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NCT05985889 Clinical Trial

Comparison of Innovative Rehabilitation Treatments and Examination of Their Effectiveness in Stroke Patients

Stroke Clinical Trial

Official title:
Comparison of Innovative Rehabilitation Treatments and Examination of Their Effectiveness in Stroke Patients

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT05985889
Other study ID # IKEB/2023/01
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date July 8, 2023
Est. completion date August 30, 2023

Study information
Verified date August 2023
Source Somogy Megyei Kaposi Mór Teaching Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

We perform a comparison of several groups. We would like to determine how robotic and virtual therapy is most effective in the treatment of stroke patients. We place great emphasis on walking speed, quality of life, coordination and changes in walking distance.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 75
Est. completion date August 30, 2023
Est. primary completion date August 30, 2023
Accepts healthy volunteers No
Gender All
Age group 55 Years to 90 Years
Eligibility Inclusion Criteria: post stroke 6MWT : 120> minimum after stroke 3 days be a stroke patient first stroke hemiplegia Exclusion Criteria: multiple strokes, inability to stand and walk, cognitive function disorder does not reach 50 meters with a minimal walking aid Alcohol Sever heart problem sever demeanor alcoholism drug problems Drug

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Robot
You have to walk with a robot mounted on your lower limb. To move, to change direction.
• Fizio
Patients do state-funded physical therapy.
• EXE1
Patients undergo intensive virtual reality therapy once a day.
• EXE2
Patients undergo intensive virtual reality therapy twice a day.
• EXE+ROB
The patients intensively performed 1 virtual reality therapy and 1 robotic therapy every day.

Locations
Country Name City State
Hungary Dr. Tollár József Kaposvár Somogy

Sponsors (1)
Lead Sponsor Collaborator
Somogy Megyei Kaposi Mór Teaching Hospital

Country where clinical trial is conducted

Hungary, 

Outcome
Type Measure Description Time frame Safety issue
Primary mRS score 3 weeks (0-5 score, high score better)
Secondary Barthel index score 3 weeks
Secondary Berg balance score 3 weeks (0-30, high score better)
Secondary 6MWT meter 3 weeks
Secondary 10m gait speed m/s 3 weeks
See also
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Completed NCT03366129 - Blood-Brain Barrier Disruption in People With White Matter Hyperintensities Who Have Had a Stroke
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