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YOOMI: Effect of Gamified Physical Therapy Exercise Software on Inpatient Mobility

YOOMI: Effect of Gamified Physical Therapy Exercise Software on Inpatient Mobility

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05815017
Acronym
YOOMI
Enrollment
30
Registered
2023-04-18
Start date
2023-11-29
Completion date
2025-02-01
Last updated
2026-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delirium in Old Age, Hospital Acquired Condition, Muscle Atrophy or Weakness, Muscle Loss, Physical Disability, Physical Inactivity, Weakness, Muscle

Keywords

Artificial Intelligence (AI), Physical Therapy, Hospitalization related muscle atrophy, Hospitalization associated decline, Inpatient rehabilitation, AI driven physical therapy

Brief summary

Patients admitted to the hospital often develop functional impairments due to being in bed most of the day. Each day of bedrest leads to significant muscle loss. As a result, many patients become dependent on others or require rehabilitation at a facility to improve mobility and function prior to returning home. Staff in the hospital is limited and often unable to mobilize patients every day while hospitalized. The investigators are testing a new experimental gamified physical therapy exercise software to see if it can be a fun, enjoyable way to help mobilize patients without the assistance of staff. The primary aim of this pilot/proof of concept study is to determine whether gamified physical therapy software can help inpatients exercise within the safety of their own beds and preserve pre-hospitalization function.

Interventions

DEVICEYoomi Physical Therapy Software

Physical Therapy software via a computer/monitor will be set up for the patient. It will begin with a tutorial video for different exercises in the form of games and then ask patients to perform in sequence with prompting and motion tracking. Exercises include Frontal Bicep Curls, Arm Crosses, Press Ups, Arm Rotations, and Basketball Shots.

Sponsors

Rutgers, The State University of New Jersey
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* \>= 65 years of age * English-fluency in reading and speaking * Capacity to consent * Enrolled in HELP program * Attending physician confirms there are no medical contraindications to in-bed exercises

Exclusion criteria

* Unstable Psychiatric Illness * Unstable/Critically Ill Patients requiring ICU-level of care * Surgical tube present (e.g. JP drains) * Surgery during the hospitalization * Bed Rest Activity Order

Design outcomes

Primary

MeasureTime frameDescription
% of Participants Who Reported "Yes" to Enjoying Their Work Out and Believing They Benefited From the Activity for Intervention Group Questionnaire.Collected daily at the end of each workout. Survey responses were averaged for each participant.% Of participants who reported "yes" to enjoying their work out and believed they benefited from the activity. These are two questions from the survey that were combined. Scale includes "Yes", "Maybe", "No" as possible responses.
Mean Software Utilization Time for Intervention Group (Change is Being Assessed)Collected daily throughout duration of patient hospitalization, usually 1-2 weeks, Daily minutes were averaged over sessionsMean Software Utilization Time for Intervention Group was calculated by taking the mean of daily minutes per exercise session per participant, and then calculating the mean minutes utilization time for all participants.
Average Exercise Repetitions Completed for Intervention GroupCollected daily throughout duration of patient hospitalization, usually 1-2 weeksCompleted exercise repetitions per patient were calculated by taking the mean of each participant's daily exercise repetitions and then calculating a mean of all participants.

Secondary

MeasureTime frameDescription
Average Change in Activity Measure for Post Acute Care (AMPAC) ScoresCollected daily throughout duration of patient hospitalization, usually 1-2 weeks, Daily scores were averagedActivity Measure for Post Acute Care (AMPAC) scores done by nurses twice daily (Score ranging from 0 to 24 with higher being better)
Length of Hospital StayCollected at the time of discharge of patient hospitalization, usually 1-2 weeks
Discharged HomeCollected at time of discharge, usually 1-2 weeksNumber of Participants with discharged home (as opposed to rehab, SNF)

Countries

United States

Baseline characteristics

Characteristic
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
24 Participants
Age, Categorical
Between 18 and 65 years
0 Participants
Age, Continuous77.1 years
STANDARD_DEVIATION 6.6
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
0 Participants
Race (NIH/OMB)
Black or African American
2 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
White
20 Participants
Region of Enrollment
United States
14 participants
Sex: Female, Male
Female
5 Participants
Sex: Female, Male
Male
8 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 100 / 14
other
Total, other adverse events
0 / 100 / 14
serious
Total, serious adverse events
0 / 100 / 14

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 8, 2026