Clinical Research Directory

Inclusion Criteria: 1. Adult subjects currently experiencing musculoskeletal pain with a Numeric Pain Rating Scale (NPRS) score of 4 or more at baseline. 2. Subjects are considered suitable to self-administer stimulation of motor nerves or stimulation of sensory nerves at home, based on the Investigator's judgement. 3. Subjects are suitable to receive treatment using the Compex SP8.0 device Pain management programs (pre-set parameters) for up to 4 weeks, based on the Investigator's judgement. 4. Subject, both male and female, ≥ 18 years of age at the time of consent 5. Subject has reviewed the IEC-approved consent form, has properly consented per the protocol and has documented their consent to participate in the study by signing the Ethics-approved consent form. 6. Subject does not meet any of the exclusion criteria Exclusion Criteria: 1. Pregnancy 2. Presence of Implanted electronic devices (e.g., pacemakers, defibrillators) 3. Skin conditions that contraindicate TENS use (e.g., rashes, wounds in electrode placement areas). 4. Known allergy to electrode materials. 5. Current participation in another clinical study that could interfere with this study's outcomes. 6. Subjects who are not able to read and understand the Instructions for Use, warnings, cautions and dangers 7. Subjects who are not able to read and understand indications and contraindications of the device 8. Subjects who are not able to sense auditory and visual signals 9. Subjects who are being treated with any other electrotherapy device for pain relief. 10. Subjects who are being treated with acupuncture 11. Participation in another clinical study within 30 days prior to screening