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Tape or needle? study seeks best fix for shoulder pain

NCT ID NCT07190768

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 26, 2026

Summary

This study compares two common therapies—kinesio taping and dry needling—for treating subacromial pain syndrome, a frequent cause of shoulder pain. Researchers will enroll 100 adults aged 18-65 with shoulder pain lasting over 6 weeks. The goal is to see which approach, or a combination, reduces pain and improves shoulder function best.

What this could mean

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

Active substance
kinesio taping and dry needling
What this could lead to
If successful, this could show which therapy—taping, needling, or both—works best for easing shoulder pain and improving movement.
What could go wrong
This is a small, early-stage trial with only 100 participants, so results may not apply to everyone. Pain relief may vary, and some people might not respond to either treatment.

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 100 people

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

Expected to start

Oct 2025

An estimate. Start dates often move.

Expected to finish

Oct 2026

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 65 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: Age 18-65 years Pain in the upper, outer arm, especially during shoulder elevation Shoulder pain lasting more than 6 weeks with or without partial rotator cuff tear At least three of the following findings: Painful arc during flexion or abduction Positive Neer test Positive Hawkins-Kennedy test Painful resisted external rotation Positive Jobe's test Diagnosis confirmed by MRI evaluation when indicated Exclusion Criteria: Participation in a physical therapy program or receipt of injection therapy within the past 3 months Previous shoulder surgery Presence of joint contracture Complete tendon rupture Cervical radiculopathy Systemic inflammatory disease (e.g., rheumatoid arthritis, ankylosing spondylitis) Known allergy to tape or materials used in interventions Bleeding disorders Local infection or open wound in the treatment area Cognitive dysfunction that prevents cooperation History of malignancy

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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

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  1. 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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  2. A doctor treating you

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