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20-Minute TENS zaps back pain and stiffness instantly?

NCT ID NCT07242235

Symptom relief Sponsor: Erzurum Technical University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether a single 20-minute session of TENS (a device that sends mild electrical pulses through the skin) can immediately reduce muscle stiffness and pain in people with long-lasting low back pain. About 24 adults aged 18–30 with non-specific low back pain will be randomly assigned to receive TENS or just rest. Researchers will measure changes in muscle stiffness and pain right after the session to see if TENS offers quick relief.

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

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

About 24 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Nov 2025

An estimate. Start dates often move.

Expected to finish

Dec 2025

An estimate. End dates often move.

Lead sponsor

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

18 to 30 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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: * Aged 18-30 years Non-specific low back pain persisting or recurring for ≥3 months Reported tenderness/stiffness on palpation of the lumbar erector spinae muscles Able to understand the study procedures and provide written informed consent Able to attend on the same day for TENS application and pre-/post-intervention measurements Exclusion Criteria: * Low back pain with a specific cause (e.g. lumbar disc herniation with radiculopathy, infection, tumor, fracture, severe deformity) Open wound, dermatitis, or any skin condition in the lumbar area that prevents electrode placement Presence of a cardiac pacemaker or other implanted electronic device Electrotherapy, injection, or manual therapy applied to the lumbar region within the previous 48 hours Pregnancy Severe neurological deficit or sensory loss Use of analgesics/NSAIDs at a level that may interfere with pain or stiffness assessment at the time of evaluation Any other condition deemed unsafe or inappropriate by the investigator

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Conditions

The condition(s) this trial relates to.

Low Back Pain

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Low back pain Lumbar muscle stiffness Non-specific low back pain

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Erzurum Technical University

    Erzurum, Turkey (Türkiye)

More trials for these conditions

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