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Exercise Rehabilitation Intervention for Rotator Cuff Injuries

Exercise Rehabilitation Intervention for Rotator Cuff Injuries

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120039
Enrollment
Unknown
Registered
2026-03-09
Start date
2025-03-10
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Rotator cuff injury

Interventions

Control Group:TBHM (including soft tissue release, trigger point therapy, rocking, pulling, flexion and rotation manipulation, shoulder adjustment, and finishing techniques) combined with conventional
Trial Group:TBHM combined with scapular muscle correction training (including scapular positioning isometric contraction training, bilateral scapular muscle co-contraction isotonic training, downward

Sponsors

Hefei Normal University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 36 Years

Inclusion criteria

Inclusion criteria: 1. Athletes engaged in sports-related activities with training duration exceeding 6 months; 2. Patients aged 16–30 years, with symptom duration of 12–24 weeks; 3. Patients diagnosed with grade I or II rotator cuff injuries confirmed by shoulder MRI or ultrasound; 4. Patients with rotator cuff injury accompanied by scapular dyskinesis (Kibler types I, II, or III); 5. No surgery or other interventions potentially affecting study outcomes received within 1 month prior to or during the intervention period; 6. Patients provided informed consent and signed the consent form for participation in this study.

Exclusion criteria

Exclusion criteria: 1. Patients with shoulder skin diseases or severe skin damage/ulceration; 2. Patients with a history of shoulder fracture or surgery; 3. Patients with severe cardiovascular/cerebrovascular diseases, cardiopulmonary dysfunction, tumors, or bone metastasis; 4. Patients with differential diagnoses such as cervical spondylosis or frozen shoulder; 5. Patients with complete or substantial rotator cuff tears identified on imaging studies; 6. Patients who withdraw from the study mid-course or fail to comply with required assessments and rehabilitation protocols.

Design outcomes

Primary

MeasureTime frame
Constant-Murley score,CMS;Shoulder blade motion parameters;Isokinetic muscle strength testing;

Secondary

MeasureTime frame
Visual analogue score,VAS ;

Countries

China

Contacts

Public ContactWang Bo

Hefei Normal University

18756938320@163.com+86 187 5693 8320

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026