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Massage guns vs. manual therapy: which eases shoulder pain better?

NCT ID NCT07756203

Symptom relief Sponsor: Emre DANSUK Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 10, 2026 · Last updated Aug 26, 2026 · Updated 5 times

Summary

This trial compares two hands-on therapies—percussion massage with a handheld device and instrument-assisted soft tissue mobilization—when added to standard physiotherapy for people with shoulder impingement syndrome. About 48 adults aged 40–60 with confirmed impingement will be randomly assigned to one of three groups: physiotherapy alone, physiotherapy plus percussion massage, or physiotherapy plus instrument-assisted therapy. Over four weeks, researchers will measure changes in shoulder joint position sense, range of motion, pain, disability, and quality of life to see if the added therapies improve outcomes.

What this could mean

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

Active substance
Percussion massage therapy using a handheld Hypervolt device, and instrument-assisted soft tissue mobilization, each added to conventional physiotherapy
What this could lead to
If effective, these massage techniques could become standard add-ons to physiotherapy, helping people with shoulder impingement recover faster and with less pain.
What could go wrong
This is a small, early-stage trial, so results may not apply broadly. The therapies are unlikely to cause serious harm but may offer only modest benefits over standard care.

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 42 people

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

Started

Aug 2026

Expected to finish

Oct 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

40 to 60 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: * Men or women aged 40 to 60 years. * Diagnosis of subacromial impingement syndrome confirmed by clinical examination and -magnetic resonance imaging. * Positive Neer test. * Positive Hawkins-Kennedy test. * Positive painful arc test. * Shoulder symptoms persisting for at least one month. * Ability and willingness to participate in the assessment and intervention programme. * Provision of written informed consent. Exclusion Criteria: * Previous surgery involving the affected upper extremity. * Inflammatory joint disease. * Shoulder osteoarthritis. * Rheumatic disease. * Malignant or benign tumour affecting the shoulder region or upper extremity. * Open wound or active infection in the shoulder region. * Inability to tolerate vibration-based therapy. * Inability to comply with the study protocol or intervention programme.

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Conditions

The condition(s) this trial relates to.

shoulder impingement syndrome Shoulder Pain

As listed by the trial registrant

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

Impingement shoulder Impingement syndrome Shoulder 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

  • Istanbul Medipol University

    RECRUITING

    Istanbul, Beykoz, 34815, Turkey (Türkiye)

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