Could a simple back move ease shoulder pain? new trial tests the idea
NCT ID NCT07525297
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether adding a gentle back-mobilization technique to standard shoulder therapy can improve pain, movement, and function in people with rotator cuff injuries. Forty adults with chronic shoulder pain will receive either shoulder mobilization alone or combined with thoracic spine mobilization over three weeks. The goal is to see if treating the whole shoulder-upper back chain works better than focusing only on the shoulder.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Manual therapy techniques (Mulligan mobilization with movement and thoracic spine mobilization)
- What this could lead to
- If this works, it could show that adding a simple back-mobilization technique to standard shoulder therapy provides better pain relief and movement for people with rotator cuff problems.
- What could go wrong
- This is a very small, early-stage trial with only 40 participants and a short 3-week follow-up. Results may not apply to everyone, and the benefit over standard care alone may be small or nonexistent.
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 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Apr 2026
An estimate. Start dates often move.
- 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
-
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 Hide 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: * Having been diagnosed with unilateral rotator cuff pathology (impingement syndrome, tendinopathy, or partial tear) by a specialist physician through clinical examination and/or radiological imaging (USG/MR); * Being between 18 and 65 years of age; * Having shoulder pain that has persisted for at least 3 months; * Having a positive result on at least two of the Neer, Hawkins-Kennedy, and Empty Can tests; * Having a pain intensity of at least 3/10 on the Pain Numerical Rating Scale (NPRS) during rest or activity; * Having sufficient cognitive ability to follow simple instructions and administer the tests; * Having a Mini Mental State Test score ≥24; * Having the ability to provide signed informed consent and agreeing to participate in the study voluntarily. Exclusion Criteria: * Having undergone previous surgery on the shoulder or thoracic region; * Having full-thickness rotator cuff tears requiring surgical indication; * Having adhesive capsulitis, shoulder instability, labrum tears, or calcific tendinitis; * Having cervical radiculopathy or neurological diseases affecting the upper extremity; * Having uncontrolled diabetes, inflammatory rheumatic diseases (rheumatoid arthritis, etc.), or malignancy; * Having severe osteoporosis, unstable vertebral fractures, or active infection in the thoracic region; having received steroid (cortisone) or PRP injections to the shoulder region within the last 3 months.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Rotator cuff injuries are added.
Genom att skicka in godkänner du våra Användarvillkor
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
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
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
-
Van Yüzüncü Yıl University
Van, Tuşba, 65080, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can your beliefs about pain shape your shoulder disability?
- Could core strength hold the key to shoulder recovery?
- Could a simple steroid injection replace a catheter for shoulder surgery pain?
- Patch aims to cut rotator cuff Re-Tear rate after surgery
- Shoulder surgery debate: to repair or not to repair the rotator cuff?
- Which Non-Surgical treatment eases shoulder calcium pain best?