Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Brooke Army Medical Center
Age
18–62
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
active duty Service Members (SMs) between the ages of 18 and 62, inclusive
history of chronic LBP (i.e. intermittent or continuous LBP symptoms present for 3 months or greater prior to entry into the study
participants must be using narcotic and/or non-narcotic oral analgesic medications to treat their chronic LBP symptoms on a weekly basis
must be able to speak and read English and understand the study procedures
You may not be if
pacemaker or implanted electronic device
history of stroke, blood clots, or cardiac arrhythmias
pregnancy
no self-reported history of prescription medication abuse or sole-provider contract for prescribed narcotic medications
open wound over site of chronic pain;
history of spinal surgery
participation in a clinical trial for an investigational drug/ treatment within last 30 days
undergone treatment with TENS, biofeedback, or acupuncture within last 30 days
prior treatment with the Biomodulator
LBP "red flags": fever, trauma, progressive motor or sensory deficit, saddle anesthesia
participation in the study would delay the medical board (MEB) processing of the service member off of active duty status or would delay a return to duty status to their home unit
