborative care model Procedure: Group interventions Procedure: Facilitated consultation | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 287 participants |
Allocation: | Randomized |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Collaborative Cardiac Care Project (C3P) |
Study Start Date : | October 2004 |
Actual Study Completion Date : | July 2007 |
Arm | Intervention/treatment |
---|---|
Arm 1 | Procedure: Collaborative care model Procedure: Group interventions Procedure: Facilitated consultation |
- Symptom control, quality of life and satisfaction at one year; improved practitioner compliance with national clinical practice guidelines over the one-year intervention period
- Marginal cost effectiveness during one-year study period

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Ages Eligible for Study: | 18 Years and older (Adult, Senior) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
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

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00105664
United States, California | |
VA Palo Alto Health Care System, Palo Alto, CA | |
Palo Alto, California, United States, 94304-1290 | |
United States, Colorado | |
VA Eastern Colorado Health Care System, Denver, CO | |
Denver, Colorado, United States, 80220 | |
United States, Oregon | |
VA Portland Health Care System, Portland, OR | |
Portland, Oregon, United States, 97239 | |
United States, Washington | |
VA Puget Sound Health Care System Seattle Division, Seattle, WA | |
Seattle, Washington, United States, 98108 |
Principal Investigator: | Stephan D. Fihn, MD MPH | VA Puget Sound Health Care System Seattle Division, Seattle, WA |
Publications of Results:
Responsible Party: | VA Office of Research and Development |
ClinicalTrials.gov Identifier: | NCT00105664 History of Changes |
Other Study ID Numbers: |
IHI 02-062 |
First Posted: | March 17, 2005 Key Record Dates |
Last Update Posted: | April 7, 2015 |
Last Verified: | October 2007 |
Keywords provided by VA Office of Research and Development:
Outcomes Assessment Primary Health Care Group Process |
Additional relevant MeSH terms:
Ischemia Coronary Disease Coronary Artery Disease Myocardial Ischemia Angina Pectoris Pathologic Processes Heart Diseases Cardiovascular Diseases |
Vascular Diseases Arteriosclerosis Arterial Occlusive Diseases Chest Pain Pain Neurologic Manifestations Nervous System Diseases Signs and Symptoms |