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Knee Biofeedback Rehabilitation Through Game Therapy (KneeBRIGHT)

Primary Purpose

Knee Osteoarthritis

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
KneeBRIGHT System
Control Exercise
Sponsored by
Barron Associates, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Osteoarthritis focused on measuring knee osteoarthritis, physical therapy, rehabilitation

Eligibility Criteria

30 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • University of North Carolina Chapel Hill

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

KneeBRIGHT Group

Control Group

Arm Description

The interventional group will conduct all exercises during the 10-week therapy regimen using the KneeBRIGHT electromyogram sensors and game software.

The control group will conduct all exercises following a standard physical therapy regimen.

Outcomes

Primary Outcome Measures

Knee Osteoarthritis Outcome Score
A multi-dimensional assessment that classifies knee outcomes into five categories: pain, symptoms, activities of daily living (ADL), sport, and quality of life
Timed get-up-and-go score
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.
6-minute walk test
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.
Quadriceps strength
Quadriceps strength will be measured by recording isokinetic knee extension torque as measured by a dynamometer
Patient Activation Model Scores
The Patient Activation Model (PAM) is an established, highly reliable, questionnaire that reflects a developmental model of patient engagement with their healthcare regimens

Secondary Outcome Measures

Patient technology acceptance
Participants will complete a questionnaire, designed based on the established Technology Acceptance Model to assess their level of technology acceptance.

Full Information

First Posted
October 13, 2023
Last Updated
October 13, 2023
Sponsor
Barron Associates, Inc.
Collaborators
University of North Carolina, Chapel Hill
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1. Study Identification

Unique Protocol Identification Number
NCT06090097
Brief Title
Knee Biofeedback Rehabilitation Through Game Therapy
Acronym
KneeBRIGHT
Official Title
Knee-Biofeedback Rehabilitation Interface for Game-based Home Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 2024 (Anticipated)
Primary Completion Date
November 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Barron Associates, Inc.
Collaborators
University of North Carolina, Chapel Hill

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
Keywords
knee osteoarthritis, physical therapy, rehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
randomized control trial
Masking
Outcomes Assessor
Masking Description
Researchers conducting functional outcomes on study completion will be blinded from the intervention group.
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
KneeBRIGHT Group
Arm Type
Experimental
Arm Description
The interventional group will conduct all exercises during the 10-week therapy regimen using the KneeBRIGHT electromyogram sensors and game software.
Arm Title
Control Group
Arm Type
Active Comparator
Arm Description
The control group will conduct all exercises following a standard physical therapy regimen.
Intervention Type
Device
Intervention Name(s)
KneeBRIGHT System
Intervention Description
The KneeBRIGHT system includes electromyogram sensors and video game software that leads participants through physical therapy exercise.
Intervention Type
Other
Intervention Name(s)
Control Exercise
Intervention Description
The control group will complete a 10-week regimen of conventional PT exercise
Primary Outcome Measure Information:
Title
Knee Osteoarthritis Outcome Score
Description
A multi-dimensional assessment that classifies knee outcomes into five categories: pain, symptoms, activities of daily living (ADL), sport, and quality of life
Time Frame
After 10 weeks (study completion)
Title
Timed get-up-and-go score
Description
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.
Time Frame
After 10 weeks (study completion)
Title
6-minute walk test
Description
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.
Time Frame
After 10 weeks (study completion)
Title
Quadriceps strength
Description
Quadriceps strength will be measured by recording isokinetic knee extension torque as measured by a dynamometer
Time Frame
After 10 weeks (study completion)
Title
Patient Activation Model Scores
Description
The Patient Activation Model (PAM) is an established, highly reliable, questionnaire that reflects a developmental model of patient engagement with their healthcare regimens
Time Frame
After 10 weeks (study completion)
Secondary Outcome Measure Information:
Title
Patient technology acceptance
Description
Participants will complete a questionnaire, designed based on the established Technology Acceptance Model to assess their level of technology acceptance.
Time Frame
After 10 weeks (study completion)
Other Pre-specified Outcome Measures:
Title
Patient home exercise adherence
Description
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
Time Frame
After 10 weeks (study completion)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Eileen Krepkovich, MS
Phone
4349731215
Ext
123
Email
krepkovich@barronassociates.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eileen Krepkovich, MS
Organizational Affiliation
Barron Associates
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of North Carolina Chapel Hill
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joe M Hart, PhD
Phone
919-966-9166
Email
joe_hart@med.unc.edu
First Name & Middle Initial & Last Name & Degree
Joe M Hart, PhD
First Name & Middle Initial & Last Name & Degree
Carla Hill, DPT

12. IPD Sharing Statement

Plan to Share IPD
No

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Knee Biofeedback Rehabilitation Through Game Therapy

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