Could a tiny needle zap away shoulder pain? new trial tests best frequency
NCT ID NCT07269925
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compares two electrical frequencies (high vs. low) used in percutaneous electrical nerve stimulation (PENS) for shoulder pain. Thirty adults with a trigger point in the infraspinatus muscle will receive a single session, and researchers will measure changes in muscle strength and pain sensitivity. The goal is to find the optimal dosage for this technique, which is still being explored for chronic pain.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Percutaneous electrical nerve stimulation (PENS) at high or low frequency
- What this could lead to
- If successful, this could help identify the best electrical frequency for easing shoulder pain and improving muscle strength using a needle-based stimulation technique.
- What could go wrong
- This is a small, early-phase study with only 30 participants and no control group, so results may not apply broadly. The technique is still experimental and its benefits over standard treatments are not proven.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- Expected to finish
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Jul 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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ATMIS
NOT_YET_RECRUITINGKrakow, Poland, Poland
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ATMIS
RECRUITINGNowy Targ, 34-400, Poland
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