Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-24 @ 9:47 PM
Ignite Modification Date:
2025-12-24 @ 9:47 PM
NCT ID:
NCT04853732
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.
Study:
NCT04853732
Study Brief:
Protocol Section:
NCT04853732