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Wearable Electrogoniometry-Based Telerehabilitation After Total Knee Arthroplasty

Sistema de telerrehabilitación Guiado Por electrogoniometría, lúdico y de Bajo Costo, Para la recuperación Funcional Posterior a Una Artroplastia de Rodilla en Personas Mayores

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07779122
Enrollment
82
Registered
2026-08-21
Start date
2022-05-31
Completion date
2024-09-12
Last updated
2026-08-21

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

Conditions

Knee Osteoarthritis, TKA

Keywords

Telerehabilitation, Electrogoniometry, Wearable Technology, Total Knee Arthroplasty, Postoperative Rehabilitation, Range of Motion

Brief 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.

Detailed description

Participants were allocated sequentially in a non-randomized manner. The first 50 enrolled participants constituted the control group, and the subsequent 32 participants were allocated to the intervention group and received the wearable electrogoniometry-based telerehabilitation system. All participants underwent a preoperative baseline assessment. Following total knee arthroplasty, participants were followed weekly during the first 8 postoperative weeks, with a final assessment at 12 weeks. Clinical and functional outcomes included knee range of motion, functional performance, and self-reported assessments. Participants in the intervention group additionally completed a questionnaire evaluating the usability of and their experience with the technology-assisted rehabilitation system.

Interventions

DEVICEWearable 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.

BEHAVIORALStandard 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

University of Chile
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Participants were assigned sequentially to two parallel groups in a non-randomized manner. The first 50 enrolled participants were assigned to the control group and received the standard home-based rehabilitation program. The subsequent 32 participants were assigned to the intervention group and received the same rehabilitation program supported by the wearable electrogoniometry-based telerehabilitation system.

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Adults older than 60 years. Scheduled for primary total knee arthroplasty for knee osteoarthritis. Able to attend weekly postoperative range-of-motion assessments.

Exclusion criteria

Revision arthroplasty. Use of constrained implants. Cognitive impairment preventing adherence to rehabilitation instructions. Inability to participate in follow-up assessments.

Design outcomes

Primary

MeasureTime frameDescription
Active Knee Flexion Range of MotionPreoperative baseline, weekly during postoperative weeks 1-8, and postoperative week 12Active knee flexion range of motion, measured in degrees using standardized goniometry. Higher values indicate greater knee flexion.
Passive Knee Flexion Range of MotionPreoperative baseline, weekly during postoperative weeks 1-8, and postoperative week 12Passive knee flexion range of motion, measured in degrees using standardized goniometry. Higher values indicate greater knee flexion.
Active Knee Extension Range of MotionPreoperative baseline, weekly during postoperative weeks 1-8, and postoperative week 12Active knee extension range of motion, measured in degrees using standardized goniometry. A value of 0° indicates full knee extension, while negative values indicate an extension deficit.
Passive Knee ExtensionPreoperative baseline, weekly during postoperative weeks 1-8, and postoperative week 12Passive knee extension range of motion, measured in degrees using standardized goniometry. A value of 0° indicates full knee extension, while negative values indicate an extension deficit.

Secondary

MeasureTime frameDescription
30-Second Sit-to-Stand TestPreoperative baseline, weekly during postoperative weeks 1-8, and postoperative week 12Functional performance assessed as the total number of complete sit-to-stand repetitions performed within 30 seconds. Higher values indicate better functional performance.
Usability of the Technology-Assisted Rehabilitation SystemPostoperative week 12Usability of the wearable electrogoniometry-based telerehabilitation system assessed using a structured patient questionnaire. Items were rated on a 5-point Likert scale, with higher scores indicating more favorable usability ratings.

Countries

Chile

Contacts

PRINCIPAL_INVESTIGATORHachi Manzur, MD

University of Chile

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 22, 2026