Ireland
--:--IST
Recruiting Not applicable

The Effect of Early-Phase Graded Motor Imagery Following Massive Rotator Cuff Repair.

NCT07481864 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-03-15
Last updated
2026-07-15

Condition(s) studied

Shoulder Pain

Investigational drug(s) / intervention(s)

Graded Motor İmagery

Graded Motor İmagery: The graded motor imagery program will include laterality recognition training, motor imagery exercises, and mirror therapy tasks aimed at activating cortical motor networks without physical shoulder movement during the early postoperative phase.

Study summary

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. Graded motor imagery (GMI), a movement representation technique that includes laterality recognition, motor imagery, and mirror therapy, has been shown to modulate cortical processing and improve pain and motor function in various musculoskeletal and neurological conditions. However, its potential role in early postoperative shoulder rehabilitation has not been adequately investigated.

Eligibility

Sex
ALL
Min age
30 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Age between 30 and 65 years * Presence of an arthroscopically repaired anterior-superior rotator cuff tear, involving the supraspinatus and subscapularis tendons Exclusion Criteria: * 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

Primary outcome measure(s)

  • Pain Intensity (Numeric Rating Scale, NRS) — Baseline (postoperative day 0), 2 weeks, 4 weeks, 6 weeks, and 12 weeks after surgery.
    Pain intensity will be assessed using the Numeric Rating Scale (NRS), where participants rate their average shoulder pain over the past 24 hours on a scale from 0 (no pain) to 10 (worst imaginable pain). Pain will be evaluated at rest, during activity, and at night.
  • Subjective Shoulder Value (SSV) — Baseline (postoperative day 0), 2 weeks, 4 weeks, 6 weeks, and 12 weeks.
    Participants will rate the overall function of their shoulder on a 10-cm scale ranging from "as bad as it could be" to "as good as it could be."
  • Passive Shoulder Range of Motion — 4 weeks, 6 weeks, and 12 weeks after surgery.
    Passive shoulder range of motion will be measured using a goniometer.

Trial sites (1)

FacilityCityRegionStatus
Acibadem University Istanbul Turkey Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07481864 on ClinicalTrials.gov ↗ ← All trials in Turkey