About this trial
Percutaneous electrical nerve stimulation (PENS) involves delivering electrical currents through fine filiform needles inserted near tissues such as muscles, ligaments, or nerves. It has been explored for various chronic pain conditions affecting the cervical and lumbar spine, as well as the upper and lower limbs. Despite its growing clinical use, the overall quality of evidence supporting PENS for chronic musculoskeletal pain remains limited. Most studies have applied the technique directly over nerve structures, and while some reviews have shown greater pain reduction compared to transcutaneous electrical nerve stimulation (TENS), the superiority of PENS has not been conclusively demonstrated. Research specifically examining its application on nerve tissues, particularly in the upper limbs, remains scarce. Some preliminary and single-case studies have reported improvements in pain and disability following PENS directed at the radial nerve, but these findings are limited by small sample sizes and the absence of control groups. The physiological mechanisms underlying PENS are still not fully understood, though both peripheral and central processes are believed to be involved. Evidence suggests that PENS can reduce local sensitivity to pressure pain through peripheral mechanisms and may also enhance descending inhibitory control by activating conditioned pain modulation at the central level. However, further studies are necessary to clarify these effects.
Since to date, limited research has specifically examined the optimal PENS dosage, the present study aimed to compare two PENS dosage for improving muscle strength and pain pressure thresholds.
Eligibility criteria
Qualifiers
Presence of at least one latent myofascial trigger point (MTrP) in the infraspinatus muscle, identified according to the most recent Delphi consensus criteria.
Ability to read, understand, and sign the written informed consent form.
Disqualifiers
Current pharmacological treatment that may affect muscle tone.
History of shoulder or spinal surgery.
Traumatic disorders such as whiplash-associated injuries, dislocations, or fractures.
Neuropathies, including radiculopathies or myelopathies.
Trial design
Treatments tested in this trial
- Percutaneous electrical nerve stimulation: High frequency
- Percutaneous electrical nerve stimulation: Low frequency
Treatment groups
Sponsors and collaborators
Universidad Complutense de Madrid
Lead sponsor
Universidad Rey Juan Carlos
Collaborator