Trial Outcomes & Findings for Feasibility and Safety of Digital Rehab Platform for Bedridden Patients (NCT NCT06849765)
NCT ID: NCT06849765
Last Updated: 2026-04-17
Results Overview
Patient adherence was defined as the percentage of completed exercise time relative to the total prescribed exercise time.
COMPLETED
NA
25 participants
From enrollment to the end of treatment at 2 weeks
2026-04-17
Participant Flow
Participants were recruited from a single tertiary hospital and screened for eligibility based on the study inclusion and exclusion criteria.
All eligible participants were enrolled and assigned to a single intervention group without randomization.
Participant milestones
| Measure |
Digital Rehabilitation Program
Participants received a digital rehabilitation program delivered through a virtual reality-based rehabilitation platform.
|
|---|---|
|
Overall Study
STARTED
|
25
|
|
Overall Study
COMPLETED
|
20
|
|
Overall Study
NOT COMPLETED
|
5
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Race and Ethnicity were not collected from any participant.
Baseline characteristics by cohort
| Measure |
Digital Rehabilitation Program
n=25 Participants
Participants received a digital rehabilitation program delivered through a virtual reality-based rehabilitation platform.
|
|---|---|
|
Age, Continuous
|
53.08 years
STANDARD_DEVIATION 15.59 • n=25 Participants
|
|
Sex: Female, Male
Female
|
13 Participants
n=25 Participants
|
|
Sex: Female, Male
Male
|
12 Participants
n=25 Participants
|
PRIMARY outcome
Timeframe: From enrollment to the end of treatment at 2 weeksPatient adherence was defined as the percentage of completed exercise time relative to the total prescribed exercise time.
Outcome measures
| Measure |
Intervention
n=20 Participants
The rehabilitation program will utilize the MORA app to create individualized interventions based on each patient's physical capabilities.
|
|---|---|
|
Feasibility
|
75.3 percentage
Standard Deviation 12.4
|
SECONDARY outcome
Timeframe: From enrollment to the end of treatment at 2 weeksMonitoring the number of occurrences of adverse events such as pain, falls, dizziness, and any other negative reactions during the rehabilitation sessions.
Outcome measures
| Measure |
Intervention
n=20 Participants
The rehabilitation program will utilize the MORA app to create individualized interventions based on each patient's physical capabilities.
|
|---|---|
|
Number of Adverse Events
|
0 event
|
OTHER_PRE_SPECIFIED outcome
Timeframe: From enrollment to the end of treatment at 2 weeksSummation score of muscle strength based on MRC scale. Unit of Measure: Sum score (0 to 60, where a higher score indicates better overall muscle strength.)
Outcome measures
Outcome data not reported
OTHER_PRE_SPECIFIED outcome
Timeframe: From enrollment to the end of treatment at 2 weeksMeasurement of the level of ambulation and assistance required. Unit of Measure: FAC score (0 to 5, where a higher score indicates greater walking independence.)
Outcome measures
Outcome data not reported
OTHER_PRE_SPECIFIED outcome
Timeframe: From enrollment to the end of treatment at 2 weeksMeasurement of grip strength using a dynamometer. Unit of Measure: Force (kg) (A higher value indicates better grip strength.)
Outcome measures
Outcome data not reported
OTHER_PRE_SPECIFIED outcome
Timeframe: From enrollment to the end of treatment at 2 weeksAssessment of knee extensor strength using a dynamometer. Unit of Measure: Force (N or kg) (A higher value indicates stronger knee extensor muscles.)
Outcome measures
Outcome data not reported
OTHER_PRE_SPECIFIED outcome
Timeframe: From enrollment to the end of treatment at 2 weeksAssessment of walking speed and functional mobility over a 10-meter distance. Unit of Measure: Time (seconds) or speed (m/s) (For time: A lower value indicates faster walking ability. For speed: A higher value indicates better walking performance.)
Outcome measures
Outcome data not reported
OTHER_PRE_SPECIFIED outcome
Timeframe: From enrollment to the end of treatment at 2 weeksCognitive function assessment using the MMSE tool. Unit of Measure: MMSE score (0 to 30, where a higher score indicates better cognitive function.)
Outcome measures
Outcome data not reported
OTHER_PRE_SPECIFIED outcome
Timeframe: From enrollment to the end of treatment at 2 weeksAssessment of patient satisfaction with the MORA app and its use during rehabilitation exercises. Measurement Tool: Overall satisfaction, interest about health, Application-related questions, exercise intensity questionnaire (5-point Likert scale) Unit of Measure: Satisfaction score (1 to 5, where a higher score indicates greater satisfaction.)
Outcome measures
Outcome data not reported
OTHER_PRE_SPECIFIED outcome
Timeframe: From enrollment to the end of treatment at 2 weeksAssessment of patient-reported quality of life using the EQ-5D questionnaire, covering mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Unit of Measure: Utility score (0 to 1) and VAS score (0 to 100)
Outcome measures
Outcome data not reported
Adverse Events
Digital Rehabilitation Program
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place