| Registry | NCT04533308 |
|---|---|
| Status | Completed |
| Phase | Not applicable |
| Study type | Interventional; randomized, parallel, masking: none, other |
| Enrollment | 40 (Actual) |
| Sponsor | State Budgetary Healthcare Institution, National Medical Surgical Center N.A. N.I. Pirogov, Ministry of Health of Russia (Other) |
| Conditions | Aphasia, Virtual Reality, Emotional Disturbances |
| Interventions | Relaxation in virtual reality (Behavioral) |
| Dates | start 2020-08-20, primary completion 2021-09-01, completion 2022-08-01, first posted 2020-08-31, last updated 2022-11-01 |
| Locations | 1 site in Russia |
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The aim of the study is to determine virtual reality (VR) impact during standard program of rehabilitation on emotional state of patients with aphasia.
Aim 1: To test the safety of virtual reality in a vulnerable population of patients with aphasia during rehabilitation. Participants will be alternately assigned to receiving a relaxation session in VR every working day during a standard course of rehabilitation.
Aim 2: To test the preliminary efficacy of combining VR with the course of rehabilitation to promote emotional improvements in patients with aphasia.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| VR intervention | Experimental | Behavioral: Relaxation in virtual reality | Participants will have a session in VR for 20-30 minutes each working day. They can choose natural 360-degrees scenes from different locations in the world with or without interactions with animals. The equipment will include HTC Vive (HTC Corporation). |
| Control | No intervention | Patients in the control group will not receive any psychological interventions. |
Sex: All, ages: 18 Years to 75 Years
Inclusion Criteria: * Mild or moderate aphasia of any type * Russian is primary language * At least 2 weeks post cardio-vascular accident (ischemic or hemorrhagic stroke) or head injury of any location * Have a history of only one stroke * Medically stable Exclusion Criteria: * Associated severe cognitive deficits and psychiatric disorders which prevent patients understanding of the informed consent * Epilepsy * Medical history of severe visual or hearing impairment * Comorbid neurological diagnosis (e.g. epilepsy, multiple sclerosis, Parkinson disease, dementia) * Unable to perform the required exercises due to severe motor, sensory or cognitive deficit (memory, attention, executive functioning, apraxia, regulatory and planning activities etc.) and medical problems (for example, anyone meeting New York Heart Association Class IV criteria, hospitalization for myocardial infarction or heart surgery within 120 days, severe cardiomyopathy or documented serious and unstable cardiac arrhythmias) * Drug or alcohol addiction within the last 6 months. * Significant current psychiatric illness defined as affective disorder unresponsive to medication or bipolar affective disorder, psychosis, schizophrenia or suicidality * Current participation in another interventional trial
| Facility | City | Country | Status |
|---|---|---|---|
| Pirogov National Medical and Surgical Center | Moscow | Russia |