Quebec Low Back Pain Study: Core Dataset

NCT04791891 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 10000

Last updated 2022-02-11

No results posted yet for this study

Summary

Persistent back pain is the leading cause of years lived with disability worldwide. Current therapeutic interventions are often either not effective or are associated with undesired consequences. These concerns are further amplified by the current opioid epidemic, resulting in an enormous public health crisis. Experts from diverse disciplines including molecular/cellular biology, neuroscience, psychology and public health formed the Quebec Back Pain Consortium to address this challenge. The overall goal of this project is to facilitate research on factors that contribute to the persistence and recovery from back pain. To accomplish this goal, we will recruit individuals suffering from acute and chronic low back pain across the province of Quebec and follow their pain trajectories over two years using an online platform. During that period, satellite projects will investigate specific risk factors including genetics, diet and physical activity, and advanced statistical methods will be used to integrate and interpret the data. A better understanding of factors influencing back pain will eventually allow for improved early intervention, interruption and prevention.

Conditions

  • Low Back Pain

Sponsors & Collaborators

  • Quebec Pain Research Network

    collaborator OTHER
  • Réseau provincial de recherche en adaptation réadaptation

    collaborator UNKNOWN
  • Laval University

    lead OTHER

Principal Investigators

  • Jean-Sebastien Roy, PhD, PT · Laval University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-11-01
Primary Completion
2024-12-31
Completion
2026-12-31

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04791891 on ClinicalTrials.gov