PRECISION Pain Research Registry

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

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT04853732

Acronym

PRECISION

Enrollment

10000

Registered

2021-04-21

Start date

2016-04-30

Completion date

2030-12-31

Last updated

2024-01-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Low Back Pain

Brief 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.

Interventions

None listed

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

21 Years to 79 Years

Healthy volunteers

Yes

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

Design outcomes

Primary

Measure	Time frame	Description
Case-Control Status	Upon registry enrollment	Chronic Low Back Pain Case or Chronic Pain-Free Control

Countries

United States

Contacts

Primary ContactCathleen Kearns, BA

orcstudyoperations@unthsc.edu817-735-0515

Backup ContactSamantha Johnson, BS

orcstudyoperations@unthsc.edu817-735-5410

Outcome results