Skip to content

A Neurofeedback Treatment for Chronic Musculoskeletal Pain

A Neurofeedback Treatment for Chronic Musculoskeletal Pain

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03863847
Enrollment
32
Registered
2019-03-05
Start date
2018-09-01
Completion date
2019-12-31
Last updated
2019-03-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Musculoskeletal Pain, Lateral Epicondylitis, Musculoskeletal Pain, Tennis Elbow

Keywords

Pain, Chronic Pain, Musculoskeletal Pain, Treatment, Neurofeedback, Brain Activity, Brain Oscillation, Brain Computer Interface

Brief summary

This study evaluates the effects of a novel neurofeedback treatment on pain specific brainwaves in adults. Chronic pain patients enrolled in this study will be randomized into a treatment group and a sham group.

Detailed description

Recent research has underlined that central nervous system structures play a key role in the development of pain with significant maladaptive plasticity occurring in several brain areas. Non-pharmacological treatments, such as neurofeedback, are designed to restore normal brain function alongside with relieving pain symptoms. With a neurofeedback approach, the patient is provided with a feedback on specific brain waves recorded using non-invasive recording techniques (electroencephalography - EEG) and visualized on a screen.

Interventions

PROCEDURENeurofeedback

The patients will receive neurofeedback on pain related brain-activity, and through training, learn to control said brain-activity.

PROCEDURESham

The patients will receive sham neurofeedback on non-pain related brain-activity, and through training, learn to control said brain-activity.

Sponsors

Aalborg University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Patients suffering from chronic pain due to tennis elbow for at least 3 months * A clinical diagnosis of chronic lateral epicondylalgia, * Pain associated with functional activities such as gripping and pain with resisted contraction of the wrist extensors or extensor carpi radialis brevis, or with passive stretching of the wrist extensors.

Exclusion criteria

* Clinical diagnosis of chronic lateral epicondylalgia on both sides, cervicothoracic spinal pathology, other upper limb musculoskeletal disorders or neurological disorders * Pregnancy * Drug addiction defined as the use of cannabis, opioids or other drugs * Previous or current neurologic, musculoskeletal or mental illnesses defined as an on-going systemic condition * Lack of ability to cooperate * Current use of medications that may affect the trial e.g. analgesics, anti- inflammatory drugs * Consumption of alcohol, caffeine, nicotine or painkillers throughout the study period * Past history of chronic pain, neurological or psychiatric conditions * Participation in other pain trials throughout the study period and one month prior to participation * Participation in more than two sessions of muscle training exercises per week involving the upper limb and/or lower back * Evidence of other sources of elbow pain such as exacerbation of pain with neck movement or manual examination * Sensory disturbances * History of fractures * Elbow surgery * Contraindications to the use of TMS

Design outcomes

Primary

MeasureTime frameDescription
Visual Analogue Scale (VAS)Up to three monthsNumerical pain scale ranging from 0 being no pain to 10 being worst imaginable pain (significant change in VAS score will be set to 1 at P = 0.05)

Secondary

MeasureTime frameDescription
Electromyographic (EMG) measurement.Up to three monthsEMG electrodes will be applied to the Extensor Carpi Radials Brevis (ECRB) muscle, to provide movement temporal features for EEG extraction.
Electroencephalographic (EEG) measurement. International 10-20 electrode placement with 10 channels placed on the contralateral hemisphere to the dominant limb being tested.Up to three monthsQuantitative brain activity analysis to provide the subject with real-time feedback of their brain activity. The neurofeedback group will receive feedback on alpha brainwave power and learn to control this, while the sham group will receive feedback on non-pain related brain activity.

Countries

Denmark

Contacts

Primary ContactNatalie Mrachacz Kersting, Dr
nm@hst.aau.dk+4599407571
Backup ContactMorten Kirkegaard, BsC
mkirk14@student.aau.dk+4620468932

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026