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Transcranial Direct Current Stimulation to Enhance Training Effectiveness in Chronic Post-Stroke Aphasia

StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record status
This record was last updated May 16, 2025 (before its estimated February 4, 2026 completion). Its status may not reflect the trial's current state.

Record History

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  1. Notable Primary completion date: Feb 4, 2025 to Feb 4, 2026
    • Trial status: Recruiting to Active, Not Recruiting
    • Study sites: 18 to 19
    • Study completion date: Aug 4, 2025 to Aug 4, 2026
    v9
  2. Notable Primary completion date: Feb 4, 2024 to Feb 4, 2025
    • Study completion date: Aug 4, 2024 to Aug 4, 2025
    v8
  3. Minor Site contacts updated at 1 of 18 sitesv7
  4. Minor Eligibility criteria revisedv6
  5. Notable Primary completion date: Oct 1, 2022 to Feb 4, 2024
    • Study completion date: Mar 31, 2023 to Aug 4, 2024
    v5
Show 3 earlier versionsHide 3 earlier versions
  1. Minor Re-verified, no change to tracked fieldsv4
  2. Minor Eligibility criteria expanded, about 20 wordsv3
  3. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Sep 1, 2019 to Dec 6, 2019
    • Study sites: 1 to 18
    • Secondary endpoints: details revised at 1 of 11 entries
    v2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The aim of the study is to investigate whether intensive speech-language therapy (SLT) combined with anodal transcranial direct current stimulation (tDCS) leads to better communication performance than SLT combined with placebo stimulation (using sham-tDCS).
Trial Details
NCT Number NCT03930121
Lead Sponsor University Medicine Greifswald
Conditions
(from sponsor)
Aphasia, Post-stroke
Related terms Aphasia
Enrollment 130 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov