Actively Recruiting
Non-randomized Clinical Trial on Cognitive Stimulation With Virtual Reality in Patients With Mild Cognitive Impairment
Led by Badalona Serveis Assistencials · Updated on 2025-05-30
60
Participants Needed
1
Research Sites
73 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to find out if adding virtual reality (VR) to a cognitive training program helps improve cognitive performance in older adults with mild cognitive impairment (MCI). In this study, all participants will take part in a 12-week computer-based cognitive rehabilitation program. One group will also use immersive VR for 15-20 minutes at the end of each session. Participants will attend 2 sessions per week, completing at least 20 sessions and up to 22, depending on the clinic's schedule. Researchers will measure changes in attention, memory, and thinking skills using standard cognitive tests. They will also collect feedback on how participants experience the VR exercises.
CONDITIONS
Official Title
Non-randomized Clinical Trial on Cognitive Stimulation With Virtual Reality in Patients With Mild Cognitive Impairment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 60 years or older
- Clinical diagnosis of mild cognitive impairment (MCI)
- Preserved autonomy in basic and instrumental activities of daily living
- MoCA score between 18 and 26
- Ability to use a computer interface with or without assistance
- Capacity to understand and sign informed consent
You will not qualify if you...
- Diagnosis of dementia (MMSE less than 18 or clinical judgment)
- Severe visual or hearing impairment affecting task participation
- History of epilepsy, vertigo, or conditions contraindicating VR use
- Severe psychiatric or neurological illness such as major depression or Parkinson's disease
- Enrollment in other cognitive training programs during the study period
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Centro Socio Sanitario El Carmen
Badalona, Barcelona, Spain, 08917
Actively Recruiting
Research Team
J
José Ferrer Costa, MD
CONTACT
M
Maria Jose Ciudad Mas, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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