Measuring Postoperative Mobility, Gait Symmetry and Feedback Following TJA

NCT ID: NCT03673293

Last Updated: 2025-11-20

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 58 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2018-05-05
• Study Completion Date: 2025-08-08

Brief Summary

The objectives of this study are:

1. The investigators plan to evaluate and validate the use of a novel wireless insole device (Loadsol) that provides real-time biofeedback on post-operative mobility and weight bearing following total joint arthroplasty.

2. The investigators plan to utilize the wireless insole device to determine if biofeedback is sufficient for improving gait symmetry following total joint arthroplasty.

3. The investigators plan to determine if there is a correlation between patient reported outcomes and measured postoperative weight bearing.

Detailed Description

In orthopaedic and trauma surgery post-operative mobility is very important. Six-month mortality and patient satisfaction has been associated with mobility. Elderly patients may suffer from severe complications caused by immobility due to a high prevalence of comorbidities.

Measuring postoperative mobility has primarily been based on advanced technology and complicated gait laboratories (treadmill, force plate, videoanalysis). The recent introduction of mobile insole force devices, such as the pedoped loadsol® (Novel) may allow for a cost-effective and clinically relevant use of providing biofeedback.

Using video analysis to evaluate the insole device will allow for measurements in realistic situations like walking stairs, stand up from a chair, sit down, turning and walking. The investigators had previously completed this in the lab setting and further the feedback mode of the loadsol will be used for training the patients in terms of symmetry after a total knee replacement.

This study may have an important influence on the aftercare of the investigators patients. Determining the postoperative mobility and evaluating gait analysis in real time will allow the investigators to compare between different operative approaches, operative techniques, Implants and more. If the feedback mode is working as expected the investigators might use it in the close future in the investigators standard aftercare for all patients.

Conditions

Total Joint Arthroplasty

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• Planned or recently underwent (up to 8 weeks postoperatively) primary total joint arthroplasty
• Free walking before surgery, no devices needed
• Age >/=18 years
• Preoperative outcomes scores (PF CAT, PROMIS Global Health, KOOS JR)
• Written informed consent

Exclusion Criteria

• Index procedure is a revision total joint arthroplasty
• Total knee or hip arthroplasty on the contralateral side within 1 one year of index procedure
• Severe medical comorbidity (ASA>/=3)
• Participant is planning TJA on another joint within next 12 months
• Significant symptoms on contralateral knee/hip/ankle that could impede performance on study

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Utah

OTHER

Sponsor Role: lead

Responsible Party

Christopher Pelt

Principle Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Christopher Pelt, MD

Role: PRINCIPAL_INVESTIGATOR

University of Utah

Locations

University of Utah Orthopaedic Center

Salt Lake City, Utah, United States

Countries

United States

Other Identifiers

110935

Identifier Type: -

Identifier Source: org_study_id