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Pharmacist-initiated Intervention Trial in OsteoArthritis (PhIT-OA)

Primary Purpose

Knee Osteoarthritis

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Pharmacist-Initiated Intervention in OsteoArthritis (PhIT-OA)
Sponsored by
University of British Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Knee Osteoarthritis focused on measuring Pharmacist-initiated Intervention Trial in OsteoArthritis

Eligibility Criteria

50 Years - 95 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age >50 years
  2. ≥ 4 weeks of pain, aching or discomfort in or around the knee
  3. Overweight or obese defined as BMI defined as ≥ 27 kg/m2
  4. Not actively participating in a formal exercise program within the past 6 months
  5. Self-reported difficulty in at least one of the following activities attributed to knee pain: lifting and carrying groceries, walking one quarter of a mile, getting in and out of a chair, or going up and down stairs.
  6. Meet eligibility using the criteria on the pharmacist screening form (see attachment) - This form was adapted from the PhIND-OA study and amended to include points #3 to 6 above.

Exclusion Criteria:

  1. Significant co-morbid disease that would pose a safety threat or impair ability to participate in an exercise program
  2. Inability or unwillingness to modify dietary or exercise behaviours.
  3. Knee X-Ray within the last 2 years
  4. Inability to speak and write English
  5. Knee pain due only to referred pain from osteoarthritis of the hip

Sites / Locations

  • Mary Pack Arthritis Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Health service provision

Arm Description

Health service provision within the first few months of diagnosis which includes physical examination, radiographs, education, exercise, weight loss, assistive devices and pharmacologic therapy.

Outcomes

Primary Outcome Measures

The primary outcome will be the difference in proportion of patients who receive ≥ 5 of the Arthritis Foundation's quality indicators during the six months of the study.
(Baseline, months 2 and 6 )

Secondary Outcome Measures

There are four secondary outcome measures that will be compared between intervention and usual care subjects at baseline, months 2 and 6:
The difference in change of physical functioning (using the mean score from 17 questions from the WOMAC that are directed towards this construct) between intervention and usual care. This outcome has been used in recent, well-designed trials of OA.
The difference in knee pain (as assessed by five questions on the WOMAC);
The difference in Health Utilities Index Mark 3 (HUI3); and
The direct medical resource utilization using a questionnaire validated for use in musculoskeletal diseases.

Full Information

First Posted
October 24, 2006
Last Updated
March 14, 2014
Sponsor
University of British Columbia
Collaborators
Canadian Institutes of Health Research (CIHR), Canadian Arthritis Network, Michael Smith Foundation for Health Research
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1. Study Identification

Unique Protocol Identification Number
NCT00391859
Brief Title
Pharmacist-initiated Intervention Trial in OsteoArthritis (PhIT-OA)
Official Title
Pharmacist-initiated Intervention Trial in OsteoArthritis (PhIT-OA)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
September 2006 (undefined)
Primary Completion Date
June 2010 (Actual)
Study Completion Date
June 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of British Columbia
Collaborators
Canadian Institutes of Health Research (CIHR), Canadian Arthritis Network, Michael Smith Foundation for Health Research

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Osteoarthritis (OA) is a major public health concern. Currently, there are at least 3 million Canadians afflicted with this condition with a 50% increase predicted by 2020. It is estimated that 85% of Canadians are afflicted with OA by age 70. As such, using the current health care structure, it is doubtful that the health system can keep pace with this increasing demand. Alternative health care delivery strategies must be investigated. The purpose of this study is to assess if a pharmacist-initiated intervention for individuals with knee pain with a high likelihood of knee OA will lead to an improvement in the quality of care for these individuals. We are hopeful that results of this study will show better management of knee osteoarthritis by a pharmacist-initiated intervention (which means that it is the pharmacist who will start the process for an intervention that includes exercise and an educational program when compared to no intervention. If this is the case, by implementing the proposed intervention program, subjects could be diagnosed earlier, the burden of illness on individuals could be diminished through an appropriate intervention program, and economic savings could be embraced. Hypothesis: Community pharmacists can identify patients with likely knee OA and initiate a multidisciplinary intervention that will improve quality of care and outcomes.
Detailed Description
This will be a pilot study of a multidisciplinary intervention for individuals with knee pain with a high likelihood of knee OA that could be a model for other chronic diseases. The intervention will be multidisciplinary such that it will be initiated by community pharmacists with referral to a comprehensive OA treatment program at the provincial arthritis center involving physiotherapists. In addition, formal communication will be initiated with their family doctor. Those in the usual care group will receive an educational OA pamphlet. The primary objective of this pilot project is to determine the proportion of patients who meet the Arthritis Foundation's Quality Indicator Set for osteoarthritis in the treatment arm compared to those in the usual care arm. Specifically, this indicator set focuses on health service provision within the first few months of diagnosis which includes physical examination, radiographs, education, exercise, weight loss, assistive devices and pharmacologic therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
Keywords
Pharmacist-initiated Intervention Trial in OsteoArthritis

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
135 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Health service provision
Arm Type
Experimental
Arm Description
Health service provision within the first few months of diagnosis which includes physical examination, radiographs, education, exercise, weight loss, assistive devices and pharmacologic therapy.
Intervention Type
Procedure
Intervention Name(s)
Pharmacist-Initiated Intervention in OsteoArthritis (PhIT-OA)
Intervention Description
See Detailed Description.
Primary Outcome Measure Information:
Title
The primary outcome will be the difference in proportion of patients who receive ≥ 5 of the Arthritis Foundation's quality indicators during the six months of the study.
Time Frame
6 months
Title
(Baseline, months 2 and 6 )
Time Frame
Months 2 and 6
Secondary Outcome Measure Information:
Title
There are four secondary outcome measures that will be compared between intervention and usual care subjects at baseline, months 2 and 6:
Time Frame
Months 2 and 6
Title
The difference in change of physical functioning (using the mean score from 17 questions from the WOMAC that are directed towards this construct) between intervention and usual care. This outcome has been used in recent, well-designed trials of OA.
Title
The difference in knee pain (as assessed by five questions on the WOMAC);
Title
The difference in Health Utilities Index Mark 3 (HUI3); and
Title
The direct medical resource utilization using a questionnaire validated for use in musculoskeletal diseases.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age >50 years ≥ 4 weeks of pain, aching or discomfort in or around the knee Overweight or obese defined as BMI defined as ≥ 27 kg/m2 Not actively participating in a formal exercise program within the past 6 months Self-reported difficulty in at least one of the following activities attributed to knee pain: lifting and carrying groceries, walking one quarter of a mile, getting in and out of a chair, or going up and down stairs. Meet eligibility using the criteria on the pharmacist screening form (see attachment) - This form was adapted from the PhIND-OA study and amended to include points #3 to 6 above. Exclusion Criteria: Significant co-morbid disease that would pose a safety threat or impair ability to participate in an exercise program Inability or unwillingness to modify dietary or exercise behaviours. Knee X-Ray within the last 2 years Inability to speak and write English Knee pain due only to referred pain from osteoarthritis of the hip
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carlo Marra, Ph.D
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mary Pack Arthritis Center
City
Vancouver
State/Province
British Columbia
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
22930542
Citation
Marra CA, Cibere J, Grubisic M, Grindrod KA, Gastonguay L, Thomas JM, Embley P, Colley L, Tsuyuki RT, Khan KM, Esdaile JM. Pharmacist-initiated intervention trial in osteoarthritis: a multidisciplinary intervention for knee osteoarthritis. Arthritis Care Res (Hoboken). 2012 Dec;64(12):1837-45. doi: 10.1002/acr.21763.
Results Reference
derived

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Pharmacist-initiated Intervention Trial in OsteoArthritis (PhIT-OA)

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