Transcranial Direct Current Stimulation (tDCS) in Chronic Post-Stroke Apathy
Stopped early · Not applicable
Conditions studied: Apathy, Stroke
In brief
The purpose of this study is to test the efficacy and safety of tDCS (Transcranial Direct Current Stimulation) on apathy in stroke patients.
Key facts
- Study ID
- NCT02915484
- Run by
- Stony Brook University
- People needed
- 12
- Starts
- 2016-06-01
- Expected to finish
- 2017-06-01
- Last updated by the study team
- 2017-10-03
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Clinical diagnosis of stroke and radiographically proven ischemic or hemorrhagic stroke (MRI required for ischemic stroke, CT sufficient for hemorrhagic stroke)
- Stroke occurred at least one month prior to first stimulation session
- Ability to provide informed consent
- Availability of a family member / caregiver who knew the subject before the stroke and interacts with the subject on at least a weekly basis
- Score of 6 or higher in initial apathy testing using Apathy Inventory - Clinician score
- Speak English (required for quantifying apathy and performing the cognitive tests)
You may not qualify if…
- Other potential cause of apathy including some neurodegenerative diseases, some psychiatric diseases, and anti-dopamine medication
- Prior brain injury (e.g., Traumatic Brain Injury (TBI), stroke) without full motor and cognitive recovery based on patient, family or clinician report
- Active medical illness (e.g., infection, delirium, etc.) that might affect arousal and cognitive function
- Hypoarousal (inability to maintain eye opening without stimulation) from any cause (e.g., stroke, sleep deprivation)
- Any history of epilepsy
- Recent drug or alcohol abuse - within the past year
- Pregnant or breastfeeding
- Moderate to severe aphasia preventing subject from communicating fully
- Any pacemakers, intracranial electrodes, implanted defibrillators, or any other electrical implants
Where it is running
- Stony Brook University — Stony Brook, New York, United States
Full record on ClinicalTrials.gov
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