Actively Recruiting
Immersive Virtual Reality and Physical Exercise on Cognitive and Functional Performance in Hospitalized Older Patients
Led by Fundacion Miguel Servet · Updated on 2025-01-13
212
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study will be conducted in a hospital in Spain to investigate how a special intervention using immersive virtual reality technology can benefit hospitalized older adults with difficulties in their daily functionality. The main objective of this study is to evaluate whether a cognitive stimulation intervention through immersive virtual reality, along with specific physical exercises, can improve the cognitive and physical function of hospitalized older patients. It is expected that this innovative intervention will have a positive impact on the quality of life of these patients. Participants eligible for the study must be over 75 years old, have severe functional dependency upon hospital admission, and be willing to participate. Those with severe dementia or other terminal illnesses will be excluded. Participants will be randomly assigned to one of four study groups: a control group without intervention and three intervention groups, including viewing Spanish landscapes through virtual reality, performing specific physical exercises, or a combination of both interventions. At the end of the study, various aspects such as cognitive and physical function, mood, quality of life, muscle strength, and acceptance of virtual reality technology by patients will be evaluated. This study aims to provide new insights into the care of hospitalized older adults and explore innovative ways to improve their well-being during their hospital stay
CONDITIONS
Official Title
Immersive Virtual Reality and Physical Exercise on Cognitive and Functional Performance in Hospitalized Older Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 75 years or older
- Medically stable
- Expected hospital stay of 5 days or more
- Able to communicate and cooperate with the research team
You will not qualify if you...
- Barthel Index score of 60 or higher at admission
- Refusal or inability to give informed consent
- Life expectancy less than three months
- End-stage disease
- Severe major neurocognitive disorder (GDS 7)
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Hospital Universitario de Navarra
Pamplona, Navarre, Spain, 31008
Actively Recruiting
Research Team
N
Nicolas Martinez-Velilla Dr, PhD
CONTACT
F
Fabricio Zambom Dr, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
4
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