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.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

25 participants

Primary outcome timeframe

From enrollment to the end of treatment at 2 weeks

Results posted on

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

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

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 weeks

Patient adherence was defined as the percentage of completed exercise time relative to the total prescribed exercise time.

Outcome measures

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 weeks

Monitoring the number of occurrences of adverse events such as pain, falls, dizziness, and any other negative reactions during the rehabilitation sessions.

Outcome measures

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 weeks

Summation 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 weeks

Measurement 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 weeks

Measurement 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 weeks

Assessment 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 weeks

Assessment 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 weeks

Cognitive 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 weeks

Assessment 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 weeks

Assessment 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 events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Won Kim, MD, PhD

Asan Medical Center

Phone: 02-3010-3769

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place