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Virtual Therapy in Rehabilitation Spastic Hemiparesis

U

Universidade do Vale do Paraíba

Status

Unknown

Conditions

Stroke

Treatments

Other: conventional physiotherapy
Other: virtual therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT02061371
20749113.5.0000.5503

Details and patient eligibility

About

Evaluate the effectiveness of virtual therapy and conventional physiotherapy in spastic muscles of patients with sequelae of stroke.

Full description

Considered the second most frequent cause of death worldwide , the stroke is also responsible for the largest number of functional disability in individuals. The socio - economic hardship that many patients face to perform a program of intensive rehabilitation sensorimotor, has led to functional limitations in many cases , promote irreversible consequences. Spasticity in the upper and lower limb after stroke results in loss of function and mobility being the key therapeutic approaches in order to restore its function. Currently, the Virtual therapy has been used in physical therapy, demonstrating safety, feasibility and potential to facilitate the effective rehabilitation treatment, promoting motor recovery. The objective of this study is to analyze and compare the effectiveness of virtual therapy and conventional physiotherapy in paretic upper and lower limbs of patients with sensory motor deficit after stroke. Virtual therapy will be based on a custom application using virtual reality projection, and conventional treatment will be based on cinesiotherapy for members upper and lower paretic. The evaluation will be performed by biomedical instrumentation using dynamometry, electromyography and analysis from functional movement. Statistical differences are based on t test with significance level of p 0 , 05 . As a result expected - scientifically proven the effectiveness of this new form of treatment aimed at improving quality of life and functional independence of patients with neurological sequel.

Enrollment

40 estimated patients

Sex

All

Ages

40 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Medical referral for physiotherapy;
  • Maximum grade 2 spasticity in the upper and lower limbs according to the Modified Ashworth Scale;
  • Total passive range of elbow joint and knee to the movement of flexion and extension;
  • Independent ambulation, with or without support;
  • Cognitive preserved, being able to respond to the command of the examiner;
  • Least 6 months of injury;

Exclusion criteria

  • Active infection, and rash at the site of application of NMES;
  • Visual and hearing impairment;
  • Joint stiffness and musculoskeletal injuries of the elbow and knee,
  • Inability to interpret the therapeutic resources to be displayed;
  • Presenting lesions in areas of Wernick and drill;
  • Uncontrolled hypertension.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

40 participants in 2 patient groups

virtual therapy
Experimental group
Description:
Group 1 (G1) included 20 patients who will carry out the virtual therapy.
Treatment:
Other: virtual therapy
conventional physiotherapy
Experimental group
Description:
Group 2 (G2) included 20 patients who hold conventional physiotherapy.
Treatment:
Other: conventional physiotherapy

Trial contacts and locations

1

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Central trial contact

Ana Carolina Borges, masters students; Mário Oliveira Lima, professor

Data sourced from clinicaltrials.gov

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