Clinical trial Recruiting at 1 site Observational Ages 21 to 79

Registry for chronic low back pain and healthy controls

Official title: Pain Registry for Epidemiological, Clinical, and Interventional Studies and Innovation

Run by University of North Texas Health Science Center · NCT04853732 · Data updated 2026-11-12

This study is trying to learn more about chronic low back pain by comparing people who have it with those who don’t, to see how pain affects their lives and what treatments work best.

Quick facts

Study typeObservational
Ages21 Years to 79 Years
SexAll
Enrollment10000 (estimated)
SponsorUniversity of North Texas Health Science Center
Academic / other
Locations1 site (Fort Worth, Texas)
StatusRecruiting
StartedApril 2016
Main results expectedDecember 2030
Study endsDecember 2030
Registry record updatedJanuary 16, 2024
Trial IDNCT04853732 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include individuals residing in the contiguous 48 United States or District of Columbia with chronic low back pain or healthy volunteers without chronic pain.

Probably not a fit

Patients who are pregnant or residing in institutional facilities may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The PRECISION Pain Research Registry enrolls individuals with chronic low back pain and those without chronic pain to investigate the epidemiology and management of chronic pain. Participants complete various validated questionnaires at scheduled encounters to gather comprehensive data on their pain experiences and treatment approaches. The registry also collects biological specimens for future research on potential biomarkers related to chronic pain. This observational study aims to enhance understanding and improve management strategies for chronic low back pain.

Why it matters

Potential benefit: If successful, this registry could lead to improved treatment options and management strategies for individuals suffering from chronic low back pain.

How similar studies have gone: Other studies have shown success in utilizing similar observational approaches to understand chronic pain, making this registry a valuable addition to existing research.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Must reside within the contiguous 48 United States or District of Columbia
* Must provide a valid, government-issued identification with photo and birthdate
* Must have Internet access or telephone service to communicate with registry staff
* Must have sufficient English language proficiency to complete case report forms independently or with assistance from registry staff
* Must have a primary care physician or other physician who regularly provides health care
* Must provide the name, dose, and frequency of use of all current medications
* Case participants must have chronic low back pain
* Control participants must be free of any chronic pain and may include healthy volunteers

Exclusion Criteria:

* Must not be pregnant
* Must not reside in an institutional facility

Where it's running

  • University of North Texas Health Science Center
    Fort Worth, Texas, United States
    Recruiting

Study contacts

  • Principal investigator: John C Licciardone, DO, MS, MBA — University of North Texas Health Science Center
  • Study coordinator: Cathleen Kearns, BA
  • Email: orcstudyoperations@unthsc.edu
  • Phone: 817-735-0515

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.