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

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.

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.

Clinical Trials on Chronic Pain

Clinical Trials on Physician telephone consultation

Subscribe