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Interactive Virtual Telerehabilitation After Total Knee Arthroplasty (REHABITIC)

P

Parc de Salut Mar

Status

Completed

Conditions

Knee Osteoarthritis

Treatments

Other: Interactive Virtual Telerehabilitation (IVT)
Other: Standard care rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT01604174
REHABITIC

Details and patient eligibility

About

The purpose of this clinical trial is to compare the effectiveness of a new interactive virtual telerehabilitation (IVT) system with the conventional program in the rehabilitation of patients after total knee arthroplasty.

Full description

Patients are distributed into two treatment groups: 1) Group I (control): standard clinical protocol of TKA rehabilitation consisting of 1-hour sessions for 10 days; and 2) Group II (IVT): 1-hour IVT sessions for 10 days (5 sessions under a therapist's supervision to verify the absence of medical complications + 5 sessions performed at home). The IVT is an interactive virtual software-hardware platform that facilitates the development of remote rehabilitation therapy for multiple diseases. Patients receive information required to perform exercise and the therapist remotely monitors the patient's performance. For the purpose of this trial, the IVT system was designed for lower limb motor recovery in patients undergoing TKA.

Enrollment

140 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Post-TKA active range of motion: flexion 80º and extension -10º
  • ABsence of stiffness
  • Ability to walk with the use of a walking aid
  • Ability to read and understand Spanish
  • Ability to understand and accept the trial procedures and to sign an informed consent form in accordance with national legislation

Exclusion criteria

  • Sensory, cognitive and/or praxic impairment
  • Concomitant medical conditions that may influence the rehabilitation process
  • Discharge destination other than home
  • Patients with any local or systemic complication (e.g., surgical wound infection, suspicion of deep vein thrombosis...) in the three-month follow-up period

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

140 participants in 2 patient groups

Interactive Virtual Telerehabilitation
Experimental group
Description:
Rehabilitation by IVT
Treatment:
Other: Interactive Virtual Telerehabilitation (IVT)
Standard rehabilitation care
Active Comparator group
Description:
Standard care rehabilitation after total knee arthroplasty
Treatment:
Other: Standard care rehabilitation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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