Pain, Acute, Pain, Chronic, Pain, Experimental
Conditions
Keywords
Transcranial Magnetic Stimulation, Focused Ultrasound, Noninvasive Neuromodulation
Brief summary
Non-invasive brain stimulation techniques, transcranial magnetic stimulation (TMS) and transcranial focused ultrasound (FUS), is be applied to healthy human subjects, acute pain patients, and chronic pain patients to investigate their uses for pain relief.
Detailed description
The research team will be using non-invasive brain stimulation techniques, transcranial magnetic stimulation (TMS) and transcranial focused ultrasound (FUS) to investigate their uses for pain relief in humans: healthy human subjects, acute pain patients, and chronic pain patients. Magnetic Resonance Imaging (MRI) and electroencephalogram (EEG) recordings will be collected to achieve the following objectives: Objective 1 aims to determine the effects of noninvasive brain stimulation on the pain-related brain activities during pain processing. We hypothesize that noninvasive brain stimulation approaches will increase or decrease cortical activity upon processing painful input. Objective 2 aims to determine the effects of noninvasive brain stimulation on pain intensity and/or pain-related behavioral assessments. We hypothesize that noninvasive brain stimulation will influence pain-intensity and/or pain-related behavioral assessments. Objective 3 aims to investigate the correlation between brain activity and pain relief after noninvasive brain stimulation. We hypothesize that noninvasive brain stimulation will suppress cortical activity in pain-related brain areas, reduce pain intensity, and/or improve pain-related behavioral assessments.
Interventions
Non-invasive brain stimulation technique
OTHERTranscranial Magnetic Stimulation
Non-invasive brain stimulation technique
Sponsors
University of Virginia
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)
Intervention model description
Within subjects design of real and control stimulation, pain measures and behavioral assessments may be compared between healthy subjects and pain groups.
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes
Inclusion criteria
* Healthy adults between 18 and 80 years of age. * Chronic and Acute pain patients: must have an MRI (for ultrasound targeting)
Exclusion criteria
* Direct report to the study team member * History of brain surgery * History of seizure * Pregnant * Have alcohol consumption exceeding 50 drinks/month * Have history of opioid abuse (all subjects), or any recent opioid use (healthy controls) * Have implant like pacemaker and aneurysm clip * Current of psychiatric disease such as anxiety or depression, which is not optimally treated * Current infection * Current wound on the skin of upper and lower extremities * Chronic pain patients: current chronic pain is not optimal controlled by pain medications (i.e. Pain VAS \>5)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Numeric Pain Rating Scale | immediately after brain stimulation (same day, approximately 5-10 minutes after baseline) as compared to baseline | Participants will rate their pain (experimental, acute, chronic) on a 1-10 scale |
Countries
United States
Outcome results
None listed