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Sponsor study identifier
observational
148
1 country
1
Study Start
January 2013
Date type not reportedThis date has not been verified as actual or estimated.
Primary Completion
June 2017
Actual (reported)Study Completion
December 2017
Actual (reported)The Physical Functioning Inventory (PFI) is a standardized patient reported outcome measure that assesses preclinical disability. Preclinical disability is a functional state in which people are still able to complete daily living tasks (e.g., walking, bathing) but are changing the frequency or modifying the way that they complete the tasks. The investigators have done some preliminary research using the PFI as an online monitoring tool (Richardson 2012), but further study is required to examine its psychometric properties and its suitability for use as a primary outcome measure. This measurement study has been designed to identify the optimal number of items on the PFI and to determine the reliability, validity, and responsiveness of the PFI when administered to a sample of adults and older adults both with and without chronic conditions. This project will also allow us to evaluate the use of self-monitoring of physical function and the added value of rehabilitation professionals to support self-monitoring. Using the results of the PFI, the investigators aim to develop a "tailored" population-based rehabilitation self-management intervention delivered through a secure messaging system in the patient's electronic personal health record (myOSCAR) that focuses on the early detection and prevention of preclinical disability.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
December 2017
Actual (reported)Click on a node to explore related trials.
Some registry-reported names shown below are not yet linked in this graph.
Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
January 2013
Date type not reportedThis date has not been verified as actual or estimated.
May 14, 2013
Actual (reported)November 8, 2013
Actual (reported)June 2017
Actual (reported)December 2017
Actual (reported)Physical Functioning Inventory
The PFI will be administered at baseline, then again 3-5 days later to assess test-retest reliability. It will then be administered at 6 months, 12 months and 18 months to determine its longitudinal validity. It will be administered a final time 3-5 days after the 18 month time frame to re-evaluate the measures test-retest reliability.
Baseline, 3-5 days later, 6 months, 12 months, 18 months, 3-5 days later
Mobility Survey
Baseline, 3-5 days later, 6 months, 12 months, 18 months, 3-5 days later
The Rapid Assessment of Physical Activity (RAPA)
Baseline, 3-5 days later, 6 months, 12 months, 18 months, 3-5 days later
Participants greater than or equal to 44 years of age with a chronic disease (diabetes, heart disease, stroke, hypertension, osteoporosis, osteoarthritis, rheumatoid arthritis, chronic obstructive pulmonary disease, back pain, Multiple Sclerosis, Parkinson's Disease).
Participants greater than or equal to 65 years of age without a chronic disease.
Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.
Primary care center
Stonechurch Family Health Centre
Hamilton, Ontario, L8W 3L2, Canada
Julie Richardson, PhD
McMaster University
Lori Letts, PhD
McMaster University
148 participants (actual enrollment reported by the registry).
First Submitted
May 14, 2013
First Posted
November 8, 2013
Study Start
January 2013
Date type not reportedThis date has not been verified as actual or estimated.
Patient Specific Functional Scale (PSFS)
Baseline, 18 months
Center for Epidemiological Studies Depression Scale (CESD-R)
Baseline, 18 months
Brief Pain Inventory
Baseline, 18 months
Contact the study team to confirm eligibility.
Primary Completion
June 2017
Actual (reported)Study Completion
December 2017
Actual (reported)Last Updated
April 9, 2018
Record last verified: 2018-04
Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.
Source: ClinicalTrials.gov.
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