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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06744218
Enrollment
46
Registered
2024-12-20
Start date
2024-11-22
Completion date
2026-11-30
Last updated
2025-12-26

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

Conditions

Rotator Cuff Injuries

Keywords

telerehabilitation, physiotherapist, rotator cuff repair surgery

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.

Interventions

PROCEDUREStandard 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

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

Sponsors

Istituto Ortopedico Rizzoli
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 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

Design outcomes

Primary

MeasureTime frameDescription
Constant-Murley ScoreAt baseline (day 0), after one months, after 3 monthsThe 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

MeasureTime frameDescription
Mobility of the shoulderAt baseline (day 0), after one months, after 3 monthsRange of motion of the shoulder seen by movements made during the rehabilitation
Numeric rating scaleAt baseline (day 0), after one months, after 3 monthsDescription of pain by numeric rating scale, from 0 no pain, to 10 worst pain ever (0-10)
Disabilities of the Arm, Shoulder and Handat baseline, after 3 months and after 6 monthsThe Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire is a 30-item questionnaire that examines a patient's ability to perform certain upper extremity activities

Countries

Italy

Contacts

Primary ContactSilvana Sartini, MD
silvana.sartini@ior.it0516366

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026