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EEG-based cortical oscillatory alterations in rotator cuff-related shoulder pain during rest and movement: a cross-sectional study

EEG-based cortical oscillatory alterations in rotator cuff-related shoulder pain during rest and movement: a cross-sectional study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128980
Enrollment
Unknown
Registered
2026-07-29
Start date
2026-09-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Rotator cuff-related shoulder pain

Interventions

rotator cuff-related shoulder pain, RCRSP group:None
Healthy group:None

Sponsors

Shanghai Seventh People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.RCRSP group: (1) Aged 35-75 years; (2) Shoulder pain persisting for at least 3 months; (3) Pain intensity rated =4/10 on the Numeric Pain Rating Scale(NPRS) in at least one of the following conditions: at rest, during activity, or night-time pain; (4) Right-handed; (5) Clinical presentation consistent with RCRSP, identified according to British Elbow and Shoulder Society (BESS) and a combination of physical examination findings; (6) Sign the informed consent form; 2.Healthy group: (1) Healthy controls will be age- and sex-matched to the RCRSP group; (2) Right-handed; (3) Sign the informed consent form; (4) Sign the informed consent form;

Exclusion criteria

Exclusion criteria: 1. Suspected acute or massive rotator cuff tears; 2. Presence of other primary shoulder disorders, such as primary adhesive capsulitis; 3. Cervical spine-related pain or neurological disease; 4. Previous history of shoulder surgery; 5. Received injection therapy within the past 1 month; 6. Major psychiatric disorder, clinically significant cognitive impairment; 7. Current use of centrally acting medications, or conditions contraindicating EEG recording; 8. History of malignancy or ongoing cancer treatment.

Design outcomes

Primary

MeasureTime frame
resting-state alpha-band mean power density within the predefined sensorimotor ROI;

Secondary

MeasureTime frame
Power Indicators of Other Frequency Bands in Resting State;Movement-evoked pain score;event-related desynchronization/synchronization (ERD/ERS);Resting-state functional connectivity indicators;Number of adverse events and severity grading;

Countries

China

Contacts

Public ContactLiming Jiang

Shanghai Seventh People's Hospital

qyjlm1487@163.com+86 176 2167 8676

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026