Efficacy of Recreational-therapeutic Use of Video Games on the Emotional State of Stroke Patients
Stroke, Acute, Virtual Reality
About this trial
This is an interventional supportive care trial for Stroke, Acute
Eligibility Criteria
Inclusion Criteria:
- To be of legal age
- Fluent in oral and written Spanish.
- Patients with cognitive functions of expression and comprehension.
Exclusion Criteria:
- Patients who are not undergoing neurorehabilitation treatment.
- Patients who have not yet started rehabilitation treatment.
Sites / Locations
- Fundación Instituto San Jose
- CEADAC
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Control
Intervention Group
The variables to be filled in upon admission are: age, sex, reason for admission and main caregiver. The variables that will be collected on admission and discharge are: Mississippi Aphasia Screening test, Canadian scale, Duke-UNK-11 subjective support scale, UCLA loneliness scale, oropharyngeal dysphagia screening test, Pfreiffer scale, State assessment mood, Hamilton Rating for Depression and Hospital Anxiety Depression Scale and HLS-EU Q16., Will be performed on all patients who are part of the trial. Those patients where conventional rehabilitative treatment is performed will be: Physiotherapy sessions Speech therapy sessions Neuropsychology sessions Occupational therapy sessions
The variables are to be filled in upon admission are: age, sex, reason for admission and main caregiver. The variables that will be collected on admission and discharge are: MAST, Canadian scale, Duke-UNK-11 subjective support scale, UCLA loneliness scale, oropharyngeal dysphagia screening test, Pfeiffer scale, State assessment mood, Hamilton Rating for Depression and Hospital Anxiety Depression Scale and HLS-EU Q16.The beginning of the intervention will be once you have completed 15 calendar days from your admission.The intervention will be carried out once a week with a duration of 20 min with one of the games chosen by the patient together with the physiotherapist.The completion of the intervention will be until the patient is discharged from hospital, with a minimum of four sessions carried out in order to participate in the study.A registration table will be executed where the number of sessions of each patient and the type of session are quantified like a control group.