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Completed

NCT Number: NCT02678494

Brain-Train Home Based Pain Treatment

A study examining the effectiveness of neurofeedback therapy for the treatment of Central Neuropathic Pain (CNP), in patients with a Spinal Cord Injury, using a small user-friendly device which can be operated by patients at home.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Queen Elizabeth National Spinal Injuries Unit

Glasgow, United Kingdom

About this study

Spinal Cord Injury (SCI) affects a person's ability to move and feel sensation from the body. SCI is also an indirect cause of a persistent pain, called Central Neuropathic Pain (CNP). This pain typically develops several months after the injury.

In 30% to 40% of SCI patients, severe CNP affects their everyday living including sleep and mood. Medical treatment of CNP is moderately effective and costly, both to the patient and to the health care system.

In a previous study, some characteristic 'signatures' of brain waves that are related to CNP were defined. Based on this, a novel treatment for CNP based on neurofeedback was developed and clinically tested on five SCI patients. Electroencephalograph (EEG) was used to record patients' brain waves and shown to patients on a computer screen in a simple graphical form (e.g. bars). Patients were trained to change their brain activity at will and, as a consequence, their pain was reduced. Costly laboratory devices were used and once the study was over, an adequate alternative could not be offered to patients.

In this study, a cheap, portable, wireless and user friendly, Conformité Européenne (CE) marked EEG device will be used to train 10 patients to self-administer the therapy in the comfort of their homes. Participants will be given initial training to use the equipment then will be asked to use the system at home for 3 months - initially, 3-5 times a week then, if/when pain subsides, at least once a week or as required.

The primary purpose of the study is to determine whether a portable system for neuromodulation is a useful tool for administering therapy for pain (intensity of pain will be measured by the visual numerical scale (VNS)).

The secondary purpose of the study is a quantitative analysis of changes in the brain activity due to therapy, as measured by EEG; patients' perspective of the home based neuro-therapy (assessed by questionnaires and one-to-one, semi-structured interviews).

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • normal or corrected to normal vision
  • no history of brain disease or injury
  • incomplete/complete injury at level C5 to T12
  • central neuropathic pain (below the level of injury)
  • intensity of pain 4 or above (VNS)
  • stable medication regime (expected not to change during the period of the study), responding to some extent to CNP medication treatment
  • patient or caregiver minimum computer literacy (owning a computer, laptop, tablet, ipad etc)

Exclusion criteria

  • chronic or acute muscular or visceral pain larger than 4 VNS
  • epilepsy
  • diagnosed mental health problems
  • active intervention of pain team (changing existing treatments)

Treatment and study plan

Neurofeedback training

Other

Primary outcomes

  1. Pain intensity

    Time frame: Baseline and 3 months

    Change in intensity of pain as measured by the Visual Numerical Scale

Secondary outcomes

  1. Brain activity

    Time frame: Baseline and 3 months

    Change in brain activity as measured by EEG

  2. Patients' perspective of home-based neuro-therapy training

    Time frame: 3 months

    Qualitative assessment of patient's perspective of treatment as assessed by questionnaire and one-to-one semi-structured interview

Sponsors and collaborators

Lead sponsor

NHS Greater Glasgow and Clyde

Other

Registry information

Official study title

Home Based Brain-Train Treatment of Central Neuropathic Pain Following Spinal Cord Injury

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Feb 9, 2016
Registry last updated
Sep 4, 2018

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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