Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
80 participants
INTERVENTIONAL
2005-07-31
2010-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Physician telephone consultation
Received direct telephone consultation with pain physician about index patient
Physician telephone consultation
Pain physician support for family physician treating patient
Usual family physician care
Usual family physician care (without direct telephone consultation with pain physician)
Usual family physician care
Usual family physician care without telephone consultation with pain physician
Interventions
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Physician telephone consultation
Pain physician support for family physician treating patient
Usual family physician care
Usual family physician care without telephone consultation with pain physician
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University of Calgary
OTHER
Responsible Party
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Dr. Sue Ross
Adjunct Professor
Principal Investigators
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Neil Drummond, PhD
Role: STUDY_DIRECTOR
University of Calgary
Locations
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Alberta Health Services Chronic Pain Centre
Calgary, Alberta, Canada
Countries
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Other Identifiers
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Project ID 18618
Identifier Type: -
Identifier Source: org_study_id