Clinical Research Directory

Inclusion Criteria: * Diagnosed with LBP with an average pain score of 4 or higher on DVPRS for \> 3 months * Ability to sit or lay down for 30 minutes during treatments * Demonstrated ability to correctly use the device and maintain adequate sensor contact throughout (assisted or unassisted) * Female participants who could possibly become pregnant must agree to use a highly effective contraceptive method from the screening period through the 4 weeks of study intervention and any use during the wait-list control period. These methods include a physical barrier method (e.g., condom) plus an additional hormonal, IUD, tubal ligation, or second type of barrier (e.g., diaphragm). In addition, they must abstain from egg collection or donation during the same period. Exclusion Criteria: * Individuals \< 18 or \>70 years of age at enrollment * Persons with Pacemakers, or interstitial pumps, or spinal cord stimulator in ON mode. * Persons who have received back surgery (open) within the last 3 months * Pregnant or sexually active female subjects who could possibly become pregnant and who are not willing to use an acceptable form of contraception (barrier method plus one of the following: second barrier, hormonal, IUD, or tubal ligation).