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New treatment option for Shoulder Pain
Official title The Effect of Early-Phase Graded Motor Imagery Following Massive Rotator Cuff Repair.
ClinicalTrials.gov ID: NCT07481864
What this study is testing
- What it's testing
- Massive rotator cuff tears are associated with significant pain, functional limitations, and prolonged rehabilitation following surgical repair. In the early postoperative phase, rehabilitation protocols are often limited due to surgical protection requirements, which may delay the restoration of motor control and shoulder function.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 30 to 65
You may be able to join if
- Age between 30 and 65 years
- Presence of an arthroscopically repaired anterior-superior rotator cuff tear, involving the supraspinatus and subscapularis tendons
You likely can't join if
- Age younger than 30 years or older than 65 years
- Presence of severe malignant, hematological, endocrine, metabolic, rheumatologic, or gastrointestinal diseases
- Diagnosis of glenohumeral osteoarthritis (Kellgren-Lawrence grade III or higher, with radiographic evidence of osteophytes)
- Current treatment with cytotoxic agents or systemic corticosteroids
- Alcohol dependence, history of substance abuse, or psychological/emotional disorders that may compromise the validity of informed consent
- Previous surgery on the ipsilateral shoulder
See the full eligibility criteria
- Age between 30 and 65 years
- Presence of an arthroscopically repaired anterior-superior rotator cuff tear, involving the supraspinatus and subscapularis tendons
- Age younger than 30 years or older than 65 years
- Presence of severe malignant, hematological, endocrine, metabolic, rheumatologic, or gastrointestinal diseases
- Diagnosis of glenohumeral osteoarthritis (Kellgren-Lawrence grade III or higher, with radiographic evidence of osteophytes)
- Current treatment with cytotoxic agents or systemic corticosteroids
- Alcohol dependence, history of substance abuse, or psychological/emotional disorders that may compromise the validity of informed consent
- Previous surgery on the ipsilateral shoulder
- Multiple tendon tears, such as combined tears involving the supraspinatus together with the infraspinatus or subscapularis tendons
The study team makes the final eligibility decision.
Where it's taking place
- Istanbul, Turkey, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 30 years to 65 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Istanbul, Turkey, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.