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Clinical Trials/NCT06744218
NCT06744218
Recruiting
N/A

Effectiveness of Telerehabilitation as an Alternative to Outpatient Physiotherapy in the 1 Month After Arthroscopic Rotator Cuff Repair Surgery: Multicenter Randomized Clinical Trial

Istituto Ortopedico Rizzoli2 sites in 1 country46 target enrollmentNovember 22, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Rotator Cuff Injuries
Sponsor
Istituto Ortopedico Rizzoli
Enrollment
46
Locations
2
Primary Endpoint
Constant-Murley Score
Status
Recruiting
Last Updated
4 months ago

Overview

Brief Summary

The present study aims to verify whether telerehabilitation as an alternative to in-person treatment (both conducted by a physiotherapist) can be a valid option in terms of pain, recovery of the rom, shoulder functionality compared to those provided by therapy alone. face-to-face rehabilitation in patients undergoing arthroscopic rotator cuff repair surgery.

Registry
clinicaltrials.gov
Start Date
November 22, 2024
End Date
November 1, 2026
Last Updated
4 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male or female patients aged between 40 and 70 years
  • Patients undergoing arthroscopic repair surgery of the rotator cuff tendons
  • Start of outpatient treatment within 7 days of discharge from the Orthopedic Department of the Argenta and Delta hospitals
  • Continuation of rehabilitation care at the IOR Physical and Rehabilitation Medicine service in Argenta or at the Physical Therapy Rehabilitation Medicine service of the Delta Hospital.
  • Patients who have provided informed consent

Exclusion Criteria

  • Previous shoulder surgeries
  • difficulty understanding the Italian language/language barrier
  • unavailability of IT devices or stable wi-fi connection by the patient

Outcomes

Primary Outcomes

Constant-Murley Score

Time Frame: At baseline (day 0), after one months, after 3 months

The Constant-Murley score (CMS) is a 100-point scale made up of a series of individual parameters. These parameters define the patient's pain level and ability to carry out normal daily activities

Secondary Outcomes

  • Mobility of the shoulder(At baseline (day 0), after one months, after 3 months)
  • Numeric rating scale(At baseline (day 0), after one months, after 3 months)
  • Disabilities of the Arm, Shoulder and Hand(at baseline, after 3 months and after 6 months)

Study Sites (2)

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