Actively Recruiting
A Multi-Site Feasibility Trial of Embedded Emergency Department Physical Therapy for Low Back Pain
Led by Northwestern University · Updated on 2026-01-06
140
Participants Needed
2
Research Sites
52 weeks
Total Duration
On this page
Sponsors
N
Northwestern University
Lead Sponsor
N
National Center for Complementary and Integrative Health (NCCIH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating a new way of providing physical therapy directly in the emergency department (ED) for adults with low back pain. This multi-site feasibility trial compares this embedded ED physical therapy model to usual care at two hospital EDs within the Northwestern Medicine and University of Utah Health systems. The study aims to test if this approach can be successfully implemented, including enrolling patients and collecting long-term outcome data, as a step toward a larger future trial focused on pain and opioid use outcomes. The trial randomly assigns two hospital EDs to either have a physical therapist available on-site to start timely care for low back pain patients or to continue with usual care, which may include imaging, education, and medications but no ED physical therapist involvement. The intervention period lasts 9 months, followed by 12 months of collecting patient-reported outcomes and electronic health record data. A third hospital ED will contribute baseline data without participating in the intervention or enrollment. Participants are adult patients visiting the ED with low back pain lasting up to 30 days during daytime hours. They will complete surveys over 12 months to measure pain interference and other health outcomes. Researchers will also review health records and survey clinicians to assess how well the intervention is adopted and delivered. The study monitors participant retention and data completeness to inform future research. Overall participation lasts 21 months, including intervention and follow-up phases.
CONDITIONS
Brief Title
A Multi-Site Feasibility Trial of Embedded Emergency Department Physical Therapy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Emergency Department visit with primary diagnosis related to low back pain
- ED visit occurring at an ED site participating in randomization (Northwestern Memorial Hospital, University of Utah Hospital)
- ED visit check-in time during the hours of 8am-8pm
- Current episode of low back pain less than or equal to 30 days, defined as pain between the 12th rib and buttocks
- Age greater than or equal to 18 years; there is no age maximum
- English or Spanish-speaking
You will not qualify if you...
- "Red flag" symptoms indicating a life or limb-threatening process
- Currently in police custody
- Unable to consent
- Known pregnancy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) during the emergency department visit hours of 8am-8pm
Duration - 9 months
Participants receive either embedded emergency department physical therapy initiated during their emergency department visit or usual care treatment for low back pain, which may include imaging, education, and/or medication as per the treating physician's usual practice.
Visits occur as part of routine emergency department care; additional participant surveys and assessments are collected longitudinally
Duration - 12 months
Participants complete longitudinal surveys and have their health outcomes tracked for up to 12 months following the treatment period to assess effectiveness and healthcare use.
Periodic survey assessments and electronic health record data collection over 12 months
Trial Site Locations
Total: 2 locations
1
Northwestern Memorial Hospital
Chicago, Illinois, United States, 60611
Actively Recruiting
2
University of Utah
Salt Lake City, Utah, United States, 84112
Actively Recruiting
Research Team
H
Howard Kim, MD, MS
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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