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Longitudinal Change in Depression Severity and Clinical Outcomes After Arthroscopic Rotator Cuff Repair

Longitudinal Change in Depression Severity and Its Association With Clinical Outcomes After Arthroscopic Rotator Cuff Repair: A Prospective Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07769554
Enrollment
84
Registered
2026-08-18
Start date
2013-02-01
Completion date
2017-01-31
Last updated
2026-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depressive Symptoms, Rotator Cuff Tears

Keywords

rotator cuff repair, arthroscopy, depression, Hamilton Depression Rating Scale

Brief summary

This prospective cohort study evaluated how depressive symptom severity changes during the first 2 years after arthroscopic rotator cuff repair, and whether changes in depressive symptoms are associated with improvements in shoulder pain and function. Adults who underwent arthroscopic suture-bridge repair for a symptomatic full-thickness rotator cuff tear were classified by preoperative Hamilton Depression Rating Scale (HDRS) score as having depressive symptoms (HDRS ≥8) or not (HDRS ≤7). Depressive symptom severity (HDRS), shoulder pain (visual analog scale), and shoulder function (American Shoulder and Elbow Surgeons score and Constant score) were assessed before surgery and at 3, 6, 12, and 24 months after surgery. Integrity of the repaired tendon was evaluated with ultrasonography at 24 months.

Interventions

Arthroscopic repair of a full-thickness rotator cuff tear using a suture-bridge technique with medial-row suture anchors and lateral-row knotless anchors, performed as standard care in all participants

Sponsors

Chuncheon Sacred Heart Hospital
Lead SponsorOTHER
Hallym University Medical Center
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change in Hamilton Depression Rating Scale (HDRS) ScorePreoperatively (within 2 weeks before surgery) and at 3, 6, 12, and 24 months after surgeryClinician-administered rating scale of depressive symptom severity; higher scores indicate more severe depressive symptoms. A score of 8 or higher was defined as the presence of depressive symptoms.

Secondary

MeasureTime frameDescription
Visual Analog Scale (VAS) Score for PainPreoperatively (within 2 weeks before surgery) and at 3, 6, 12, and 24 months after surgeryScore range 0-10; higher scores indicate more severe pain.
American Shoulder and Elbow Surgeons (ASES) ScorePreoperatively (within 2 weeks before surgery) and at 3, 6, 12, and 24 months after surgeryScore range 0-100; higher scores indicate better shoulder function.
Constant ScorePreoperatively (within 2 weeks before surgery) and at 3, 6, 12, and 24 months after surgeryScore range 0-100; higher scores indicate better shoulder function.
Retear of the Repaired Rotator Cuff on Ultrasonography24 months after surgeryRetear was defined as complete discontinuity of the repaired rotator cuff tendon on ultrasonography.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 19, 2026