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NCT00238836 Clinical Trial

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

Hypertension Clinical Trial

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00238836
Other study ID # APTCare
Secondary ID
Status Active, not recruiting
Phase Phase 2/Phase 3
First received October 12, 2005
Last updated October 12, 2006
Est. completion date March 2006

Study information
Verified date June 2005
Source C. T. Lamont Primary Care Research Centre
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 240
Est. completion date March 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 50 Years and older
Eligibility 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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Behavioral:
• Self-management of chronic illness

Locations
Country Name City State
Canada West Carleton Family Health Network Carp Ontario

Sponsors (3)
Lead Sponsor Collaborator
C. T. Lamont Primary Care Research Centre Ontario Ministry of Health and Long Term Care, University of Ottawa

Country where clinical trial is conducted

Canada, 

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