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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06361901
Other study ID # 2023GR0452
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 17, 2023
Est. completion date December 2024

Study information

Verified date April 2024
Source Korea University Guro Hospital
Contact Seung Nam Yang, MD, PhD
Phone 82-2-2626-1500
Email snamyang@korea.ac.kr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Our study will provide precise and intensive speech rehabilitation treatment program to patients with speech disorders after stroke, and compare clinical evaluations with the conventional speech therapy patient group. Clinical evaluation tools will be performed before and after the treatment for all patients - K-Western Aphasia Battery for aphasia assessment tools - Cerebral blood flow changes with near-infrared spectroscopy


Description:

During the initial evaluation of this study, the patient's gender, age, and onset of stroke lesion occurrence are collected and a cognitive evaluation is performed. In addition, the K-Western Aphasia Battery for aphasia assessment tools(K-WAB) and Cerebral blood flow changes with near-infrared spectroscopy will be performed. All participants will be assigned to a test group or control group. In addition to the existing speech rehabilitation treatment, the test group will receive a speech rehabilitation program, and the control group will receive the same treatment as the existing speech rehabilitation treatment. After treatment is completed, the K-WAB test and near-infrared spectroscopy will be performed again.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria: - Adults over 19 years old - Those with speech disorders that occurred after a stroke was diagnosed - Those who can follow the clinical study procedures - Those who voluntarily signed the consent form Exclusion Criteria: - Patients who have difficulty to consent to research and participate in speech rehabilitation programs due to cognitive decline

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Zenicog;language rehabilitation program
This program is an AI-based computerized cognitive and language training program.
Procedure:
Conventional language rehabilitation
Conventional language rahabilitation therapy will apply for all participants with speech impairement

Locations

Country Name City State
Korea, Republic of Department of Rehabilitation Medicine, Korea University Guro Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Korea University Guro Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Aphasic quatient Aphasic quatient using K-Western Aphasia Battery for aphasia assessment tools Evaluate two times ; Before speech therapy treatment program (baseline) and within 7days after the treatment period.
Secondary Change of cerebral blood flow Change of cerebral blood flow with near-infrared spectroscopy Evaluate two times ; Before speech therapy treatment program (baseline) and within 7days after the treatment period.
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