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Effects of exercise in a virtual reality (VR) space on motor and cognitive learning

Basic research on motor and cognitive learning using virtual reality - Basic research on motor and cognitive learning using virtual reality

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000045029
Enrollment
20
Registered
2021-09-01
Start date
2021-09-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Healthy adults between 20 and 80 years of age

Interventions

20 minutes of exercise task in the real world =&gt
1 week of washout period =&gt
20 minutes of exercise task in VR space =&gt
20 minutes of exercise task in VR space + tDCS. The VR device is a Leap Motion Controller (80mm x 30mm x 11mm) manufactured by Leap Motion. When the user moves his/her fingers in front of the sensor
20 minutes of exercise task in VR space + tDCS =&gt
20 minutes of exercise task in VR space. 20 minutes exercise task in VR space =&gt
1 week washout period =&gt
20 minutes exercise task in real world =&gt
20 minutes exercise task in VR space + tDCS. 20 minutes exercise task in VR space =&gt
20 minutes exercise task in VR space + tDCS =&gt
20 minutes exercise task in real world. 20 minutes of exercise task in VR space + tDCS =&gt

Sponsors

University of Fukui hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Those who have received sufficient explanations about participation in this study and have obtained the written consent of the subject of their own free will with full understanding.

Exclusion criteria

Exclusion criteria: Subjects who fall under any one of the following are excluded. (1) Subjects with a history of epilepsy (2) Do not have a history of central nervous system disease or motor system disease that causes functional impairment of the upper limbs. (3) Pregnant women, those who may be pregnant, or those who are breastfeeding. (4) Those who have participated in other clinical trials within the past 4 months. (5) Others who are judged by the principal investigator to be inappropriate as research subjects.

Design outcomes

Primary

MeasureTime frame
Box and Block Test (measurement of the number of blocks that can be carried in one minute) will be conducted before and after each intervention condition to examine the effectiveness.

Secondary

MeasureTime frame
Motor evoked potentials to evaluate the excitability of the corticospinal tract, cognitive tasks (Kohs block design test, Rey-Osterrieth Complex Figure Test, nasal finger-nose test, BIT (Behavioral Inattention Test) imitation task), and motor tasks (Simple Test for Evaluating Hand Function) will be conducted before and after each intervention condition.

Countries

Japan

Contacts

Public ContactHideaki Matsuo

University of Fukui hospital Division of Physical Therapy and Rehabilitation Medicine

hideakim@u-fukui.ac.jp0776613111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026