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Completed

NCT Number: NCT01540617

The Neural Basis of Lumbosacral Proprioceptive Impairment in Recurrent Low Back Pain

Low back pain (LBP) is a well known health problem in Western society that is significantly responsible for socio-economic problems like absenteeism and disability. The lifetime prevalence of LBP is 60-80% and approximately 85% of this LBP has a "non-specific" character whereby the underlying causes and risk factors cannot be demonstrated. While many people recover within a month, most individuals will have recurrence within a year with more severe symptoms. This might be due to insufficient knowledge of the underlying mechanisms. Impaired proprioception, the ability to discern body/limb positions and movements, may cause and maintain LBP shown by an altered postural control strategy. Specifically, patients with LBP rely more on proprioceptive signals from the ankles due to less reliable proprioceptive input of proximal segments. Moreover, they show a decreased variability in postural control and less postural robustness, while variability is a prerequisite for optimal functioning of biological systems. However, further clarification of the neural correlates is necessary. Deficits in proprioception, as found in a subgroup of patient with LBP, are associated with a decreased ability of the brain to process proprioceptive inputs.

The aim of this project is to clarify the central changes in individuals with recurrent non-specific low back pain and healthy controls. To evaluate these central changes MRI techniques (3DTFE, DTI and RS-fMRI) will be used. In addition, the association between central changes and postural control tasks will be evaluated.

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Key information

Age range

20 year–50 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Katholieke Universiteit Leuven

Leuven, 3000, Belgium

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

persons with low back pain:

  • Age: 20-50 year
  • At least 6 months of low back pain with/without referred pain in buttock/thigh
  • At least 3 episodes of disabling low back pain
  • At least a score of 14% on the Oswestry Disability Index
  • Willingness to sign the informed consent
  • Met the MRI related requirements

Inclusion criteria

healthy persons:

  • Age: 20-50 year
  • No history of low back pain
  • A score of 0% on the Oswestry Disability Index
  • Willingness to sign the informed consent
  • Met the MRI related requirements

Exclusion criteria

  • History of major trauma and/or major orthopedic surgery of the spine, the pelvis or the lower quadrant
  • One of the following conditions: Parkinson, MS, Stroke with sequels....
  • Radicular symptoms
  • Not Dutch-speaking
  • Strong opioids
  • Neck pain
  • Ankle problems
  • Smoking

Treatment and study plan

Primary outcomes

  1. Structural changes in white matter pathways (3DTFE and DTI) (in individuals with recurrent non-specific low back pain compared to healthy controls)

    Time frame: One time point

  2. Changes in resting state activity between individuals with recurrent non-specific low back pain and healthy controls)

    Time frame: One time point

  3. Proprioceptive postural control (center of pressure displacement in response to muscle vibration)

    Time frame: One time point

Sponsors and collaborators

Lead sponsor

KU Leuven

Other

Collaborators

  • Agentschap voor Innovatie door Wetenschap en Technologie

Registry information

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
Feb 29, 2012
Registry last updated
Apr 14, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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