NCT07269925 Impact of Different Electrical Frequencies Used in Percutaneous Neuromodulation on Muscle Strength and Pressure Pain Thresholds
| NCT ID | NCT07269925 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Universidad Complutense de Madrid |
| Condition | Shoulder Pain |
| Study Type | INTERVENTIONAL |
| Enrollment | 30 participants |
| Start Date | 2026-02-15 |
| Primary Completion | 2026-06-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 30 participants in total. It began in 2026-02-15 with a primary completion date of 2026-06-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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
Inclusion Criteria: * 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. Exclusion Criteria: * 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. * Severe medical conditions (e.g., tumors, fractures, neurological or systemic diseases). * Clinically relevant asymmetries. * Generalized musculoskeletal conditions such as fibromyalgia.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07269925 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Shoulder Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07269925 currently recruiting?
Yes, NCT07269925 is actively recruiting participants. Contact the research team at juavaler@ucm.es for enrollment information.
Where is the NCT07269925 trial being conducted?
This trial is being conducted at Krakow, Poland, Nowy Targ, Poland.
Who is sponsoring the NCT07269925 clinical trial?
NCT07269925 is sponsored by Universidad Complutense de Madrid. The trial plans to enroll 30 participants.