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Weakness, MuscleYOOMINCT05815017

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

A study testing Yoomi Physical Therapy Software in people with Weakness, Muscle and Delirium in Old Age, run by Rutgers, The State University of New Jersey at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 65 years and olderHealthy volunteers can take part
What is being tested?
Yoomi Physical Therapy Software
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteUnited States
Study dates
29 Nov 2023to 1 Feb 2025
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 65 years and older
  • All sexes
  • Healthy volunteers accepted
  • Older adult

Who may be able to join

  • >= 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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Robert Wood Johnson University Hospital

    New Brunswick, New Jersey, 08901

Other trials in United States

About this study

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.

Being tested
Yoomi Physical Therapy Software
Keywords
Artificial Intelligence (AI), Physical Therapy, Hospitalization related muscle atrophy, Hospitalization associated decline, Inpatient rehabilitation, AI driven physical therapy
Medical subject headings
Muscle Weakness, Muscular Atrophy, Asthenia, Iatrogenic Disease, Sedentary Behavior

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Yoomi Physical Therapy SoftwareDevice

    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.

Study groups in NCT05815017
Study groupRoleWhat they receive
Gamified Physical Therapy Exercise Software Intervention + Usual CareExperimentalParticipants randomized to the intervention group will be asked each day by a volunteer whether they would like to use the gamified physical therapy exercise software while in their beds. Participants willing to exercise will have the device set up for them to participate by a volunteer and the software will begin with a tutorial video for different exercises 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.
Receives: Device: Yoomi Physical Therapy Software
Usual CareNo interventionUsual Care

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. % of Participants Who Reported "Yes" to Enjoying Their Work Out and Believing They Benefited From the Activity for Intervention Group Questionnaire.

    % 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.

    Measured: Collected daily at the end of each workout. Survey responses were averaged for each participant.

  2. Mean Software Utilization Time for Intervention Group (Change is Being Assessed)

    Mean 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.

    Measured: Collected daily throughout duration of patient hospitalization, usually 1-2 weeks, Daily minutes were averaged over sessions

  3. Average Exercise Repetitions Completed for Intervention Group

    Completed 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.

    Measured: Collected daily throughout duration of patient hospitalization, usually 1-2 weeks

Secondary outcomes (3)
  1. Average Change in Activity Measure for Post Acute Care (AMPAC) Scores

    Activity Measure for Post Acute Care (AMPAC) scores done by nurses twice daily (Score ranging from 0 to 24 with higher being better)

    Measured: Collected daily throughout duration of patient hospitalization, usually 1-2 weeks, Daily scores were averaged

  2. Length of Hospital Stay

    Measured: Collected at the time of discharge of patient hospitalization, usually 1-2 weeks

  3. Discharged Home

    Number of Participants with discharged home (as opposed to rehab, SNF)

    Measured: Collected at time of discharge, usually 1-2 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Apr 2023
  2. Study start29 Nov 2023
  3. Primary completion1 Feb 2025
  4. Study completion1 Feb 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05815017
Sponsor's protocol ID
Pro2022002225
Acronym
YOOMI
Status last verified
Aug 2026
First submitted
8 Mar 2023
Last updated
7 Aug 2026
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Yoomi Physical Therapy Software in people with Weakness, Muscle and Delirium in Old Age, run by Rutgers, The State University of New Jersey at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 7 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 7 Aug 2026). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

% of Participants Who Reported "Yes" to Enjoying Their Work Out and Believing They Benefited From the Activity for Intervention Group Questionnaire. (time frame: Collected daily at the end of each workout. Survey responses were averaged for each participant.). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Aug 2026.

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