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PRECISION Pain Research Registry — PRECISION  

Chronic Low Back Pain Clinical Trial

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

Clinical Trial Summary

The PRECISION Pain Research Registry enrolls participants with chronic low back pain (cases) and participants who are free of chronic pain (controls) to study the epidemiology and management of chronic pain. The vision of the registry is to conduct research to provide a future for all unbounded by pain.

Clinical Trial Description

Case participants complete case report forms at quarterly encounters, whereas control participants complete a case report form only at an initial encounter. A series of validated or recommended research instruments are used or adapted by the registry for deployment in its case report forms. These may include some or all of the following at a given encounter: - National Institutes of Health Minimum Dataset for Research on Chronic Low Back Pain - Roland-Morris Disability Questionnaire - Patient-Reported Outcomes Measurement Information System (PROMIS-29) - History of Medical Conditions Inventory - Pain Sensitivity Questionnaire - Pain Catastrophizing Scale - Pain Self-Efficacy Questionnaire - Non-Pharmacological Treatments Inventory - Pharmacological Treatments Summary - Drug Adverse Events Index - Physician Profile - Physician Communication Behavior Questionnaire - Physician Consultation and Relational Empathy Measure - Patient Satisfaction Questionnaire (PSQ-18) These instruments include measures that may serve as the independent or dependent variables in various substudies conducted by the registry over time, including observational studies (e.g., case-control studies, cohort studies) and randomized controlled trials. The registry also maintains a biobank of biological specimens that have been collected from enrolled participants, including saliva and blood that may be used for DNA sequencing or biomarker analysis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04853732
Study type Observational [Patient Registry]
Source University of North Texas Health Science Center
Contact Cathleen Kearns, BA
Phone 817-735-0515
Email orcstudyoperations@unthsc.edu
Status Recruiting
Phase
Start date April 2016
Completion date December 2030
View Details
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