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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