Can virtual reality boost brainpower in depressed seniors?
NCT ID NCT07119008
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether virtual reality (VR) can help improve thinking and daily functioning in people aged 70 and older who have depression. Participants will do 12 VR sessions over 6 weeks, doing tasks like sorting groceries or following recipes. The main goal is to see if seniors find VR acceptable and easy to use.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- virtual reality sessions
- What this could lead to
- If this works, it could offer a new, engaging way to help older adults with depression improve their thinking and daily living skills.
- What could go wrong
- This is a small, early-stage study with only 40 participants. It mainly checks if seniors will accept VR, not whether it actually improves depression or thinking. Some people may feel dizzy or uncomfortable using VR.
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 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2028
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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70 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: * Patients aged 70 or over; * Patient with a characterized depressive episode as assessed by the GDS (Score \> 13 at inclusion); * Patient with a minimum MMS score of 23/30 at inclusion; * Patient affiliated to or benefiting from a social security scheme; * Patient having received information on the protocol and having given free, informed and written consent. Exclusion Criteria: * Patients suffering from epilepsy; * Patients suffering from inner ear disorders; * Patients with balance disorders or postural instability; * Patients with swallowing disorders requiring mixed feeding; * Patients suffering from migraines; * Patients with major sensory deficits (visual or auditory); * Patients suffering from eye pathologies or abnormalities, and whose condition strictly contraindicates virtual reality; * Patients suffering from oculo-motor disorders; * Patients with sensory-motor deficits affecting the upper limb(s) that prevent them from performing the tasks required during VR sessions; * Patients suffering from primary neuropathic disorders or secondary to metabolic pathologies; * Patients suffering from acute psychiatric decompensation that makes it impossible for them to cooperate with the sessions (opposition, agitation, acute delusions, hallucinations, panic attacks); * Patients with uncontrolled cardiac pathology (angina, heart failure, rhythm disorders, conduction disorders); * Patients with uncontrolled hypertension (SBP \> 140 mmHg and DBP \> 90 mmHg in patients with traited hypertension); * Patients with implanted medical devices (pacemakers, defibrillators, etc.); * Patients under legal protection (guardianship) or deprived of liberty. * Patients who do not speak or read French fluently, unable to understand the principle of the study questionnaires and unable to cooperate with the tests.
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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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CHU Brest - Hôpital de Bohars
Bohars, 29820, France
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