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N/A N=165 Randomized Health Services Research

Long Term Outcomes of Lumbar Epidural Steroid Injections for Spinal Stenosis

Lumbar Spinal Stenosis

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

OutcomeResultp-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

View full record on ClinicalTrials.gov →

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.

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