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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05483556
Other study ID # HSEARS20220211001
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2021
Est. completion date October 31, 2024

Study information

Verified date January 2024
Source The Hong Kong Polytechnic University
Contact Min Ney WONG, PhD
Phone (852) 27667268
Email min.wong@polyu.edu.hk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The efficacy of conventional speech therapy alone for aphasia recovery is inconclusive. The prospective study will monitor the effects of combined language therapy and tDCS through structural and functional MRI.


Description:

The efficacy of conventional speech therapy alone for aphasia recovery is inconclusive. The prospective study will monitor the effects of combined language therapy and tDCS through structural and functional MRI. This randomized, placebo-controlled, double-blinded pilot study will recruit ten chronic stroke patients with Broca's Aphasia randomly assigned either to sham or an anodal tDCS groups. Following speech and language assessment, all the participants will receive 20 minutes of individualized language therapy daily for ten days in two consecutive weeks. Simultaneously, the treatment group will receive 20 minutes of 2mA anodal HD-tDCS over the left IFG, while the sham group will receive the 30s of 2mA anodal HD-tDCS. Structural, resting state and task activated functional MRI will be performed. Data acquisition will be performed before, immediately after and two months after the treatment. Repeated measure ANOVA for changes in picture-naming accuracy and response time will be performed as a within-subject factor between sham and anodal tDCS. Pearson's correlation coefficient of left IFG and its homolog in the right hemisphere through Independent component analysis (ICA) of low-frequency fluctuations in resting-state and task activated state will be compared for functional connectivity analysis for IFG and other major languages hubs for oral language production between groups.


Recruitment information / eligibility

Status Recruiting
Enrollment 10
Est. completion date October 31, 2024
Est. primary completion date October 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: 1. History of a single unilateral left-hemispheric stroke, 2. Right handedness 3. Demonstrated features of Broca's Aphasia 4. Cantonese speaker 5. Comprehension sufficient to carry out tasks 6. No history of other neurological diseases Exclusion Criteria: 1. Aphasia due to reasons other than Stroke, Traumatic brain injury 2. Bilateral or multiple brain lesions 3. Wernicke's aphasia and other speech disorders, degenerative, psychiatric or metabolic disorders 4. Deaf, blind, pregnant/ or preparing for pregnancy, cognitive issues, tattoos 5. Have cochlear implants, pacemaker, surgical nails for bone fracture, artificial joints, dental braces, dentures 6. Taking anti-depressant medications

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Real tDCS
An anodal high-definition tDCS of 2 mA lasting for 20 minutes will be delivered to the left inferior frontal gyrus during speech therapy.
Sham tDCS
An anodal high-definition tDCS of 2 mA lasting for 30 seconds will be delivered to the left inferior frontal gyrus during speech therapy.

Locations

Country Name City State
Hong Kong The Hong Kong Polytechnic University Kowloon

Sponsors (1)

Lead Sponsor Collaborator
The Hong Kong Polytechnic University

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Primary Picture naming Picture-naming accuracy and response time for each stimuli will be determined perceptual and calculated using praat software Change before, immediately after and two months after the treatment
Secondary Imaging analysis Mapping changes in functional connections of language networks, inter-hemispheric and intra-hemispheric regions of the brain. Change before, immediately after and two months after the treatment.
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