- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00859638
I Am Able: Population Based Rehabilitation in a Family Health Team
June 17, 2010 updated by: Hamilton Health Sciences Corporation
People who have long-term conditions such as heart disease, diabetes, arthritis etc. face challenges in staying active and able to participate in activities that are important to them.
There is some research that suggests that a care model that focuses on physical functioning and helping patients to manage their own conditions will assist them to stay active and healthy longer.
In this project, the investigators are testing whether physiotherapy and occupational therapy offered to groups of patients and information about rehabilitation offered to other members of the health care team can help people with chronic conditions to maintain their physical abilities.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Participants older than 44, with at least one chronic disease, (n=60) will participate in a before-and-after study integrating a population based, rehabilitation-focused program targeting physical function into a Family Health Team.
The program, delivered by a Physiotherapist and Occupational Therapist, will consist of comprehensive functional assessments and individualized self-management care plans; a rehabilitation based chronic disease self-management program; and on-line self-monitoring of physical function.
Process and outcome measures will be administered at baseline and 4 months follow-up.
Study Type
Interventional
Enrollment (Actual)
124
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ontario
-
Hamilton, Ontario, Canada, L8W 3J6
- McMaster Family Health Team (Stonechurch Family Health Centre and McMaster Family Practice)
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
44 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 44 years and older
- 1 or more chronic conditions
- 3 visits to physician in the past year
- access or willingness to access email
Exclusion Criteria:
- none
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention Group
Rehabilitation self-management group, on-line self monitoring of physical function, and organizational capacity building.
|
group self-management classes
group self-management classes
workshops and case reviews with primary health care team members
|
|
No Intervention: Case matched controls
Usual care in primary health care.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Physical Functioning Inventory (PFI)
Time Frame: 4 months
|
The PFI is used to assess physical functioning in older adults.
It contains 21 tasks from 4 subscales: activities of daily living, instrumental activities of daily living, mobility, moderate activities.
A series of questions is used to determine whether the person experiences difficulty in completing a task, the level of difficulty they experience, and any changes to the method and/or frequency of task performance.
The PFI is sensitive to steps in the natural history of functional decline that are often not assessed clinically.
Range of scores: 0 (most difficulty); 100 (least difficulty).
|
4 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Self-rated Health
Time Frame: 4 months
|
4 months
|
|
Health Care Utilization
Time Frame: 4 months
|
4 months
|
|
Self-efficacy for Chronic Disease Scale
Time Frame: 4 months
|
4 months
|
|
Rapid Assessment of Physical Activity
Time Frame: 4 months
|
4 months
|
|
Grip Strength
Time Frame: 4 months
|
4 months
|
|
Two Minute Walk Test
Time Frame: 4 months
|
4 months
|
|
Patient Assessment of Chronic Illness Care
Time Frame: 4 months
|
4 months
|
|
Primary Care Resources and Supports
Time Frame: 4 months
|
4 months
|
|
Balance Screen
Time Frame: 4 months
|
4 months
|
|
Eight Foot Walk Test
Time Frame: 4 months
|
4 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Julie Richardson, PhD, McMaster University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2008
Primary Completion (Actual)
March 1, 2009
Study Completion (Actual)
April 1, 2009
Study Registration Dates
First Submitted
March 10, 2009
First Submitted That Met QC Criteria
March 10, 2009
First Posted (Estimate)
March 11, 2009
Study Record Updates
Last Update Posted (Estimate)
June 22, 2010
Last Update Submitted That Met QC Criteria
June 17, 2010
Last Verified
September 1, 2009
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 08-177
- 2007-ORRAN-IIA-568
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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