Chronic Illness Care Management (CICM) Study In Primary Care

NCT ID: NCT00153829

Last Updated: 2015-02-23

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

PHASE1

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2004-12-31

Study Completion Date

2006-02-28

Brief Summary

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The purpose of the study is to determine whether the quality of life of patients with multiple chronic conditions cared for by primary care physicians will improve due to the introduction of a chronic illness management intervention.

Detailed Description

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There is international recognition for the need of introducing improvement in chronic illness care. However, primary care physicians face a host of challenges for providing the best possible care to their patients. One of these problems is the lack of proper administrative systems. There is evidence indicating that tailored out reach facilitation is an effective means to improve practice performance. Traditionally, the approach to care for chronically ill patients revolved mostly around the treatment of a specific chronic condition in an ad hoc basis. It is more common in family medicine for the patient to have several chronic conditions. There is also evidence showing that better health outcomes are obtained when the patients' life circumstances, desires and expectations are taken into consideration. Various models of chronic illness care have emerged that are patient center while attempting to be comprehensive. Our approach, following the Australian model, seeks to introduce systems/administrative innovations at the practice level, intended also to increase the involvement of patients with multiple chronic conditions on its own care, throw tailored out reach facilitation and care planning tools for physicians, in order to improve chronic illness management in primary care settings.

Conditions

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Chronic Illness Quality of Life

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Interventions

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Multifaceted outreach facilitation for chronic illness care

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Patient should suffer from any two or more chronic illnesses
* Patient should have been seen in the GP's office at least six to seven times in the previous year
* Patient should be 50 years of age or older

Exclusion Criteria

* Suffering from dementia or a major psychiatric condition, being terminally ill, not being competent to give informed consent for participating in the study, or the doctors considers that the patient will not benefit from the intervention.
Minimum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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C. T. Lamont Primary Care Research Centre

OTHER

Sponsor Role lead

Principal Investigators

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William Hogg, MD, CCFP

Role: PRINCIPAL_INVESTIGATOR

University of Ottawa

Jacques Lemelin, MD, CCFP

Role: PRINCIPAL_INVESTIGATOR

University of Ottawa

Locations

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University of Ottawa, Institute of Population Health

Ottawa, Ontario, Canada

Site Status

Countries

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Canada

Other Identifiers

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T-0528-029-22-CICM

Identifier Type: -

Identifier Source: org_study_id

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