Actively Recruiting

Phase 2
Age: 18Years +
All Genders
Healthy Volunteers
ID05452876

Alberta Back Care Pathway (ABCp) for Low Back Pain Management Using Guideline-Based Interventions in Primary Care

Led by University of Alberta · Updated on 2025-08-29

240

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of Alberta

Lead Sponsor

C

Canadian Chiropractic Research Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

Low back pain (LBP) causes increasing pain, disability, addiction, and healthcare costs, especially in Alberta where family physicians face barriers in providing effective, guideline-based care. These barriers include lack of training, limited low-cost access to treatments, and insufficient time and reimbursement. The Alberta Back Care Pathway (ABCp) was developed with input from patients, providers, and scientists to offer family physicians a common, guideline-based approach to assess and manage LBP patients effectively in daily practice. The ABCp trains physicians to categorize patients into five groups, each with evidence-based interventions that can be offered at no or low cost to patients and minimal cost to the healthcare system. The study compares the ABCp intervention to usual care in a multi-clinic, controlled, non-randomized stepped-wedge design. The intervention includes patient education, structured exercise programs, and decision-making tools to reduce low-value care. Enrollment lasts one year, followed by a one-year follow-up, with training provided for clinicians and possible telehealth delivery of the GLA:D Back program. Participants will be assessed using ABCp categories and followed for healthcare resource use, quality of life, and opioid use. Data collected include the number of visits to family physicians, specialist referrals, and imaging requests over about 30 months. Quality of life is measured with patient-reported outcomes, and opioid prescription data are tracked. The study aims to reduce healthcare costs and improve outcomes through guideline-based care, with a total project duration of about 2.5 years including pre-implementation activities, enrollment, and follow-up.

CONDITIONS

Brief Title

Alberta Back Care Pathway (ABCp)

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Licensed physicians in the Edmonton West Primary Care Network (EWPCN) and the Calgary Chronic Pain Centre (CPC)
  • Age 18 years or older with no upper age limit
  • English speaking and resident of Alberta with ability to understand information and provide consent
  • Patients categorized by physicians using ABCp into Acute, SubAcute, Chronic, Chronic Non-Responsive or Radiculopathy groups
  • For CPC site: patients must have depression and anxiety screening scores below specified thresholds
Not Eligible

You will not qualify if you...

  • Low back pain caused by a recent motor vehicle accident
  • Workers' Compensation Board (WCB) cases
  • Known contraindications to exercise (e.g., unstable angina, uncontrolled arrhythmia, severe aortic stenosis)
  • Current participation in supervised exercise or rehabilitation programs or enrollment in another interventional clinical trial
  • Plans for or undergoing spine surgery or procedures that contraindicate study interventions

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Up to 12 months

Participants receive care based on the Alberta Back Care Pathway (ABCp) which includes categorization of low back pain and delivery of guideline-based interventions such as education, therapeutic exercise, reassurance, manual therapy, and non-opioid medications, either in-person or via telehealth.

Visits scheduled according to treatment needs and clinical categorization

Follow-up

Duration - 12 months

Participants are followed for an additional 12 months after treatment to monitor healthcare resource utilization, quality of life, opioid use, and other outcomes.

Periodic assessments during follow-up period

Trial Site Locations

Total: 1 location

1

University of Alberta

Edmonton, Alberta, Canada, T6G 2G4

Actively Recruiting

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Research Team

J

Jennifer N Glumpak, MScPT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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