Ignite Creation Date:
2024-05-06 @ 1:05 AM
Last Modification Date:
2024-10-26 @ 10:59 AM
Study NCT ID:
NCT01727856
Status:
COMPLETED
Last Update Posted:
2014-11-06
First Post:
2012-11-01
Brief Title:
Usability and Reliability of a New Physical Therapy Tool
Sponsor:
Reflexion Health Inc
Organization:
Reflexion Health Inc
Study Overview
Official Title:
An Evaluation of a Novel Motion Tracking Enabled Knee Physical Therapy Application With Healthy Patients to Assess Reliability and Usability
Status:
COMPLETED
Status Verified Date:
2014-11
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Rehabilitation exercise conducted at home following injury improves clinical and functional outcomes Optimum compliance with prescribed exercise regimens requires regular patient instruction performance assessment monitoring and general encouragement from healthcare staff Exercise at home though convenient for patients is not conducive for provision of the professional support needed to maximize prescribed regimen effectiveness
Software in development by Reflexion Health Inc along with the Naval Medical Center San Diego NMCSD is being designed to facilitate remote staff-patient interaction during at-home rehabilitative exercise sessions Microsoft Kinect will serve as the hardware platform for the designed software package tentatively called Reflexion Kinect contains a marker-lesscontroller-less motion tracking camera The final Reflexion software will rely on a Rehabilitation Measurement Tool RMT to detect cardinal plane skeletal joint movement and its velocity utilizing the embedded Kinect camera while also providing patient visual feedback via an avatar on a television screen
In this observational minimal risk study RMTKinect functional reliability and usability will be assessed Twenty healthy subjects will physically set-up and turn-on the hardwaresoftware system receive exercise directions from the RMT then conduct a series of knee exercises similar to those prescribed after anterior cruciate ligament ACL repair
An initial limited data set obtained by Reflexion Health provided validity and reliability measures Eighteen degrees of absolute difference was detected between manual goniometry and Kinect measurements in relevant planes of movement utilized during prescribed ACL exercise Good relative agreement between RMT and goniometry scores was obtained ICC 089 A correctable systematic bias toward underestimation by the RMT will allow for future more accurate estimations of joint positioning improving face validity
RMT functional reliability and general usability will be expressed in this study utilizing descriptive statistics and scaled questionnaires Hardware component malfunction Kinect camera laptop PC or LCD televisionmonitor as well as RMT internally logged software errors and failure will tallied and measured to ascertain RMT reliability
User-RMT interaction quality will be evaluated with video recordings of each set-up and exercise session Specifically usability measures will include need for additional assistance setting-up or operating the RMT number of attempts required by the subject to interact with a specific feature time spent on specific elements during the session Participant feedback will be elicited post-session using two scaled questionnaires System Usability Scale SUSand Reflexion Usability Scale RUS Findings from the study will guide software modifications needed prior to implementation of future clinical studies within the NMCSD population
Software in development by Reflexion Health Inc along with the Naval Medical Center San Diego NMCSD is being designed to facilitate remote staff-patient interaction during at-home rehabilitative exercise sessions Microsoft Kinect will serve as the hardware platform for the designed software package tentatively called Reflexion Kinect contains a marker-lesscontroller-less motion tracking camera The final Reflexion software will rely on a Rehabilitation Measurement Tool RMT to detect cardinal plane skeletal joint movement and its velocity utilizing the embedded Kinect camera while also providing patient visual feedback via an avatar on a television screen
In this observational minimal risk study RMTKinect functional reliability and usability will be assessed Twenty healthy subjects will physically set-up and turn-on the hardwaresoftware system receive exercise directions from the RMT then conduct a series of knee exercises similar to those prescribed after anterior cruciate ligament ACL repair
An initial limited data set obtained by Reflexion Health provided validity and reliability measures Eighteen degrees of absolute difference was detected between manual goniometry and Kinect measurements in relevant planes of movement utilized during prescribed ACL exercise Good relative agreement between RMT and goniometry scores was obtained ICC 089 A correctable systematic bias toward underestimation by the RMT will allow for future more accurate estimations of joint positioning improving face validity
RMT functional reliability and general usability will be expressed in this study utilizing descriptive statistics and scaled questionnaires Hardware component malfunction Kinect camera laptop PC or LCD televisionmonitor as well as RMT internally logged software errors and failure will tallied and measured to ascertain RMT reliability
User-RMT interaction quality will be evaluated with video recordings of each set-up and exercise session Specifically usability measures will include need for additional assistance setting-up or operating the RMT number of attempts required by the subject to interact with a specific feature time spent on specific elements during the session Participant feedback will be elicited post-session using two scaled questionnaires System Usability Scale SUSand Reflexion Usability Scale RUS Findings from the study will guide software modifications needed prior to implementation of future clinical studies within the NMCSD population
Detailed Description:
1 General Approach
We plan on using an observational study design to assess the reliability and usability of the RMT by healthy volunteers as they participate in a simulated session of knee physical therapy as presented by the RMT Each session will be supervised by research staff and recorded for later review and assessment of areas of concern for reliability and usability
2 Methods
The study will use 20 n20 healthy volunteers These subjects will be actively recruited from Naval Medical Center San Diego and Orthopedic by research staff We will also use an informational flyer placed in the NMCSD Physical Therapy and Orthopedic outpatient clinic waiting room No medical records will be used to identify subjects for recruitment Subjects will be approached by research staff and will be asked about participation and will undergo standard practices regarding meeting inclusion and exclusion criteria and clinical trial consent by trained research staff Those who consent to participate will be taken to an area that houses the RMT hardware and software Subjects will then undergo a brief 5 minute tutorial on the setup power-on and navigation of the hardware and gesture controlled software
After the orientation session each subject will be presented the RMT hardware and asked to connect the hardware components via provided cables and subsequently power on the system and application as well as position themselves correctly in front of the camera Next they will be instructed to follow the on screen prompts to enter their subject ID and pertinent login information and navigate the system using gestures Following the setup process they will then proceed to engage in four exercises sequentially presented by the RMT software Approximately 5 repetitions of each exercise will be recorded and evaluated by the RMT after which the subject will be asked to follow the onscreen prompts to review a summary of their activity as presented by the RMT and exit the application After their interaction with the RMT they will be asked to complete a System Usability Scale questionnaire as well as a Reflexion Usability Scale questionnaire
We anticipate the total time required by each subject will be approximately 45 minutes Research staff will be available to provide any assistance as requested by the subjects in their interaction with the RMT Additionally staff will also intervene while consented subjects perform the exercises if they detect any signs of impending injury or harm Subjects will be allowed to terminate their involvement at any time and for any reason
Review of the research staff notes during the subject interaction with the RMT SUS and RUS results and videotape of the interaction between the subject and RMT will be corroborated post-hoc
1 Sample Size
We estimate the sample size of this study to be approximately 20 subjects Since no direct comparison is being made to a control cohort no inferential statistical analysis will be performed This means that there is no meaningful way to appropriately power the study via sample size adjustments Our choice of 20 subjects therefore was based on balancing the logistics required to test this platform with collecting sufficient data to understand the usability of then system
2 Randomization
NA
3 Blinding
NA
4 Initial Orientation Session
Subjects will be given a brief video tutorial on how to connect the Kinect camera to the television and laptop power on the RMT and Kinect camera and operate the RMT hardware and software by research staff any questions will be answered at that time regarding RMT operation Then subjects will be evaluated by a licensed currently practicing physical therapist and shown the four exercises they will perform in the session The therapist will work with each of the patients until they achieve a satisfactory performance in each of the exercises as assessed by the therapist
3 Components
Hardware
Kinect Camera
LCD Television
Laptop PC
Software
Windows 7 Operating System
Rehabilitation Measurement Tool Software Application
4 Statistical Analysis
The primary goal of this research is to understand the usability and reliability of the system Since the present application is relatively novel there are no standard mthods to success or failure of the system Therefore we do not intend to perform any inferential statistical analyses Rather we will generate descriptive statistics to be used in a post-hoc fashion to determine system reliability and usability for future applications to sick patients undergoing physical therapy for post-ACL reconstruction surgery Descriptive statistics provide better insight into the data allowing a more informed assessment of potential risks of the system Understanding the distributional nature of the data eg normal symmetric normal skewed bimodal etc and the variability of the data scores can better identify overall safety risks as well as help to specify individuals that could potentially incur a greater safety risk should one exist
We plan on using an observational study design to assess the reliability and usability of the RMT by healthy volunteers as they participate in a simulated session of knee physical therapy as presented by the RMT Each session will be supervised by research staff and recorded for later review and assessment of areas of concern for reliability and usability
2 Methods
The study will use 20 n20 healthy volunteers These subjects will be actively recruited from Naval Medical Center San Diego and Orthopedic by research staff We will also use an informational flyer placed in the NMCSD Physical Therapy and Orthopedic outpatient clinic waiting room No medical records will be used to identify subjects for recruitment Subjects will be approached by research staff and will be asked about participation and will undergo standard practices regarding meeting inclusion and exclusion criteria and clinical trial consent by trained research staff Those who consent to participate will be taken to an area that houses the RMT hardware and software Subjects will then undergo a brief 5 minute tutorial on the setup power-on and navigation of the hardware and gesture controlled software
After the orientation session each subject will be presented the RMT hardware and asked to connect the hardware components via provided cables and subsequently power on the system and application as well as position themselves correctly in front of the camera Next they will be instructed to follow the on screen prompts to enter their subject ID and pertinent login information and navigate the system using gestures Following the setup process they will then proceed to engage in four exercises sequentially presented by the RMT software Approximately 5 repetitions of each exercise will be recorded and evaluated by the RMT after which the subject will be asked to follow the onscreen prompts to review a summary of their activity as presented by the RMT and exit the application After their interaction with the RMT they will be asked to complete a System Usability Scale questionnaire as well as a Reflexion Usability Scale questionnaire
We anticipate the total time required by each subject will be approximately 45 minutes Research staff will be available to provide any assistance as requested by the subjects in their interaction with the RMT Additionally staff will also intervene while consented subjects perform the exercises if they detect any signs of impending injury or harm Subjects will be allowed to terminate their involvement at any time and for any reason
Review of the research staff notes during the subject interaction with the RMT SUS and RUS results and videotape of the interaction between the subject and RMT will be corroborated post-hoc
1 Sample Size
We estimate the sample size of this study to be approximately 20 subjects Since no direct comparison is being made to a control cohort no inferential statistical analysis will be performed This means that there is no meaningful way to appropriately power the study via sample size adjustments Our choice of 20 subjects therefore was based on balancing the logistics required to test this platform with collecting sufficient data to understand the usability of then system
2 Randomization
NA
3 Blinding
NA
4 Initial Orientation Session
Subjects will be given a brief video tutorial on how to connect the Kinect camera to the television and laptop power on the RMT and Kinect camera and operate the RMT hardware and software by research staff any questions will be answered at that time regarding RMT operation Then subjects will be evaluated by a licensed currently practicing physical therapist and shown the four exercises they will perform in the session The therapist will work with each of the patients until they achieve a satisfactory performance in each of the exercises as assessed by the therapist
3 Components
Hardware
Kinect Camera
LCD Television
Laptop PC
Software
Windows 7 Operating System
Rehabilitation Measurement Tool Software Application
4 Statistical Analysis
The primary goal of this research is to understand the usability and reliability of the system Since the present application is relatively novel there are no standard mthods to success or failure of the system Therefore we do not intend to perform any inferential statistical analyses Rather we will generate descriptive statistics to be used in a post-hoc fashion to determine system reliability and usability for future applications to sick patients undergoing physical therapy for post-ACL reconstruction surgery Descriptive statistics provide better insight into the data allowing a more informed assessment of potential risks of the system Understanding the distributional nature of the data eg normal symmetric normal skewed bimodal etc and the variability of the data scores can better identify overall safety risks as well as help to specify individuals that could potentially incur a greater safety risk should one exist
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| NIH CTSA 8KL2TR000110-05 | OTHER_GRANT | NIH CTSA 8KL2TR000110-05 | None |