Trial of Inserting Prevalence Information Into Lumbar Spine Imaging Reports (LIRE)
Primary Purpose
Low Back Pain, Back Pain, Lumbar Pain
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Epidemiologic benchmarks included in lumbar imaging reports
Sponsored by
About this trial
This is an interventional health services research trial for Low Back Pain focused on measuring pragmatic trial, stepped-wedge design, cluster-randomized trial
Eligibility Criteria
Inclusion Criteria:
- Imaging of lumbar spine requested by primary care provider
Exclusion Criteria:
- Age < 18years
Sites / Locations
- Kaiser Permanente of Northern California
- Henry Ford Health System
- Mayo Clinic Health Systems
- Group Health Cooperative
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Intervention Arm
Usual Care Arm
Arm Description
Epidemiologic benchmarks included in lumbar imaging reports
Clinics with typical lumbar imaging reports (no epidemiologic benchmarks included)
Outcomes
Primary Outcome Measures
Relative Value Unit (RVU) for Spine-related Interventions
Spine-related RVUs are a composite measure of back pain interventions that combine the overall intensity of resource utilization for back pain care in a single metric. Each spine-related procedure has an RVU associated with it representing the relative cost of the work and practice components of the procedure. The outcome measure includes the sum of the RVUs of inpatient and outpatient procedures in the year following index imaging. The Medicare conversion factor during the study period was approximately $35/RVU.
Secondary Outcome Measures
Number of Participants With Opioid Prescription Within 12 Months of Index Imaging
An indicator of one or more opioid prescriptions from a LIRE provider (a provider who ordered index imaging for one or more participants in the LIRE Trial) within 12 months of index imaging as reported in the health system medical record.
Number of Participants With Opioid Prescription Within 90 Days of Index Imaging
An indicator of one or more opioid prescriptions from a LIRE provider (a provider who ordered index imaging for one or more participants in the LIRE Trial) within 90 days of index imaging as reported in the health system medical record.
Number of Participants With an Opioid Prescription Within 30 Days of Index Imaging
An indicator of one or more opioid prescriptions from a LIRE provider (a provider who ordered index imaging for one or more participants in the LIRE Trial) within 30 days of index imaging as reported in the health system medical record.
Number of Participants With Cross-sectional Imaging Within 12 Months of Plain Film Index Imaging
An indicator of one or more instances of cross-sectional imaging (MRI or CT) within 12 months of plain film index imaging. Participants with cross-sectional index imaging are excluded.
Number of Participants With Cross-sectional Imaging Within 90 Days of Plain Film Index Imaging
An indicator of one or more instances of cross-sectional imaging (MRI or CT) within 90 days of plain film index imaging. Participants with cross-sectional index imaging are excluded.
Back-pain Related Estimated Payer Costs
Payer costs were not evaluated due to funding constraints.
Number of Participants With Spine Surgery Within 18 Month of Index Imaging
An indicator or one or more spine surgeries within 18 months of index imaging. Spine surgery includes decompression surgery, spinal fusion or proxies for spine fusion, or other surgeries involving the lumbar, sacral, or thoracic spine.
Relative Value Unit (RVU) for Spine-related Interventions at 24 Months
24-month outcomes were not evaluated due to funding constraints
Opioid Prescriptions at 24 Months
24-month outcomes were not evaluated due to funding constraints
Cross-sectional Imaging at 24 Months
24-month outcomes were not evaluated due to funding constraints
Back-pain Related Estimated Payer Costs at 24 Months
24-month outcomes were not evaluated due to funding constraints
Spine- Related Surgical Interventions
24-month outcomes were not evaluated due to funding constraints
Full Information
NCT ID
NCT02015455
First Posted
December 6, 2013
Last Updated
January 20, 2022
Sponsor
University of Washington
Collaborators
Mayo Clinic, Henry Ford Health System, Kaiser Permanente, Oregon Health and Science University, National Institutes of Health (NIH), National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), National Center for Complementary and Integrative Health (NCCIH)
1. Study Identification
Unique Protocol Identification Number
NCT02015455
Brief Title
Trial of Inserting Prevalence Information Into Lumbar Spine Imaging Reports
Acronym
LIRE
Official Title
Lumbar Imaging With Reporting of Epidemiology: A Pragmatic Cluster Randomized Trial
Study Type
Interventional
2. Study Status
Record Verification Date
January 2022
Overall Recruitment Status
Completed
Study Start Date
October 1, 2013 (Actual)
Primary Completion Date
December 14, 2018 (Actual)
Study Completion Date
December 14, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
Mayo Clinic, Henry Ford Health System, Kaiser Permanente, Oregon Health and Science University, National Institutes of Health (NIH), National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), National Center for Complementary and Integrative Health (NCCIH)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The overall goal of the Lumbar Image Reporting with Epidemiology (LIRE) is to perform a large, pragmatic, cluster randomized controlled trial to determine the effectiveness of a simple, inexpensive and easy to deploy intervention - insertion of epidemiological benchmarks into lumbar spine imaging reports - at reducing subsequent tests and treatments. The investigator's main hypothesis is that for patients referred from primary care providers, inserting epidemiological evidence in lumbar spine imaging reports will reduce subsequent diagnostic and therapeutic interventions, including cross-sectional imaging (MR/CT), opioid prescriptions, spinal injections and surgery.
Detailed Description
The long-term public health significance is that a simple, inexpensive intervention has the potential to substantially reduce unnecessary and expensive care for back pain patients. Importantly, this approach could be applied to a wide range of other conditions and other diagnostic tests (e.g. other imaging tests, laboratory tests, genetic testing). If this study is positive, adding epidemiologic benchmarks to diagnostic test reporting could become the dominant paradigm for communicating all diagnostic information.
To test this hypothesis, the investigators propose to conduct a pragmatic cluster, randomized controlled trial, randomly assigning primary care clinics at four large health systems to receive either standard lumbar spine imaging reports or reports containing epidemiological benchmarks for common imaging findings. The investigators will use a novel stepped wedge randomization scheme that temporally randomizes sites, allowing within-site before/after comparisons in addition to between-site comparisons, while assuring that all sites will eventually receive the intervention. The primary outcome will be a metric of back-related intervention intensity. The primary analysis will occur at the clinic level and not the patient level.
This pragmatic trial will demonstrate both the feasibility of randomly assigning clinics within large health systems as well as the feasibility of passively collecting outcomes data up to two years after enrollment using the robust electronic medical records systems available at each health system.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Back Pain, Back Pain, Lumbar Pain, Backache
Keywords
pragmatic trial, stepped-wedge design, cluster-randomized trial
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
250401 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intervention Arm
Arm Type
Experimental
Arm Description
Epidemiologic benchmarks included in lumbar imaging reports
Arm Title
Usual Care Arm
Arm Type
No Intervention
Arm Description
Clinics with typical lumbar imaging reports (no epidemiologic benchmarks included)
Intervention Type
Other
Intervention Name(s)
Epidemiologic benchmarks included in lumbar imaging reports
Intervention Description
Epidemiologic benchmarks inserted into lumbar imaging reports
Primary Outcome Measure Information:
Title
Relative Value Unit (RVU) for Spine-related Interventions
Description
Spine-related RVUs are a composite measure of back pain interventions that combine the overall intensity of resource utilization for back pain care in a single metric. Each spine-related procedure has an RVU associated with it representing the relative cost of the work and practice components of the procedure. The outcome measure includes the sum of the RVUs of inpatient and outpatient procedures in the year following index imaging. The Medicare conversion factor during the study period was approximately $35/RVU.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Number of Participants With Opioid Prescription Within 12 Months of Index Imaging
Description
An indicator of one or more opioid prescriptions from a LIRE provider (a provider who ordered index imaging for one or more participants in the LIRE Trial) within 12 months of index imaging as reported in the health system medical record.
Time Frame
12 months
Title
Number of Participants With Opioid Prescription Within 90 Days of Index Imaging
Description
An indicator of one or more opioid prescriptions from a LIRE provider (a provider who ordered index imaging for one or more participants in the LIRE Trial) within 90 days of index imaging as reported in the health system medical record.
Time Frame
90 days
Title
Number of Participants With an Opioid Prescription Within 30 Days of Index Imaging
Description
An indicator of one or more opioid prescriptions from a LIRE provider (a provider who ordered index imaging for one or more participants in the LIRE Trial) within 30 days of index imaging as reported in the health system medical record.
Time Frame
30 days
Title
Number of Participants With Cross-sectional Imaging Within 12 Months of Plain Film Index Imaging
Description
An indicator of one or more instances of cross-sectional imaging (MRI or CT) within 12 months of plain film index imaging. Participants with cross-sectional index imaging are excluded.
Time Frame
12 months
Title
Number of Participants With Cross-sectional Imaging Within 90 Days of Plain Film Index Imaging
Description
An indicator of one or more instances of cross-sectional imaging (MRI or CT) within 90 days of plain film index imaging. Participants with cross-sectional index imaging are excluded.
Time Frame
90 days
Title
Back-pain Related Estimated Payer Costs
Description
Payer costs were not evaluated due to funding constraints.
Time Frame
12 months
Title
Number of Participants With Spine Surgery Within 18 Month of Index Imaging
Description
An indicator or one or more spine surgeries within 18 months of index imaging. Spine surgery includes decompression surgery, spinal fusion or proxies for spine fusion, or other surgeries involving the lumbar, sacral, or thoracic spine.
Time Frame
18 months
Title
Relative Value Unit (RVU) for Spine-related Interventions at 24 Months
Description
24-month outcomes were not evaluated due to funding constraints
Time Frame
24 months
Title
Opioid Prescriptions at 24 Months
Description
24-month outcomes were not evaluated due to funding constraints
Time Frame
24 months
Title
Cross-sectional Imaging at 24 Months
Description
24-month outcomes were not evaluated due to funding constraints
Time Frame
24 months
Title
Back-pain Related Estimated Payer Costs at 24 Months
Description
24-month outcomes were not evaluated due to funding constraints
Time Frame
24 months
Title
Spine- Related Surgical Interventions
Description
24-month outcomes were not evaluated due to funding constraints
Time Frame
24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Imaging of lumbar spine requested by primary care provider
Exclusion Criteria:
Age < 18years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey G Jarvik, MD, MPH
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kaiser Permanente of Northern California
City
Oakland
State/Province
California
Country
United States
Facility Name
Henry Ford Health System
City
Detroit
State/Province
Michigan
Country
United States
Facility Name
Mayo Clinic Health Systems
City
Minneapolis
State/Province
Minnesota
Country
United States
Facility Name
Group Health Cooperative
City
Seattle
State/Province
Washington
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
26493088
Citation
Jarvik JG, Comstock BA, James KT, Avins AL, Bresnahan BW, Deyo RA, Luetmer PH, Friedly JL, Meier EN, Cherkin DC, Gold LS, Rundell SD, Halabi SS, Kallmes DF, Tan KW, Turner JA, Kessler LG, Lavallee DC, Stephens KA, Heagerty PJ. Lumbar Imaging With Reporting Of Epidemiology (LIRE)--Protocol for a pragmatic cluster randomized trial. Contemp Clin Trials. 2015 Nov;45(Pt B):157-163. doi: 10.1016/j.cct.2015.10.003. Epub 2015 Oct 19.
Results Reference
result
PubMed Identifier
32886121
Citation
Jarvik JG, Meier EN, James KT, Gold LS, Tan KW, Kessler LG, Suri P, Kallmes DF, Cherkin DC, Deyo RA, Sherman KJ, Halabi SS, Comstock BA, Luetmer PH, Avins AL, Rundell SD, Griffith B, Friedly JL, Lavallee DC, Stephens KA, Turner JA, Bresnahan BW, Heagerty PJ. The Effect of Including Benchmark Prevalence Data of Common Imaging Findings in Spine Image Reports on Health Care Utilization Among Adults Undergoing Spine Imaging: A Stepped-Wedge Randomized Clinical Trial. JAMA Netw Open. 2020 Sep 1;3(9):e2015713. doi: 10.1001/jamanetworkopen.2020.15713.
Results Reference
result
PubMed Identifier
34535520
Citation
Gold LS, Marcum ZA, Meier EN, Turner JA, James KT, Kallmes DF, Luetmer PH, Griffith B, Sherman KJ, Friedly JL, Suri P, Deyo RA, Johnston SK, Avins AL, Heagerty PJ, Jarvik JG. Patient, Provider, and Clinic Characteristics Associated with Opioid and Non-Opioid Pain Prescriptions for Patients Receiving Low Back Imaging in Primary Care. J Am Board Fam Med. 2021 Sep-Oct;34(5):950-963. doi: 10.3122/jabfm.2021.05.210033.
Results Reference
derived
PubMed Identifier
33595635
Citation
Suri P, Meier EN, Gold LS, Marcum ZA, Johnston SK, James KT, Bresnahan BW, O'Reilly M, Turner JA, Kallmes DF, Sherman KJ, Deyo RA, Luetmer PH, Avins AL, Griffith B, Heagerty PJ, Rundell SD, Jarvik JG, Friedly JL. Providing Epidemiological Data in Lumbar Spine Imaging Reports Did Not Affect Subsequent Utilization of Spine Procedures: Secondary Outcomes from a Stepped-Wedge Randomized Controlled Trial. Pain Med. 2021 Jun 4;22(6):1272-1280. doi: 10.1093/pm/pnab065.
Results Reference
derived
PubMed Identifier
33559061
Citation
Marcum ZA, Gold LS, James KT, Meier EN, Turner JA, Kallmes DF, Cherkin DC, Deyo RA, Sherman KJ, Luetmer PH, Avins AL, Griffith B, Friedly JL, Suri P, Heagerty PJ, Jarvik JG. Effects of Including Epidemiologic Data in Lumbar Spine Imaging Reports on Prescribing Non-Opioid Medications for Pain. J Gen Intern Med. 2021 Aug;36(8):2237-2243. doi: 10.1007/s11606-021-06627-6. Epub 2021 Feb 8.
Results Reference
derived
PubMed Identifier
26772801
Citation
Johnson KE, Neta G, Dember LM, Coronado GD, Suls J, Chambers DA, Rundell S, Smith DH, Liu B, Taplin S, Stoney CM, Farrell MM, Glasgow RE. Use of PRECIS ratings in the National Institutes of Health (NIH) Health Care Systems Research Collaboratory. Trials. 2016 Jan 16;17:32. doi: 10.1186/s13063-016-1158-y.
Results Reference
derived
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Trial of Inserting Prevalence Information Into Lumbar Spine Imaging Reports
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