About this trial
A randomized comparative study will be conducted to evaluate the rehabilitation process using a VR-based application versus conventional therapy in 40 patients (sample size determined using a sample size calculator). After meeting the eligibility criteria, participants will be randomly assigned to two groups: the experimental group (20 patients with gait pattern asymmetry), performing a gait training program using a VR rehabilitation application, and the control group (20 patients with gait pattern asymmetry), performing only a conventional gait training program.
Participants in both groups will take part in a 2-week rehabilitation program (Monday to Friday), with daily training sessions lasting up to 2 hours. Patient assessment will be conducted twice: an initial evaluation before the start of the intervention (Assessment I) and a follow-up evaluation after completion of the 2-week program (Assessment II), at the same time of day, under the same conditions, and using the same measurement tools.
Eligibility criteria
Qualifiers
Diagnosed and clinically confirmed gait pattern asymmetry in the course of neurological diseases
Informed consent to participate in the study and willingness to comply with rehabilitation recommendations
Disqualifiers
Active rheumatic diseases, cancer, advanced diabetes, cardiovascular diseases, and other conditions that may affect the safety and effectiveness of rehabilitation
Contraindications to VR therapy (epilepsy, motion sickness, dizziness, nausea)
Lower limb injuries or surgeries within the last 6 months
Severe mental disorders preventing understanding of instructions
Trial design
Treatments tested in this trial
- Virtual Reality (VR) and Standard Rehabilitation
- Standard Rehabilitation