Could VR worlds sharpen the aging mind? a new trial puts it to the test
NCT ID NCT07033468
First seen Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time
Summary
This study tests whether fully immersive virtual reality (VR) cognitive training can improve thinking skills in people with mild to moderate dementia. Participants will either start VR training right away or after a waiting period, allowing a comparison. The trial measures changes in memory, attention, daily living activities, and quality of life over 15 sessions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Fully immersive virtual reality cognitive training sessions
- What this could lead to
- If effective, this could offer an engaging, non-drug way to support cognitive function and quality of life for people living with dementia.
- What could go wrong
- This is an early feasibility study with a small number of participants, so results may not apply broadly. VR may cause discomfort or be difficult for some people with dementia.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2024
- Expected to finish
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Jul 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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55 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age over 55 years; 2. Diagnosed with mild or moderate dementia (primarily degenerative dementia) by a consulting physician or based on past medical records; 3. A score of at least 11 but no more than 23 on the Mini-Mental State Examination (MMSE); 4. Has at least one family member or a regularly contacted friend (with the person's mobile number and contact at least once a week); 5. Able to walk independently and complete the Timed Up \& Go (TUG) test; 6. Able to follow instructions with or without the assistance of a guardian or therapist; 7. If the assessment indicates moderate dementia, further evaluation will be conducted to determine whether the participant has sufficient capacity to provide informed consent. If their capacity is found to be impaired, the study will be explained to their legal representative Exclusion Criteria: 1. Dementia with Lewy Bodies and other dementia types resulting from specific causes, such as Huntington's Disease, substance addiction, central nervous system infections, nutritional deficiencies, and metabolic disorders. 2. Severe health conditions that may hinder safe participation, such as respiratory distress, severe cardiovascular disease, or brain tumors. 3. A psychiatric diagnosis of psychosis within the past six months. 4. Diagnosis of Korsakoff syndrome. 5. History of substance addiction. 6. Severe hearing impairment or color blindness. 7. History of severe vertigo or epilepsy. 8. Concurrent participation in other studies that may affect cognitive function
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Tucheng Hospital, New Taipei City, commissioned and operated by Chang Gung Medical Foundation.
RECRUITINGNew Taipei City, Taiwan
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