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Prognostic Factor Research of Sensory Profiles in Development of Central Sensitization

V

Vrije Universiteit Brussel

Status

Completed

Conditions

Sensory Profiles
Nociplastic Pain
Low Back Pain
Central Sensitisation

Treatments

Other: In line with the Dutch guideline for non-specific low back pain, Standard usual care for non-specific low back pain was applied.

Study type

Observational

Funder types

Other

Identifiers

NCT04974229
ProgCohSt-M15.169564

Details and patient eligibility

About

A longitudinal observational cohort study to investigate the value of prognostic factors, here sensory profiles , and others, in the development of central sensitization in the low back pain population. A type 2 prognostic factor research following the PROGRESS framework. Sensory profiles are identified a prognostic factors which can predict the development of central sensitization in the low back pain population.

Full description

After performing an univariable linear regression analyses the regression model predicts the dependent variable, central sensitization, significantly, and the models are significant prediction factors of the development of central sensitization. In unadjusted analyses, all four sensory profiles were significantly associated with the development of central sensitization (P<0.001).

After adjusting for pain, disability, age, and duration of low back pain, baseline sensory profiles remained significant predictors of central sensitization. On the other hand, all other predictor variables did not contribute to the prediction of central sensitization.

Enrollment

102 patients

Sex

All

Ages

18 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • acute low back pain (< 6 weeks)
  • with or without radiating pain
  • aged 18 to 60 years
  • a pain-free episode for at least 3 months before the onset of their current back pain
  • read and understand the Dutch language.

Exclusion criteria

  • previous lumbar spinal surgery
  • lumbar radicular syndrome
  • specific cause of low back pain
  • lumbar spinal stenosis
  • current malignancy
  • spondyloarthropathy
  • osteoporosis
  • spondylolisthesis
  • major trauma
  • infection
  • systemic disease.

Trial design

102 participants in 1 patient group

acute non-specific low back pain
Description:
patients with acute low back pain of (\< 6 weeks) were consecutively included with or without radiating pain, aged 18 to 60 years with a pain-free episode for at least 3 months before the onset of their current back pain. They were also required to be able to read and understand the Dutch language.
Treatment:
Other: In line with the Dutch guideline for non-specific low back pain, Standard usual care for non-specific low back pain was applied.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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