N/A
N=165
Long Term Outcomes of Lumbar Epidural Steroid Injections for Spinal Stenosis
Lumbar Spinal Stenosis
Bottom Line
View on ClinicalTrials.gov: NCT02260401 ↗Enrolled (actual)
165
Serious AEs
0.0%
Results posted
Jun 2017
Primary outcome: Primary: Utilization of ESI — 3.6; 3.3 number of ESI between 18-24 months
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Individualized report (Other)
- Age
- Adult, Older Adult · 50+ yrs
- Sex
- All
- Sponsor
- University of Washington
- Primary completion
- Jul 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Utilization of ESI |
3.6; 3.3 | — |
| SECONDARY Healthcare Utilization |
— | — |
Summary
Spinal stenosis is one of the most common causes of low back pain among older adults and can result in significant disability. Despite this, it still isn't known which treatments are most effective or what outcomes are most important to these older adults. Through a Patient Centered Outcomes Research Institute (PCORI) contract, the investigators are building on the existing infrastructure of an AHRQ-funded (ARRA CHOICE award) comparative effectiveness research (CER) trial of epidural steroid injections (ESI) for spinal stenosis (the LESS trial) to address several critical research questions. The proposed study will answer the following key questions. Do decision aids tailored to older adults with spinal stenosis change patient decision-making regarding subsequent treatments? Do patients respond differently at subsequent outcome assessments time-points after receiving tailored decision aids that contain their own individual outcome data from prior treatments? The investigators hypothesize that providing these individualized reports will allow patients to make more informed choices regarding subsequent treatments, leading to reduced use of ineffective treatments and improved outcomes overall.
Eligibility Criteria
Inclusion Criteria
Patients already enrolled in the LESS trial will be eligible for participation in the LESSER trial
Exclusion Criteria
none
Data sourced from ClinicalTrials.gov (NCT02260401). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.