Active — Not RecruitingNot Applicable

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

United States1,800 participantsStarted 2023-03-14

Plain-language 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).

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. aged 18 years and older
✓. initiating an outpatient visit for LBP at a participating PCP clinic
✓. agree to participate and complete baseline questionnaire (in lieu of formal written documentation of consent)

Exclusion criteria

✕. inability to provide consent or complete outcome questionnaires
✕. positive screening for cauda equina symptoms (loss of total control of bowel/bladder associated with this episode of LBP )

What they're measuring

Change in Pain Interference as measured by PROMIS (Patient-Reported Outcomes Measurement Information System)

Timeframe: Baseline, 3 Months

Change in Physical Function as measured by PROMIS (Patient-Reported Outcomes Measurement Information System)

Timeframe: Baseline, 3 Months

Trial details

NCT IDNCT05626049

SponsorDuke University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-10-17

View on ClinicalTrials.gov More Pain, Back trials