Actively Recruiting

Phase Not Applicable
Age: 40Years - 70Years
All Genders
NCT06744218

Effectiveness of Telerehabilitation as an Alternative to Outpatient Physiotherapy in the 1 Month After Arthroscopic Rotator Cuff Repair Surgery

Led by Istituto Ortopedico Rizzoli · Updated on 2025-12-26

46

Participants Needed

2

Research Sites

101 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Effectiveness of Telerehabilitation as an Alternative to Outpatient Physiotherapy in the 1 Month After Arthroscopic Rotator Cuff Repair Surgery

Who Can Participate

Age: 40Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

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

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Ospedale del Delta

Lagosanto, Ferrara, Italy, 44023

Not Yet Recruiting

2

IRCCS Istituto ortopedico Rizzoli

Bologna, Italia, Italy, 40136

Actively Recruiting

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Research Team

S

Silvana Sartini, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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