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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01923324
Other study ID # Project ID 18618
Secondary ID
Status Completed
Phase N/A
First received August 13, 2013
Last updated August 13, 2013
Start date July 2005
Est. completion date December 2010

Study information

Verified date August 2013
Source University of Calgary
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate whether pain control for patients with chronic pain is improved by the availability of structured telephone consultations between the patients' family physicians and pain physicians, compared to pain control for patients receiving usual care.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date December 2010
Est. primary completion date December 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients referred to Alberta Health Services chronic pain center in Calgary with neurological or muscular skeletal pain

Exclusion Criteria:

- increased risk for suicide, very complex patients, family physician could not reliably identify patient's pain problem, or condition warranted expedited consultation with pain physician, case represented a new presentation of chronic regional pain syndrome, or low back pain with radicular symptoms or sciatica

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
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

Locations

Country Name City State
Canada Alberta Health Services Chronic Pain Centre Calgary Alberta

Sponsors (1)

Lead Sponsor Collaborator
University of Calgary

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Pain treatment satisfaction scale (patient) 6 months No
Other Family physician satisfaction questionnaire 6 months No
Other Family physician knowledge transfer questionnaire 6 months No
Primary Numerical Rating Scale for pain intensity (NRS) 11 point scale (from zero to 10), zero equals no pain, 10 worst possible pain. 6 months No
Secondary Pain Disability Index (PDI) 7 item self-report scale assessing pain disability 6 months No
Secondary Patient Global Impression of Change Scale (PGIC) 7 point scale 6 months No
Secondary Short Form Health Survey (SF-36) Generic quality of life scale. 6 months No
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