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NCT05612659Completed

Developing an EEG Probe for Studying and Modulating Cognitive Control

Developing an EEG Probe for Studying Effects of Non-invasive Cortical and Spinal Cord Electrical Stimulation on Cognitive Control in Post Stroke Depression

Source: ClinicalTrials.gov · Last updated 27 Jun 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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)

Status (registry)
Completed
Study type
Interventional
Enrollment
30 (actual)
First submitted
31 Oct 2022
Start date
28 Sept 2022
Primary completion date
31 Mar 2024
Lead sponsor
University of Cincinnati
Diseases
Stroke
NCT number
NCT05612659

What you commit to

  • Study type: Interventional
  • Participants enrolled: 30
  • From 28 Sept 2022 to the primary completion date, 31 Mar 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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);

Other illness

  • Current or lifetime bipolar disorder or schizophrenia diagnosis;
  • current (past month): PTSD, psychotic or substance use disorder (nicotine and caffeine allowed);
  • current chronic severe pain conditions;

Other

  • significant risk of suicide according to CSSRS or clinical judgment, or suicidal behavior in the past year:
  • 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.

Who the study is looking for

  • 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 stroke

Age in the registry: 18 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Cincinnati
Coordinator of this site? Confirm its status
CincinnatiUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.