Neuro-rehabilitation Training Effects on Motion and Quality of Life After Acute Stroke and Post Stroke

Stroke Clinical Trial

Official title:

Neuro-rehabilitation Training Effects on Motion and Quality of Life After Acute Stroke and Post Stroke

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03736200
• Other study ID #: IKEB008/2018
• Status: Completed
• Phase: N/A
• Start date: September 1, 2018
• Est. completion date: November 1, 2019

Study information

• Verified date: September 2018
• Source: Somogy Megyei Kaposi Mór Teaching Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 2
• Est. completion date: November 1, 2019
• Est. primary completion date: November 1, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 55 Years to 80 Years

Eligibility

Inclusion Criteria:

• post stroke

• 6MWT : 120>

• minimum after stroke 2 weeks

Exclusion Criteria:

• Sever heart problem

• sever demeanor

• alcoholism

• drug problems

Related Conditions & MeSH terms

• Stroke

Intervention

Other:
• Exergaming group
Neurorehabilitation - 4-week-long intervention, targeted postural instability and mobility using at-limit intensity sensori and visuomotor agility training. (1/day)
• Physiotherapy
Physiotherapy 4-week-long.
• Exergaming group 2/day
Neurorehabilitation - 4-week-long intervention, targeted postural instability and mobility using at-limit intensity sensori and visuomotor agility training. (2/day)

Locations

Country	Name	City	State
Hungary	József Tollá	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	Quality of life measured by Barthel index	questionnaire	4 weeks
Primary	gait / functional test	6 minute walk test (m)	4 weeks
Primary	balance test	Berg balance test	4 weeks
Primary	postrural control test	posturography (mm)	4 weeks
Primary	Quality of life measured by EQ5-D scale	questionnaire	4 weeks

External Links

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