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Recruiting Not applicable NCT05907265

Immersive Virtual Reality Techniques on the Effects on Cognition in People With Cancer

No applicable phase (e.g. observational)
Conditions: Cancer Cognitive Impairment

Sponsor: Consorci Sanitari de Terrassa

trial.available_in: БГ
Overview
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.
Who can participate
Inclusion Criteria: A. Over 18 years of age and under 65 years of age B. Diagnosis of cancer C. At least 4 weeks since the last chemotherapy treatment session D. Presence of cognitive complaints after chemotherapy treatment E. Level of primary education to be able to perform the cognitive tests. F. Consent to participate in the study Exclusion Criteria: A. Established diagnosis prior to cancer diagnosis of psychiatric, neurological, neurodevelopmental or systemic disorder causing cognitive deficits. B. Motor or sensory impairments that preclude completion of the program. C. Undergoing chemotherapy treatment
Interventions
Behavioral: ONCOBrain_ImmersiveVR
BEHAVIORAL
Behavioral: Control_Condition
BEHAVIORAL
Locations 1
Spain (1)
Consorci Sanitari de Terrassa
Terrassa
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
65 Years
Healthy volunteers
No
Start date
01.05.2023
Completion date
30.06.2027
Registry ID
NCT05907265
Source
clinicaltrials.gov
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