Rehabilitation in Primary Care: A Project to Maximize the Health Status of Adults With Chronic Illness

July 13, 2010 updated by: Hamilton Health Sciences Corporation
The purpose of the study is to determine whether occupational therapy and physiotherapy delivered in a primary care setting to adults with chronic illness is effective in improving health.

Study Overview

Detailed Description

Primary health care is changing so that people receive the care that they need at the front line. Rehabilitation has been identified as one service that should be offered in primary care, to address the needs of adults who have or are at risk of poor health from chronic conditions such as arthritis, heart disease and depression.

Two full time therapists (one physiotherapist and one occupational therapist) will offer rehabilitation to a sample of 170 adults with chronic illness over an 18 month period (170 people will also be enrolled in a control group) at the Stonechurch Family Health Centre. Key outcomes include health, hospital admissions and emergency room visits.

Study Type

Interventional

Enrollment (Actual)

303

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 3L2
        • Stonechurch Family Health Centre, 549 Stonechurch Rd. E.

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:

  • At least 1 chronic condition
  • 3 visits to family physician in the past year

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention
No Intervention: Control
Control group received usual care in primary care.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
SF-36 Physical Component
Time Frame: 15 months
health related quality of life. Minimum: 0; Maximum 100.
15 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Use of Hospital Services
Time Frame: baseline, 15 months
self report use of hospital service
baseline, 15 months
Independence in Activities of Daily Living (ADLs) and Instrumental Activities of Daily Living (IADLs)
Time Frame: baseline, 15 months
Late Life Function and Disability Instrument: A measure of disability and functional limitations in older adults. (Score range 0-100 with 100 representing better ability and less disability/functional limitation)
baseline, 15 months
Functional Limitations
Time Frame: baseline, 15 months
Late Life Function and Disability Instrument: A measure of functional limitations and disability in older adults.
baseline, 15 months
Falls and Injuries
Time Frame: baseline, 15 months
self-reported number of falls in last 6 months
baseline, 15 months
HOME Falls and Accident Screening Tool (FAST)
Time Frame: baseline, 15 months
This is a home assessment of safety hazards for falls present in the individual's home. This tool helps to identify seniors at risk of falls. Score 0-25.
baseline, 15 months
Self-management and Self-efficacy
Time Frame: baseline, 15 months
Individual's self-reported ability to carry out behaviours to self-manage their health condition, and their confidence level in being able to carry out these behaviours. (Score range 0= not confident at all, 10= totally confident).
baseline, 15 months
Physical Abilities (Strength, Balance)
Time Frame: baseline, 15 months
Grip strength was measured using a JAMAR hand grip dynamometer (in kilograms). The Lower Extremity Function test is a battery of three tests used to measure lower extremity function and balance: a balance test, 8 foot walk test, and repetitive standing from a chair. A performance summary score is created by adding the number of seconds achieved on the balance test, the number of seconds to walk 8 feet and the number of seconds it takes the person to stand up from a chair five times consecutively (no maximum score exists on this measure).
baseline, 15 months
Patient Satisfaction Questionnaire - 18 (Modified)
Time Frame: 15 months
Patient satisfaction with the care they received. (Score range 0-5)
15 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Julie Richardson, PhD, McMaster University
  • Principal Investigator: Lori Letts, PhD, McMaster University

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

June 1, 2004

Primary Completion (Actual)

August 1, 2006

Study Completion (Actual)

October 1, 2006

Study Registration Dates

First Submitted

September 28, 2005

First Submitted That Met QC Criteria

September 28, 2005

First Posted (Estimate)

September 30, 2005

Study Record Updates

Last Update Posted (Estimate)

July 20, 2010

Last Update Submitted That Met QC Criteria

July 13, 2010

Last Verified

September 1, 2009

More Information

Terms related to this study

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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