Neurofeedback for Pain Sensitization in Knee Osteoarthritis

NCT ID
NCT07832682
Registry status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
Northeastern University
Conditions
Knee Osteoarthritis

Overview

ClinicalTrials.gov lists this study as Not yet recruiting.

Official title: Targeting Pain Sensitization in Knee Osteoarthritis by Conditioning the Endogenous Pain Control System Using Reflex Conditioning.

Enrollment: 50 participants (Estimated).

What is being studied

  • Other: FWR Down-Conditioning Neurofeedback
  • Other: Sham Feedback

Who may be eligible

Ages
45 Years to no maximum
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * Age 45 years or older * Symptomatic knee osteoarthritis meeting the clinical definition in the National Institute for Health and Care Excellence (NICE) guidelines: knee pain for more than 3 months and morning stiffness lasting less than 30 minutes * Able to speak and understand English * Able to attend all study visits at the study site in Boston, MA Exclusion Criteria: Stimulation safety * Pacemaker, implanted defibrillator, or other implanted electronic device * Metal implants in the head * Implants in the lower limb, including prior knee arthroplasty * History of seizures or epilepsy * Prior adverse reaction to transcranial magnetic stimulation * Frequent or severe headaches * Suspected or diagnosed cardiac disease * Pregnancy (self-reported) Neurological, psychiatric, and medical * Neurological disease, including multiple sclerosis * Currently active major depressive disorder, defined as a current clinical diagnosis of major depressive disorder or ongoing treatment for depression; a prior history that is neither active nor treated is not exclusionary * Insulin-dependent diabetes * Raynaud's phenomenon, cold urticaria, or other cold-induced reaction * Large ischaemic scars Pain and musculoskeletal * Lower extremity pain other than knee osteoarthritis Skin and sensation at stimulation sites * Altered skin sensation of the thigh * Swollen, infected, inflamed, or damaged skin of the thigh Substances * Use of medication known to alter pain perception or cortical excitability, including opioids, gabapentinoids, antidepressants (SSRIs, SNRIs, tricyclics), benzodiazepines, anti-seizure medications, muscle relaxants, prescription sleep medications, and cannabis or cannabinoids * Use of alcohol or recreational drugs within 12 hours before a study visit Radiographic confirmation is not required, consistent with current clinical recommendations for knee osteoarthritis diagnosis. Commonly used medications that do not alter pain perception or cortical excitability are permitted and recorded as covariates.

Study locations

No study locations are listed in the registry data.

Study details

Start date
October 1, 2026
Primary completion date
July 1, 2030
Completion date
July 1, 2031
First posted
September 22, 2026
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07832682
Registry last updated
September 22, 2026
QualifiedStudies registry data refreshed
October 5, 2026
QualifiedStudies record fetched
October 5, 2026

View NCT07832682 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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