- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05991440
Examining Racial and Socioeconomic Differences in Chronic Low Back Pain (ERASED)
July 9, 2025 updated by: Burel Goodin, Washington University School of Medicine
Racial and Socioeconomic Differences in Chronic Low Back Pain
The purpose of this research study is to gain a better understanding of how people's racial background and socioeconomic status (e.g., income, education, and employment) impact their experiences of chronic low back pain (cLBP).
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
240
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Burel R Goodin, PhD
- Phone Number: 314-273-6403
- Email: burel@wustl.edu
Study Locations
-
-
Missouri
-
St. Louis, Missouri, United States, 63110
- Recruiting
- Washington University School of Medicine
-
Contact:
- Burel R Goodin, PhD
- Phone Number: 314-273-6403
- Email: burel@wustl.edu
-
Principal Investigator:
- Burel R Goodin, PhD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
For this study we will incorporate a combination of clinic-based and community-based participant recruitment.
Participants will be recruited from the Pain Treatment Clinics at the Wash U Pain Center and VUMC, as well as the surrounding communities in St. Louis and Nashville, respectively.
Description
Inclusion:
- Non-specific cLBP that has persisted for at least 3 months and has resulted in pain on at least half the days in the past 6 months.
- Age 18 - 85; the lower end of this age range was chosen to capture the growing prevalence of young adults with cLBP, and participants over 85 years are increasingly likely to meet one or more exclusion criteria.
- Participants report ethnic group as non-Hispanic and racial group as either Black/African American or White/Caucasian.
Exclusion:
- Low back pain that is attributable to other factors such as ankylosing spondylitis, infection, malignancy, compression fracture of other trauma.
- Systemic rheumatic disease/condition (e.g. rheumatoid arthritis, systemic lupus erythematosus, fibromyalgia).
- Any other chronic pain condition that the participant believes to be more prominent or severe than the low back pain.
- A history of clinically significant surgery to the low back within the past year.
- Uncontrolled hypertension (i.e. SBP/DBP of > 150/95), cardiovascular or peripheral arterial disease.
- Poorly controlled diabetes (HbA1c > 8%).
- Neurological disease (e.g. Parkinson's, multiple sclerosis, epilepsy).
- Serious psychiatric disorder requiring hospitalization within the past 12 months or characterized by active suicidal ideation.
- Diminished cognitive function that would interfere with understanding of study procedures.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
To elucidate racial group disparities in clinical symptoms among NHBs and NHWs with cLBP.
Time Frame: two years
|
Clinical pain severity will be observed through quantitative sensory testing and self-reported questionnaires and surveys.
|
two years
|
|
To elucidate racial group disparities in experimental pain sensitivity among NHBs and NHWs with cLBP.
Time Frame: two years
|
Quantitative sensory testing equipment and biological markers assayed via blood samples.
|
two years
|
|
To elucidate racial group disparities in psychosocial risk factors, among NHBs and NHWs with cLBP.
Time Frame: two years
|
Psychosocial risk factors that will be observed will be greater increases in depressive symptoms, anxiety, and perceived stress, as well as greater social isolation and loneliness through the use of self-reported questionnaires and surveys.
|
two years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Burel Goodin, PhD, Washington University School of Medicine
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 22, 2024
Primary Completion (Estimated)
December 31, 2027
Study Completion (Estimated)
December 31, 2028
Study Registration Dates
First Submitted
July 31, 2023
First Submitted That Met QC Criteria
August 7, 2023
First Posted (Actual)
August 14, 2023
Study Record Updates
Last Update Posted (Actual)
July 10, 2025
Last Update Submitted That Met QC Criteria
July 9, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202306132
- R01MD017565 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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