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Набира участници Не е приложимо NCT05907265

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

Не е приложима фаза (напр. обсервационно)
Заболявания: Cancer Cognitive Impairment

Спонсор: Consorci Sanitari de Terrassa

Налично на: БГ
Обобщение
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.
Кой може да участва
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
Интервенции
Behavioral: ONCOBrain_ImmersiveVR
BEHAVIORAL
Behavioral: Control_Condition
BEHAVIORAL
Места на провеждане 1
Испания (1)
Consorci Sanitari de Terrassa
Terrassa
Технически детайли
Статус
Набира участници
Фаза
Не е приложимо
Вид изследване
INTERVENTIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Максимална възраст
65 Years
Здрави доброволци
Не
Начална дата
01.05.2023
Крайна дата
30.06.2027
Регистрационен номер
NCT05907265
Източник
clinicaltrials.gov
Запитване за медицински туризъм

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