Actively Recruiting
Immersive Virtual Reality Techniques on the Effects on Cognition in People With Cancer
Led by Consorci Sanitari de Terrassa · Updated on 2026-04-17
60
Participants Needed
1
Research Sites
217 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
OncoBRAIN aims to assess the effect of an innovative immersive virtual reality-based (IVR) intervention that includes cognitive, physical activity and mindfulness exercises in people diagnosed with cancer and Chemotherapy-Related Cognitive Deficits (CRCD). The main objective of OncoBRAIN is to determine the benefits of RVI intervention on the cognitive, and emotional state and quality of life of people with cancer and CRQD. We hypothesize that in OncoBRAIN we will find improvements in people with cancer and CRCD who have received IVR stimulation compared to the control group with cancer and CRCD who have not received IVR stimulation. People in the experimental group will perform better than patients in the control group in cognition (episodic memory, executive function, attention, and information processing speed), show better emotional well-being and perceive a better quality of life at the end of the intervention.
CONDITIONS
Official Title
Immersive Virtual Reality Techniques on the Effects on Cognition in People With Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Over 18 years of age and under 65 years of age
- Diagnosis of cancer
- At least 4 weeks since the last chemotherapy treatment session
- Presence of cognitive complaints after chemotherapy treatment
- Level of primary education sufficient to perform cognitive tests
- Consent to participate in the study
You will not qualify if you...
- Established diagnosis before cancer of psychiatric, neurological, neurodevelopmental, or systemic disorder causing cognitive deficits
- Motor or sensory impairments that prevent completion of the program
- Currently undergoing chemotherapy treatment
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Consorci Sanitari de Terrassa
Terrassa, Spain, 08227
Actively Recruiting
Research Team
M
Maite Garolera
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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