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Knee Biofeedback Rehabilitation Through Game Therapy

Knee-Biofeedback Rehabilitation Interface for Game-based Home Therapy

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06090097
Acronym
KneeBRIGHT
Enrollment
60
Registered
2023-10-19
Start date
2024-09-04
Completion date
2026-11-30
Last updated
2025-12-03

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

Conditions

Knee Osteoarthritis

Keywords

knee osteoarthritis, physical therapy, rehabilitation

Brief summary

The goal of this study is to learn about the effect of video-game based rehabilitation exercise for patients with knee osteoarthritis. The main question the study aims to answer is: do patients who exercise with the game have better functional outcomes and engagement compared to patients who do conventional exercise? Participants will complete 10 weeks of physical therapy exercise sessions that focus on quadriceps strengthening. Two sessions per week will be conducted in the clinic, and one session will be conducted at home each week. The interventional group will conduct all exercises using the KneeBRIGHT EMG sensors and game software. The control group will conduct all exercises following a standard physical therapy regimen. Researchers will compare knee function and engagement between the group who uses the game, and the group who does conventional exercise.

Detailed description

The KneeBRIGHT game system will be evaluated in a 10-week single-blinded randomized controlled trial. The goals of this study are to: (1) assess improvements in functional outcomes following an exercise regimen conducted by KneeBRIGHT compared to conventional exercise; and (2) evaluate patient engagement during unsupervised, home-based exercises with and without the KneeBRIGHT software. Over the course of the study period, the knee OA participants will conduct physical therapy sessions with the physical therapist (PT) who enrolled them. The exercise regimen will implement each PT's standard of care, consisting of two weekly clinic sessions and one weekly home exercise session, for 10 weeks. Knee OA participants will be randomly assigned (via block randomization for each PT) to use either the KneeBRIGHT system for both clinic and home exercise, or to receive standard care with conventional exercise routines. Participants will conduct functional exercise assessments on study intake and again on study completion. Participants will also complete questionnaires focused on exercise engagement on study completion.

Interventions

DEVICEKneeBRIGHT System

The KneeBRIGHT system includes electromyogram sensors and video game software that leads participants through physical therapy exercise.

The control group will complete a 10-week regimen of conventional PT exercise

Sponsors

University of North Carolina, Chapel Hill
CollaboratorOTHER
Barron Associates, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Researchers conducting functional outcomes on study completion will be blinded from the intervention group.

Intervention model description

randomized control trial

Eligibility

Sex/Gender
ALL
Age
30 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* diagnosis via x-ray, with a score of at least 2 (out of 4) on the Kellgren-Lawrence OA scoring system; independent ambulation without assistive device

Exclusion criteria

* individuals who have psychiatric or cognitive impairment (e.g., dementia) that interferes with their ability to follow instructions or provide voluntary consent; symptomatic spine, hip, ankle, or foot disease other than OA that would interfere with assessment of the knee.

Design outcomes

Primary

MeasureTime frameDescription
Timed get-up-and-go scoreAfter 10 weeks (study completion)In the timed up and go (TUG) test, subjects are asked to rise from a standard armchair, walk to a marker 3 m away, turn, walk back, and sit down again.
Quadriceps strengthAfter 10 weeks (study completion)Quadriceps strength will be measured by recording isokinetic knee extension torque as measured by a dynamometer
Patient Activation Model ScoresAfter 10 weeks (study completion)The Patient Activation Model (PAM) is an established, highly reliable, questionnaire that reflects a developmental model of patient engagement with their healthcare regimens
Knee Osteoarthritis Outcome ScoreAfter 10 weeks (study completion)A multi-dimensional assessment that classifies knee outcomes into five categories: pain, symptoms, activities of daily living (ADL), sport, and quality of life
6-minute walk testAfter 10 weeks (study completion)The six-minute walk test (6MWT) measures the distance an individual is able to walk over a total of six minutes on a hard, flat surface.

Secondary

MeasureTime frameDescription
Patient technology acceptanceAfter 10 weeks (study completion)Participants will complete a questionnaire, designed based on the established Technology Acceptance Model to assess their level of technology acceptance.

Other

MeasureTime frameDescription
Patient home exercise adherenceAfter 10 weeks (study completion)The KneeBRIGHT software will log the exercises completed at home; these logs will report number of exercises conducted, level of resistance, and timestamps for the sessions. Control group participants will log home exercises using a written checklist of exercises

Countries

United States

Contacts

Primary ContactEileen Krepkovich, MS
krepkovich@barronassociates.com4349731215

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026