Massage gun vs. hands: which eases 'Text Neck' pain best?

NCT ID NCT07705711

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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
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Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
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The trial has finished. Results may not be published yet.
Stopped early
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Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

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Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
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When the status isn't known

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First seen Jul 15, 2026 · Last updated Jul 16, 2026 · Updated 1 time

Summary

This study compares the immediate effects of traditional hands-on massage and percussive massage (using a TheraGun device) on neck pain, flexibility, and satisfaction in young adults with text neck syndrome. Participants are university students aged 18–30 who use mobile devices heavily and report symptoms like neck pain, headaches, or shoulder pain. The goal is to see which approach provides faster relief and better mobility.

What this could mean

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

Active substance
classical massage and percussive massage (TheraGun)
What this could lead to
If one method proves more effective, it could offer a simple, at-home option for managing text neck pain without medication.
What could go wrong
This is a small, short-term study with only 34 participants, so results may not apply broadly. The effects measured are immediate, not long-term.

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 34 people

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

Expected to start

Aug 2026

An estimate. Start dates often move.

Expected to finish

Nov 2026

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

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * University students aged between 18 and 30 years. * Willing to participate in the study and provide informed consent. * Have been using a mobile device for at least 1 year. * Have no communication impairments. * Use a mobile device for at least 3 hours per day. * Report at least three of the six core symptoms of Mobile Neck Syndrome (MNS): neck pain, upper back pain, shoulder pain, headache, insomnia, and tingling or numbness in the hands. * Have a Neck Disability Index (NDI) score of 10 or higher. Exclusion Criteria: * History of generalized joint disorders affecting the head, neck, or shoulder region. * History of radiotherapy involving the head, neck, or shoulder region. * History of surgery involving the head or neck region. * Diagnosis of cervical disc herniation, cervical radiculopathy, or cervical myelopathy. * History of inflammatory, neuromuscular, or congenital disorders affecting the head or neck region. * Presence of a metal implant in the treatment area. * Current use of analgesics, muscle relaxants, anticoagulants, or other medications that may influence the study outcomes. * History of systemic disease. * Receipt of any treatment targeting the cervical region within the previous 3 months. * Pregnancy.

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Conditions

The condition(s) this trial relates to.

Neck Pain Pain

As listed by the trial registrant

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

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