- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01923324
Standard Telephone Consultation for Pain (STC)
August 13, 2013 updated by: Dr. Sue Ross, University of Calgary
Physician to Physician Telephone Consultation for Chronic Pain Patients: a Pragmatic Randomized Trial
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
80
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
-
-
Alberta
-
Calgary, Alberta, Canada, T2S 3C3
- Alberta Health Services Chronic Pain Centre
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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 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: Physician telephone consultation
Received direct telephone consultation with pain physician about index patient
|
Pain physician support for family physician treating patient
|
|
Active Comparator: Usual family physician care
Usual family physician care (without direct telephone consultation with pain physician)
|
Usual family physician care without telephone consultation with pain physician
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numerical Rating Scale for pain intensity (NRS)
Time Frame: 6 months
|
11 point scale (from zero to 10), zero equals no pain, 10 worst possible pain.
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Disability Index (PDI)
Time Frame: 6 months
|
7 item self-report scale assessing pain disability
|
6 months
|
|
Patient Global Impression of Change Scale (PGIC)
Time Frame: 6 months
|
7 point scale
|
6 months
|
|
Short Form Health Survey (SF-36)
Time Frame: 6 months
|
Generic quality of life scale.
|
6 months
|
Other Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Pain treatment satisfaction scale (patient)
Time Frame: 6 months
|
6 months
|
|
Family physician satisfaction questionnaire
Time Frame: 6 months
|
6 months
|
|
Family physician knowledge transfer questionnaire
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Neil Drummond, PhD, University of Calgary
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
July 1, 2005
Primary Completion (Actual)
December 1, 2010
Study Completion (Actual)
December 1, 2010
Study Registration Dates
First Submitted
August 13, 2013
First Submitted That Met QC Criteria
August 13, 2013
First Posted (Estimate)
August 15, 2013
Study Record Updates
Last Update Posted (Estimate)
August 15, 2013
Last Update Submitted That Met QC Criteria
August 13, 2013
Last Verified
August 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Project ID 18618
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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