Actively Recruiting
Impact of Different Electrical Frequencies Used in Percutaneous Neuromodulation on Muscle Strength and Pressure Pain Thresholds
Led by Universidad Complutense de Madrid · Updated on 2026-05-08
30
Participants Needed
2
Research Sites
23 weeks
Total Duration
On this page
Sponsors
U
Universidad Complutense de Madrid
Lead Sponsor
U
Universidad Rey Juan Carlos
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Impact of Different Electrical Frequencies Used in Percutaneous Neuromodulation on Muscle Strength and Pressure Pain Thresholds
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Presence of at least one latent myofascial trigger point in the infraspinatus muscle as identified by Delphi consensus criteria
- Ability to read, understand, and sign the written informed consent form
You will not qualify if you...
- Current use of medications that may affect muscle tone
- History of shoulder or spinal surgery
- Traumatic injuries such as whiplash, dislocations, or fractures
- Presence of neuropathies including radiculopathies or myelopathies
- Severe medical conditions such as tumors, fractures, neurological or systemic diseases
- Clinically relevant asymmetries
- Generalized musculoskeletal conditions like fibromyalgia
AI-Screening
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Trial Site Locations
Total: 2 locations
1
ATMIS
Krakow, Poland, Poland
Not Yet Recruiting
2
ATMIS
Nowy Targ, Poland, 34-400
Actively Recruiting
Research Team
J
Juan Antonio Valera-Calero, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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