Usability and Reliability of a New Physical Therapy Tool

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 (n=20) 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 N/A 3. Blinding N/A 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 (e.g., 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.