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Biopsychosocial Exploration of Pain Profiles in Inflammatory and Chronic Non-specific Axial Low Back Pain

NCT02704845 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 58

Last updated 2016-10-21

No results posted yet for this study

Summary

The biopsychosocial model is well established in chronic low back pain (CLBP) research. Nevertheless, researchers to date have overlooked the biopsychosocial aspects of Inflammatory Low Back pain (ILBP). Most health care providers are biologically oriented in their treatment of ILBP, neglecting its possible multidimensional nature. It is true that people with ILBP may present with more complex pain and physical limitations than those with chronic non-specific low back pain (CNSLBP), but it remains unexplored whether or not these limitations are affected by the same pain factors that affect CNSLBP patients. This study aims to explore and compare the biopsychosocial back pain profiles of adults with ILBP and CNSLBP.

Conditions

  • Back Pain
  • Spondylitis, Ankylosing
  • Low Back Pain

Sponsors & Collaborators

  • University of Dublin, Trinity College

    lead OTHER

Principal Investigators

  • Fiona Wilson · Trinity College Dublin, Ireland

  • Lolwah A Al-Rashed · Trinity College Dublin, Ireland

  • Finbar O'Shea · St. James's Hospital, Dublin, Ireland

  • Deborah Falla · University Medical Center Göttingen, Georg-August University, Göttingen, Germany

  • Marco Barbero · University of Applied Sciences and Arts of Southern Switzerland (SUPSI), Manno, Switzerland

  • Aisling Brenan · Adelaide and Meath Hospital Dublin incorporating the National Children's Hospital (Tallaght Hospital), Dublin, Ireland

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-09-30
Primary Completion
2016-08-31
Completion
2016-08-31

Countries

  • Ireland

Study Locations

More Related Trials

Entities

Diseases

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 NCT02704845 on ClinicalTrials.gov