Hands-On or electrotherapy? trial tests two approaches for stubborn neck pain

NCT ID NCT07695402

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 10, 2026 · Last updated Jul 15, 2026 · Updated 2 times

Summary

This trial investigates whether a manual therapy called the Jones Technique, a combination of ultrasound and TENS, or both together can reduce neck pain caused by muscle knots in the upper back. The study includes women aged 18 to 40 with active trigger points and neck pain lasting less than three months. Researchers measure pain, arm function, sleep quality, and quality of life to see which approach works best.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Jones Technique (manual therapy) and Combined Therapy (therapeutic ultrasound plus TENS)
What this could lead to
If effective, these therapies could offer drug-free options for easing neck pain and improving sleep and daily function in women with myofascial trigger points.
What could go wrong
This is a small, early-stage trial with only 40 participants, so results may not apply broadly. The treatments may provide only temporary relief or no benefit over sham.

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

40 people

The number who actually took part.

Started

Oct 2024

Finished

Dec 2024

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 40 years

Sex

Female participants only

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: * Female participants aged 18 to 40 years. * Presence of active myofascial trigger points in the upper trapezius muscle for no longer than 12 weeks. * Neck pain lasting less than 3 months. * Pain intensity of at least 3 cm on the 10-cm Visual Analog Scale (VAS). * Ability to understand the study procedures and provide written informed consent. Exclusion Criteria: * Presence of a cardiac pacemaker or other contraindications to electrotherapy. * Pregnancy. * Uncontrolled cardiovascular disease. * Psychiatric disorders that could interfere with study participation. * Thrombosis or coagulation disorders. * History of tumors or neoplasms. * Physical therapy or myofascial treatment within the previous 3 weeks. * Treatment for myofascial trigger points within the previous 3 months. * Current use of analgesic medications. * Cervical musculoskeletal disorders (e.g., cervical osteoarthritis or other cervical lesions). * History of cervical trauma or surgery. * Cervical spondylosis or spondylolisthesis with radiculopathy. * Fibromyalgia or other systemic rheumatic diseases. * Other musculoskeletal disorders that could interfere with the study outcomes.

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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.

Contacts and locations

Locations

  • Physical Therapy Teaching Clinic, Universidade do Vale do Rio dos Sinos (UNISINOS)

    São Leopoldo, Rio Grande do Sul, Brazil

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