Wearable Electrogoniometry-Based Telerehabilitation After Total Knee Arthroplasty

NCT07779122 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 82

Last updated 2026-08-21

No results posted yet for this study

Summary

This study evaluated a wearable electrogoniometry-based telerehabilitation system designed to support recovery after total knee arthroplasty. Participants followed a home-based rehabilitation program, while patients in the intervention group additionally used a wearable knee device connected to a digital application that provided exercise guidance, real-time feedback, and remote monitoring. Knee range of motion, functional performance, and patient-reported outcomes were evaluated during postoperative recovery.

Conditions

Interventions

DEVICE

Wearable Electrogoniometry-Based Telerehabilitation System

Participants performed their prescribed postoperative rehabilitation exercises using the RebK wearable electrogoniometry-based telerehabilitation system. The wearable knee device was connected to a mobile application that guided exercise performance, provided real-time feedback on knee movement, and enabled remote monitoring of rehabilitation progress by the clinical team.

BEHAVIORAL

Standard Home-Based Rehabilitation Program

A standardized home-based exercise program following total knee arthroplasty, including therapeutic exercises aimed at improving knee range of motion, muscle strength, and functional recovery. Partici

Sponsors & Collaborators

  • University of Chile

    lead OTHER

Principal Investigators

  • Hachi Manzur, MD · University of Chile

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-05-31
Primary Completion
2024-09-12
Completion
2024-09-12

Countries

  • Chile

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07779122 on ClinicalTrials.gov