Anticipatory & Preventive Team Care (APTCare): At Risk Patients of Family Health Networks
Primary Purpose
Diabetes, Chronic Obstructive Pulmonary Disease, Congestive Heart Failure
Status
Unknown status
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Self-management of chronic illness
Sponsored by
About this trial
This is an interventional prevention trial for Diabetes
Eligibility Criteria
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
Sites / Locations
- West Carleton Family Health Network
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00238836
First Posted
October 12, 2005
Last Updated
October 12, 2006
Sponsor
C. T. Lamont Primary Care Research Centre
Collaborators
Ontario Ministry of Health and Long Term Care, University of Ottawa
1. Study Identification
Unique Protocol Identification Number
NCT00238836
Brief Title
Anticipatory & Preventive Team Care (APTCare): At Risk Patients of Family Health Networks
Study Type
Interventional
2. Study Status
Record Verification Date
June 2005
Overall Recruitment Status
Unknown status
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 2006 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
C. T. Lamont Primary Care Research Centre
Collaborators
Ontario Ministry of Health and Long Term Care, University of Ottawa
4. Oversight
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes, Chronic Obstructive Pulmonary Disease, Congestive Heart Failure, Hypertension
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
240 (false)
8. Arms, Groups, and Interventions
Intervention Type
Behavioral
Intervention Name(s)
Self-management of chronic illness
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William Hogg, MD
Organizational Affiliation
C. T. Lamont Primary Care Research Centre
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jacques Lemelin, MD
Organizational Affiliation
University of Ottawa
Official's Role
Principal Investigator
Facility Information:
Facility Name
West Carleton Family Health Network
City
Carp
State/Province
Ontario
ZIP/Postal Code
K0A 1L0
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
22893340
Citation
Fletcher J, Hogg W, Farrell B, Woodend K, Dahrouge S, Lemelin J, Dalziel W. Effect of nurse practitioner and pharmacist counseling on inappropriate medication use in family practice. Can Fam Physician. 2012 Aug;58(8):862-8.
Results Reference
derived
PubMed Identifier
20154234
Citation
Dahrouge S, Hogg W, Lemelin J, Liddy C, Legault F. Methods for a study of Anticipatory and Preventive multidisciplinary Team Care in a family practice. Can Fam Physician. 2010 Feb;56(2):e73-83.
Results Reference
derived
PubMed Identifier
20090057
Citation
Gray D, Armstrong CD, Dahrouge S, Hogg W, Zhang W. Cost-effectiveness of Anticipatory and Preventive multidisciplinary Team Care for complex patients: evidence from a randomized controlled trial. Can Fam Physician. 2010 Jan;56(1):e20-9.
Results Reference
derived
PubMed Identifier
20008582
Citation
Hogg W, Lemelin J, Dahrouge S, Liddy C, Armstrong CD, Legault F, Dalziel B, Zhang W. Randomized controlled trial of anticipatory and preventive multidisciplinary team care: for complex patients in a community-based primary care setting. Can Fam Physician. 2009 Dec;55(12):e76-85.
Results Reference
derived
Learn more about this trial
Anticipatory & Preventive Team Care (APTCare): At Risk Patients of Family Health Networks
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