Compliance With PROMs Detection Through Digital Support and Correlation Compared Standard to Outpatient Detection in Knee Prosthetics

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-78
SponsorIstituto Ortopedico Rizzoli

About this trial

Two methods for detecting outcomes after knee prosthetic surgery are compared: the traditional one using paper questionnaires administered in the outpatient setting (Oxford Knee Score) VS detection using digital questionnaires created on Google Forms and sent to the patient's smartphone on which the compilation takes place in the extra area outpatient.

Eligibility criteria

Qualifiers

patients with gonarthrosis with indication of hip arthroplasty

males and females aged 18-78 and with a Barthel scale score ≥ 91

patients in possession of private digital electronic support (smartphone, tablet or PC)

Disqualifiers

patients with a Barthel scale score ≤ 90

patients with psychiatric pathologies, a history of drug and alcohol abuse

patients not in possession of private digital electronic support

Trial design

Treatments tested in this trial

  • Extrambulatory digital PROMs detection

Treatment groups

50 Participants
are divided into 1 treatment group

Sponsors and collaborators