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Clinical Trials/RBR-539w5nw
RBR-539w5nw
Active, not recruiting
未知

Balance Training in hemiparetic patients through Virtual Rehabilitation

Centro Universitário Central Paulista0 sitesJuly 8, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
Ischemic stroke
Sponsor
Centro Universitário Central Paulista
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

The study aimed to evaluate the effectiveness of balance training in hemiparetic individuals using VR and compare it to conventional training. This randomized controlled clinical trial included 16 patients; of both genders, aged between 30 and 60 years, diagnosed with ischemic CVA (CVAi) and Hemiparesis sequelae; divided into two groups, where the first (GTE) performed conventional training and the second (GRV) conventional associated with VR with Xbox/Kinect. Assessed using the Berg Balance Scale (BSE) and the 10-meter Gait Speed Test (TVM10m). The results showed that both conventional balance training and that associated with VR were beneficial, showing a significant difference (p<0.05). However, in the intergroup comparison, training with VR was more effective for TVM10m. Concluding that VR had significant additional effects on the balance of chronic hemiparetic patients and, although it does not replace traditional rehabilitation, it can be a differential resource, when used as an adjunct to physical therapy treatment.

Registry
who.int
Start Date
July 8, 2022
End Date
December 15, 2012
Last Updated
2 years ago
Study Type
Intervention

Investigators

Sponsor
Centro Universitário Central Paulista

Eligibility Criteria

Inclusion Criteria

  • Volunteers who suffered ischemic stroke; of both genders; age between 30 and 60 years; sequelae of hemiparesis for at least 6 months

Exclusion Criteria

  • Volunteers who had other illnesses not related to the stroke; those who were in the acute or subacute phase of the disease; those who suffered a hemorrhagic stroke; hemiplegics; amputees; wheelchair users or orthotics; visually and/or hearing impaired; those who could not understand or respond to data collection instruments

Outcomes

Primary Outcomes

Not specified

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