Ireland
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Latest
Recruiting Not applicable

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

NCT06744218 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2024-11-22
Last updated
2025-12-26

Condition(s) studied

Rotator Cuff Injuries

Investigational drug(s) / intervention(s)

Standard TreatmentExperimental Treatment

Standard Treatment: Patients who will be assigned to the control group and subjected to standard treatment (usual care at our clinic) will undergo a physiotherapy treatment of 8 in-person sessions for 4 post-operative weeks

Experimental Treatment: patients who will be assigned to the experimental group and subjected to the experimental treatment will undergo a physiotherapy treatment of 8 sessions in telerehabilitation for 4 post-operative weeks

Study 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.

Eligibility

Sex
ALL
Min age
40 Years
Max age
70 Years
Healthy volunteers
No
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

Primary outcome measure(s)

  • Constant-Murley Score — 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

Trial sites (2)

FacilityCityRegionStatus
Ospedale del Delta Lagosanto Ferrara Not Yet Recruiting
IRCCS Istituto ortopedico Rizzoli Bologna Italia Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06744218 on ClinicalTrials.gov ↗ ← All trials in Italy