Can treating the mind heal the shoulder? a surgery study investigates
NCT ID NCT07769554
First seen Aug 18, 2026 · Last updated Aug 19, 2026 · Updated 1 time
Summary
This study follows adults having arthroscopic rotator cuff repair to see how their depression symptoms change over two years and whether those changes relate to shoulder pain and function. Participants are grouped by pre-surgery depression scores, then tracked at regular intervals. The goal is to understand if mental health influences physical recovery after this common surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Arthroscopic suture-bridge rotator cuff repair (a surgical procedure to fix a torn shoulder tendon)
- What this could lead to
- If mood changes track with shoulder recovery, it could point to mental health support as part of post-surgery care to improve outcomes.
- What could go wrong
- This is an observational study, so it can't prove cause and effect. Results may not apply to all patients, and depression measures can vary.
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.
- Participants
-
84 people
The number who actually took part.
- Started
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Feb 2013
- Finished
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Jan 2017
- Lead sponsor
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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.
Who is studied
Adults who underwent primary arthroscopic suture-bridge repair for a symptomatic full-thickness rotator cuff tear at a single tertiary referral hospital in the Republic of Korea between February 2013 and January 2015.
- Ages
-
Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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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: * Primary arthroscopic suture-bridge repair for a symptomatic full-thickness rotator cuff tear identified on preoperative MRI * Assessment of depressive symptom severity with the Hamilton Depression Rating Scale within 2 weeks before surgery * Willingness to complete scheduled follow-up assessments, including HDRS and clinical scores at 3, 6, 12, and 24 months and shoulder ultrasonography at 24 months after surgery Exclusion Criteria: * Partial-thickness rotator cuff tear or isolated subscapularis tear * Revision rotator cuff surgery * Shoulder instability * Glenohumeral osteoarthritis * Neurologic or systemic disease affecting the shoulder joint * History of acute trauma or infection * Incomplete medical records
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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.
Contacts and locations
Locations
-
Hallym University Chuncheon Sacred Heart Hospital
Chuncheon, Gangwon-do, 24258, South Korea
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can brain activity reveal why some people with depression lose motivation and pleasure?
- Does a camera lens offer a path to calmer minds?
- AI chatbot in schools may break down teen depression stigma
- MRI and biomarkers may predict rotator cuff repair success
- Can mindfulness tame diabetes distress and blood sugar?
- Can targeted nerve blocks ease shoulder surgery pain?