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Chronic Aphasia - Improved by Intensive Training and Electrical Brain Stimulation

Chronic Aphasia - Improved by Intensive Training and Electrical Brain

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01221779
Acronym
CATS
Enrollment
40
Registered
2010-10-15
Start date
2011-01-31
Completion date
2014-12-31
Last updated
2013-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anomia (Word-retrieval Impairment), Post-Stroke Chronic Aphasia

Keywords

Intensive language therapy, Anomia, Magnetic Resonance Imaging

Brief summary

The purpose of this study is to determine if non-invasive electrical brain stimulation can enhance the out of intensive language therapy in chronic aphasia

Detailed description

Stroke is the leading cause of death and disability worldwide. Given the increasing average lifespan worldwide, the incidence and prevalence of patients with stroke will dramatically increase in the future. One of the most frequent and devastating conditions after stroke is aphasia, which affects language production and comprehension. High-frequent intensive speech-and-language therapy is currently the treatment of choice in chronic aphasia. However, despite its general effectiveness, treatment effect sizes are only low to moderate. Thus, there is a pressing need to explore novel training-adjuvant therapies to enhance treatment efficacy. Moreover, very little is known about the neurobiology of treatment-induced recovery in chronic aphasia. This is the prerequisite to improve existing and/or develop new treatment paradigms. Thus, in the present project we aim to assess whether the outcome of intensive language training can be enhanced by adjuvant non-invasive brain stimulation. We will be using anodal transcranial direct current stimulation (atDCS) that has previously been shown to enhance (a) language and motor learning in healthy subjects and (b) motor recovery in stroke patients. Specifically, in a longitudinal group comparison design, two matched groups of patients with chronic anomia will receive two weeks of intensive language training with or without atDCS. Treatment effects will be assessed immediately after the two week intervention period and several months after the end of the training. We will also use functional and structural magnetic resonance imaging (MRI) to elucidate language network changes in the two groups.

Interventions

2 weeks of daily computerized naming training, daily, 3 hours

Sponsors

German Federal Ministry of Education and Research
CollaboratorOTHER_GOV
Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* right-handedness * single first time left-hemisphere stroke * fluent- or non-fluent chronic aphasia (more than six months post-stroke) * anomia (PR\>10 and PR\<60 Aachen Aphasia Naming Subtest) * native German Speaker

Exclusion criteria

* more than one stroke * alcoholism, severe psychiatric conditions, other neurological conditions * other non-treated medical problems, severe microangiopathy * pregnancy

Design outcomes

Primary

MeasureTime frame
Boston Naming TestChange of naming score from baseline (day 1 of study) to immediately after 2-week intervention period (post-testing)

Secondary

MeasureTime frameDescription
Boston Naming TestChange of naming score from post-testing (after end of intervention) to 3 months after the intervention (follow-up)The follow-up will be administered to assess the stability of the treatment gains
Naming performance during functional magnetic resonance scanningChange of naming score from baseline (day 1 of study) to immediately after 2-week intervention period (post-testing)assessed during overt picture naming task
Naming performance during functional magnetic resonance imagingChange of naming score from post-testing (after end of intervention) to 3 months after the intervention (follow-up)assessed during overt picture naming task

Countries

Germany

Contacts

Primary ContactMarcus Meinzer, PhD
marcus.meinzer@charite.de+49-(0)30-450-560
Backup ContactAgnes Flöel, MD
agnes.floeel@charite.de+49-(0)30-450-560

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026