Clinical Trials Directory

Trials / Recruiting

RecruitingNCT04853732

PRECISION Pain Research Registry

Pain Registry for Epidemiological, Clinical, and Interventional Studies and Innovation

Status
Recruiting
Phase
Study type
Observational
Enrollment
10,000 (estimated)
Sponsor
University of North Texas Health Science Center · Academic / Other
Sex
All
Age
21 Years – 79 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Timeline

Start date
2016-04-01
Primary completion
2030-12-01
Completion
2030-12-01
First posted
2021-04-21
Last updated
2024-01-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04853732. Inclusion in this directory is not an endorsement.