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The Effect of Virtual Reality (VR)-Based Exercise Intervention in Patients with Parkinson's Disease: A Multicenter Randomized Controlled Trial Utilizing the Eleven Table Tennis Game

The Effect of Virtual Reality (VR)-Based Exercise Intervention in Patients with Parkinson's Disease: A Multicenter Randomized Controlled Trial Utilizing the Eleven Table Tennis Game

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0010536
Enrollment
30
Registered
2025-05-26
Start date
2025-01-21
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

None listed

Interventions

Others(VR-based table tennis exercise intervention) : In this study, we compare a table tennis-based virtual reality (VR) exercise program with home-based training for patients with Parkinson’s diseas

Sponsors

Inje University Haeundae Paik Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with a confirmed diagnosis of Parkinson’s disease based on the clinical diagnostic criteria of the Movement Disorder Society (MDS) 2. Classified as Hoehn and Yahr stages 1–3, and capable of independent ambulation

Exclusion criteria

Exclusion criteria: 1. Patients diagnosed with dementia or severe depression (MoCA = 24) and currently under treatment 2. Patients with orthopedic conditions, such as arthritis or spinal disorders 3. Patients with a history of stroke or peripheral nerve and muscle disorders 4. Patients with severe visual or hearing impairments that prohibit the use of a VR headset 5. Patients deemed by the investigator to be at high risk of falls during VR-based table tennis exercises 6. Patients exhibiting moderate or higher levels of motion sickness symptoms on the Virtual Reality Sickness Questionnaire (VRSQ)

Design outcomes

Primary

MeasureTime frame
The primary outcome variable will be assessed using the Movement Disorder Society–Unified Parkinson’s Disease Rating Scale Part 3 (MDS-UPDRS Part 3). Changes in motor symptom scores before and after the intervention will be measured to evaluate the effectiveness of the intervention.

Secondary

MeasureTime frame
The secondary outcome variable will be measured using MDS-UPDRS Part 2, which evaluates changes in activities of daily living. Pre- and post-intervention score differences will be analyzed to assess the intervention's impact on patients’ functional abilities in daily life.;The secondary outcome variable will be measured using MDS-UPDRS Part 4, which evaluates complications of therapy, including dyskinesias and motor fluctuations. Differences between pre- and post-intervention scores will be analyzed to assess the impact of the intervention on treatment-related side effects.;Parkinson’s Disease Questionnaire-8 (PDQ-8) will be administered to assess changes in health-related quality of life. Pre- and post-intervention total scores will be compared to evaluate the impact of the intervention on patients’ perceived quality of life.;Timed Up and Go test (TUG) will be used to measure changes in gait and functional mobility. The time required for the patient to stand up from a chair, walk 3 meters, turn around, return, and sit down will be recorded. Differences between pre- and post-intervention times will be analyzed to assess improvements in mobility.

Countries

Korea, Republic of

Contacts

Public Contactsoohyun Lim

Inje University Haeundae Paik Hospital

haepaikneucrc@naver.com+82-51-797-0483

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026