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A randomized controlled trial of different training methods to promote rehabilitation after rotator cuff repair surgery

A randomized controlled trial of different training methods to promote rehabilitation after rotator cuff repair surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077029
Enrollment
Unknown
Registered
2023-10-26
Start date
2023-10-31
Completion date
Unknown
Last updated
2023-10-30

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

Conditions

rotator cuff injury

Interventions

treatment group:Three times a day, each 20 minutes of training time, training movements for the passive forearm flexion holding the head
shrug the shoulders
passive climbing table training each 10 ~ 15 each time, each movement of the training process of the patient s subjective pain perception of the VAS score of no more than 3 points
control group:The control group underwent postoperative passive forearm flexion head-holding in sitting or standing position and passive forward flexion training in standing position lasting for one m

Sponsors

Renji Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: Preoperative diagnosis meets the diagnostic criteria for supraspinatus tears established by the American Academy of Orthopaedic Surgeons; initial arthroscopic shoulder repair; gender-neutral, 30 years = age = 80 years; preoperative shoulder pain of no more than one year; preoperative shoulder mobility =50% of normal; understanding of the purpose of the study and signing the informed consent form

Exclusion criteria

Exclusion criteria: Preoperative other serious organic pathologies or other diseases that can cause pain and anxiety; postoperative complications of more serious infections or deep vein thrombosis; patients with visual, hearing, or cognitive impairments; psychiatric illnesses

Design outcomes

Primary

MeasureTime frame
range motion of shoulder;Constant-Murley Score for the Shoulder Joint;VAS score;Measurement of periarticular shoulder pressure pain threshold;

Secondary

MeasureTime frame
Postoperative patient satisfaction survey;

Countries

China

Contacts

Public ContactYang Chunxi

Renji Hospital, Shanghai Jiao Tong University School of Medicine

yngchunxi@renji.com+86 186 0171 8996

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026