Actively Recruiting

Phase Not Applicable
Age: 19Years +
All Genders
NCT06937463

Feasibility of Virtual Reality-Based Rehabilitation in Patients With Limited Mobility

Led by Asan Medical Center · Updated on 2025-04-25

28

Participants Needed

1

Research Sites

22 weeks

Total Duration

On this page

Sponsors

A

Asan Medical Center

Lead Sponsor

U

UNIST (Ulsan National Institute of Science and Technology)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Study title: Customized Evidence-Based Motion Recognition Rehabilitation Exercise System for Bed Stabilization Patients the purpose of the study This study aims to evaluate the effectiveness of rehabilitation programs using motion recognition-based games for patients who are bedridden in hospital settings. The main purpose of the study is to determine whether digital rehabilitation can substantially contribute to the improvement and recovery of physical function in patients with limited physical functioning. a study participant The study involved 28 adult patients who were hospitalized while lying in bed at a hospital. Participants use Nintendo Ring Fit, which provides a motion-aware-based game rehabilitation exercise program, and a personalized exercise plan is provided for each patient's physical condition. research methodology Exercise Protocol: Participants will perform a personalized exercise program for two weeks through Nintendo Ring Fit. The exercise lasts about 30 minutes, once a day and is supported by a therapist. Exercise intensity and type are adjusted to suit the patient's physical condition so that they proceed safely. Monitoring safety and effectiveness: Keep track of participants' physical functions (e.g., strength, mobility, etc.) during the study, and constantly monitor for any inconveniences or side effects that may occur during exercise sessions. This closely checks patients' motor responses and ensures safety. the duration of the study The study runs from September 2024 to December 2025, during which participants will undergo rehabilitation exercises using motion recognition-based games. Estimated results The study is expected to demonstrate that digital rehabilitation programs can be a safe and effective treatment option for patients who are bedridden in hospital settings. In addition, the findings will contribute to improving in-hospital rehabilitation practices and promoting physical recovery. Safety Considerations All exercises conducted in this study are designed with safety as the top priority, and exercise intensity is adjusted to low intensity. If patients experience discomfort or side effects during the exercise, they are monitored closely and allowed to take the necessary action immediately. All exercises are conducted safely under the supervision of a medical professional.

CONDITIONS

Official Title

Feasibility of Virtual Reality-Based Rehabilitation in Patients With Limited Mobility

Who Can Participate

Age: 19Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with restricted mobility (Functional Ambulation Category score of 3 or less) among those hospitalized for acute or surgical conditions
  • A Functional Ambulation Category score of 3 means one guardian is required to supervise walking without physical contact
  • Adults aged 19 years or older
  • Patients who have agreed to participate in the study
Not Eligible

You will not qualify if you...

  • Unable to cooperate in rehabilitation exercise programs due to low consciousness or cognitive impairment
  • Persistent biological instability
  • Severe muscle weakness, limited joint range of motion, amputation, or similar disabilities preventing exercise
  • Need to limit movement due to fracture or skeletal instability
  • Poor vision or hearing that prevents cooperation with the exercise program
  • Patients on mechanical ventilation for 24 hours or more

AI-Screening

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Trial Site Locations

Total: 1 location

1

Asan Medical Center

Songpa-gu, Seoul, South Korea, 05505

Actively Recruiting

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Research Team

W

won Kim (Associate professor), PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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