Implementation of the ACP Guideline for Low Back Pain (IMPACt-LBP)

Last updated: November 18, 2025
Sponsor: Duke University
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Chronic Pain

Pain

Treatment

Usual Care

Primary Spine Provider Model

Clinical Study ID

NCT05626049
Pro00109780
  • Ages > 18
  • All Genders

Study Summary

The purpose of this study is to assess whether the primary spine practitioner (PSP) model of care will lead to improvements in patient outcomes, as compared to usual care, based on change in patient-reported PROMIS Pain Interference and Physical Function from baseline to 3 months in patients aged 18 years and older with a primary complaint of low back pain (LBP).

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. aged 18 years and older

  2. initiating an outpatient visit for LBP at a participating PCP clinic

  3. agree to participate and complete baseline questionnaire (in lieu of formal writtendocumentation of consent)

Exclusion

Exclusion Criteria:

  1. inability to provide consent or complete outcome questionnaires

  2. positive screening for cauda equina symptoms (loss of total control of bowel/bladderassociated with this episode of LBP )

Study Design

Total Participants: 1800
Treatment Group(s): 2
Primary Treatment: Usual Care
Phase:
Study Start date:
March 14, 2023
Estimated Completion Date:
June 30, 2026

Study Description

This study is a pragmatic, multi-site, two-arm cluster-randomized trial with the unit of randomization at the primary care clinic level. The overall goal is to evaluate implementation of the American College of Physicians (ACP) guideline for LBP by assessing the comparative effectiveness of the PSP model, which involves first contact care for LBP patients from either a physical therapist (PT) or a doctor of chiropractic (DC), versus usual care, which involves first contact care with primary care physicians. The study includes patients aged 18 years and older with a chief complaint of LBP.

Co-primary endpoints to be assessed are changes in Patient- Reported Outcomes Measurement Information System (PROMIS) Pain Interference and Physical Function from baseline to 3 months. The Investigators have chosen to use these co-primary endpoints as they represent two domains that are important factors related to patient improvement.

Secondary endpoints collected at baseline, 3, 6 and 12 months include Pain Catastrophizing Scale - 4-item short form, PROMIS Global-10 (v1.2), opioid use, imaging and diagnostic testing, provider visits, and LBP-associated procedures and treatments: surgical procedures, medication prescriptions, hospital admissions and emergency room visits.

Additional exploratory analyses among enrolled patients will assess whether the PSP model leads to 1) long-term improvement compared to usual care using the PROMIS Pain Interference and Physical Function at 6, 12, and 24 months; and 2) lower healthcare utilization and costs for LBP at 12 and 24 months.

Patients enrolled within the first 12 months of the data collection phase will be included in the 24-month exploratory analyses. Additional analyses will evaluate LBP-related utilization within the academic healthcare systems among all patients seen in intervention versus control primary care clinics utilizing de-identified clinic level data extracted from the EHR.

A total of approximately 1,800 patients who seek care at a participating primary care clinic with a complaint of LBP and meet study eligibility criteria will be enrolled.

Connect with a study center

  • University of Iowa

    Iowa City, Iowa 52242
    United States

    Site Not Available

  • University of Iowa

    Iowa City 4862034, Iowa 4862182 52242
    United States

    Site Not Available

  • Dartmouth Health

    Lebanon, New Hampshire 03755
    United States

    Site Not Available

  • Dartmouth Health

    Lebanon 5088597, New Hampshire 5090174 03755
    United States

    Site Not Available

  • Duke Health

    Durham, North Carolina 27713
    United States

    Site Not Available

  • Duke Health

    Durham 4464368, North Carolina 4482348 27713
    United States

    Site Not Available

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