The objective of this study is to evaluate the feasibility of the MoveMend Health software program as an integrated supplement to traditional acute care/in-hospital occupational therapy for patients following liver and kidney transplants, as determined by recruitment rates, program completion, intervention adherence, safety incidence, and patient feedback on device/program performance.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Enrollment
12
Software-based therapeutic tool that offers gamified exercises and activities. The device is designed for deployment on tablets. The core purpose of the device is to augment patient engagement and participation in their own rehabilitation by providing additional therapeutic interventions between formal occupational therapy sessions.
NYU Langone Health
New York, New York, United States
Recruitment Rate
Calculated by dividing the number of participants enrolled by the total number of patients contacted or screened.
Time frame: Up to Month 6 Post-Operation
Percentage of Participants who Complete Exercise Program
Percentage of enrolled participants who complete the interventional program.
Time frame: Up to Month 6 Post-Operation
Percentage of Participants who Adhere to Intervention
Measured by session duration and frequency, as recorded by the device. Participants will be classified as "adhering" or "not adhering."
Time frame: Up to Month 6 Post-Operation
Number of Adverse Events
Measured using data from participant's electronic medical record.
Time frame: Up to Month 6 Post-Operation
Change in Activity Measure for Post-Acute Care (AMPAC) Score
12-item assessment of basic mobility of inpatients. Each item is rated on a Likert scale from 1-4. The raw score is the sum of responses, which is converted to a T-score. The total score is a T-score ranging from 0 to 100; higher scores indicate greater mobility.
Time frame: Baseline, End of Hospital Stay (typically no more than 6 months post-operation)
Change in Grip Strength
Measured as the percentage change in grip strength between the baseline assessment and the final assessment at discharge.
Time frame: Baseline, End of Hospital Stay (typically no more than 6 months post-operation)
Upper Extremity Range of Motion (ROM) Change
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Measured as the change in degrees of ROM at the shoulder and elbow as measured by a goniometer from baseline to discharge.
Time frame: Baseline, End of Hospital Stay (typically no more than 6 months post-operation)
Change in EuroQol 5-Dimension 5-Level (EQ-5D-5L) Questionnaire Index Score
The EQ-5D-5L is a self-reported health status questionnaire that consists of six questions used to calculate a health utility score for use in health economic analysis. There are two components to the EQ-5D-5L: a five-item health state profile that assesses mobility, self-care, usual activities, pain/discomfort, and anxiety/depression used to obtain an Index Utility Score, as well as a visual analogue scale (VAS) that measures health state. Overall scores range from 0 to 1, with low scores representing a higher level of dysfunction.
Time frame: Baseline, End of Hospital Stay (typically no more than 6 months post-operation)