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Anticipatory & Preventive Team Care (APTCare): At Risk Patients of Family Health Networks

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00238836
Enrollment
240
Registered
2005-10-14
Start date
Unknown
Completion date
2006-03-31
Last updated
2006-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease, Congestive Heart Failure, Diabetes, Hypertension

Brief summary

The University of Ottawa and Élisabeth Bruyère Research Institute are conducting a study of preventive care for frail patients at risk of functional decline. At risk patients are assigned by chance to continue receiving their standard care from their family physician or receive additional care from a nurse practitioners and a pharmacist. In collaboration with the family physician, they develop an individualized care plan, a treatment and management road plan, for each patient, which they implement over the study period of one approximately year. The objective of the study is to compare the effectiveness of the model of care that includes the nurse practitioners and pharmacist against standard care in preventing functional decline, to determine the acceptability of this model of care to patients, their caregivers and the medical team, and to evaluate the cost implication of the program.

Interventions

BEHAVIORALSelf-management of chronic illness

Sponsors

Ontario Ministry of Health and Long Term Care
CollaboratorOTHER_GOV
University of Ottawa
CollaboratorOTHER
C. T. Lamont Primary Care Research Centre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 50 years and over * 'At Risk' by having one or more of the following: a. Visits to emergency dept within the past 6 months; b. Admission to hospital for a medical problem in past 6 months; c. High service use profiles; d. Polypharmacy; e. Other high risk factors * Capable of giving informed consent * Able to use the Care Companion technology

Exclusion criteria

* Cognitive impairment such that they cannot give informed consent * Unable or unwilling to use the telehomecare equipment * Unlikely to tolerate the intensive intervention * Language or cultural barriers * Being acutely ill or having an unstable condition on entry to the study

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026