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Follow-up Study of the Effectiveness of Virtual Reality Therapy in Patients With Stroke

S

Somogy Megyei Kaposi Mór Teaching Hospital

Status

Completed

Conditions

Stroke

Treatments

Other: Neurorehabilitation
Other: Physiotherapy

Study type

Interventional

Funder types

Other

Identifiers

NCT04587349
IKEB2020/06

Details and patient eligibility

About

High intensity motion improves motor functions and quality of life in a neurologist. The investigators want to improve the clinical condition and quality of life of post-STROKE participants with a special sensory motor and visual motor agility therapy. High intensity motion improves engine function and quality of life in a neurologist. With special sensory motor and visual motility, investigaters want to improve the clinical condition and quality of life of STROKE participants. The investigaters randomly select participants who only perform the rehabilitation treatment have performed. The other group that will receive the study's control group will receive the traditional rehabilitation physiotherapy treatment. The investigaters assess the condition and quality of life of the patients. (EQ5-D, Barthel index, MRS test) The ivestigaters examine the functional movement and equilibrium variables of patients. (6MWT, Berg balance test, postgraduation) After that, participants are undergoing a 4-week intensive rehabilitation treatment. All participants are in post stroke. Primary Hypothesis will be changes in life-quality tests (EQ5-D, Barthel index, MRS test). Functional tests show progress 6MWT, Berg balance test and postural control testing with posturography. The results are compared and evaluated among the groups. The expected hypothesis is that visual and acoustic stimulation produces a better physical state at higher intensity. Patients were followed for 2 years and participated in a follow-up study every six months.

Enrollment

2 patients

Sex

All

Ages

55 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

• post stroke

Exclusion criteria

  • Sever heart problem
  • sever demeanor
  • alcoholism
  • drug problems

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

2 participants in 4 patient groups

Exercise+FU 2/week
Active Comparator group
Description:
Post stroke group that received 2 years of intensive therapy. (2/week)
Treatment:
Other: Neurorehabilitation
Other: Neurorehabilitation
Exercise+FU 3/week
Active Comparator group
Description:
Post stroke group that received 2 years of intensive therapy. (3/week)
Treatment:
Other: Neurorehabilitation
Other: Neurorehabilitation
physiotherapy
Active Comparator group
Description:
Post stroke group that received 2 years of traditional physiotherapy. (3/week)
Treatment:
Other: Physiotherapy
Exercise+FU - controll
No Intervention group
Description:
He did not receive treatment after 4 weeks of intensive care. it functions only as a control group.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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