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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05027841
Other study ID # E-60116787-020-5302
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date August 13, 2021
Est. completion date August 13, 2022

Study information

Verified date August 2021
Source Istanbul Aydin University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The loss of sensorial feedback causes gait impairment in hemiparesis. The studies show that proprioceptive impairment of knee is related to falling in these patients. The aim of this study is to investigate the effects of proprioception on balance and gait functions in hemiparetic individuals.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 28
Est. completion date August 13, 2022
Est. primary completion date July 13, 2022
Accepts healthy volunteers No
Gender All
Age group 20 Years to 65 Years
Eligibility Inclusion Criteria: - Between the ages of 20-65 and discharged from the hospital, - Diagnosed with hemiparesis at least 4 weeks ago, - First time and unilateral hemiparesis, - Modified Rankin Score = 3, - Hodkinson Mental Test = 6, - Individuals who agree to receive treatment will be included in the study. Exclusion Criteria: - Having vision and hearing problems, - Having other accompanying neurological, psychiatric and/or orthopedic problems other than hemiparesis, - Medically unstable, - Diseases that will affect the lower extremity sense, - Individuals with open wounds, circulation problems, and skin lesions in the area to be treated will be excluded from the study.

Study Design


Intervention

Other:
Proprioseption in hemiparetics
Proprioception on balance and gait functions in hemiparetic individuals

Locations

Country Name City State
Turkey Istanbul Aydin University Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Istanbul Aydin University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sensorial Assessment-1 Semmes-Weinstein Monoflament 2 minutes
Primary Sensorial Assessment-2 Position test for lower extremity 2 minutes
Primary Sensorial Assessment-3 Kinestesia (Electrogoniometer) 2 minutes
Primary Balance assessment Static balance via SportKAT-550 30 second
Primary Gait parameters BTS G-Walk Spatiotemporal gait parameters 1 minute
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