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NCT05612659
Developing an EEG Probe for Studying and Modulating Cognitive Control
Conditions: Post-stroke Depression
Sex: All
Ages: 18 Years – 80 Years
Healthy volunteers: 1
Phase: NA
Enrollment: 15
Sponsor: University of Cincinnati
Location: United States
Summary
This study aims to investigate effects of transcranial current stimulation (tES) and transcutaneous direct current stimulation (tsDCS) associated changes on fronto-parietal EEG and cognitive performance in patients with post stroke depression (PSD)
Eligibility Criteria
Inclusion Criteria:Subjects will include both male and female of age over 18 years and a BMI of 18-35 Kg/mts2 who have experienced stroke.Moderately depressed, MADRS:18-28, PHQ9: 10-20 and/or experiencing cognitive impairments after strokeExclusion Criteria:Current or lifetime bipolar disorder or schizophrenia diagnosis;current (past month): PTSD, psychotic or substance use disorder (nicotine and caffeine allowed);significant risk of suicide according to CSSRS or clinical judgment, or suicidal behavior in the past year:current chronic severe pain conditions;current chronic use of: opioids analgesics, medications that affect blood pressure or drugs with significant autonomic effects (stimulants and antipsychotics allowed if dose stable for 1 month);skin lesions on electrode placement region;implanted electrical medical devices;Pregnancy;suspected IQ<80, and 10) any other clinically relevant reason as judged by the clinician.
Source: ClinicalTrials.gov (NCT05612659). StuddyBuddy aggregates publicly available trial information.