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NCT07433972Recruiting

Changes in Hemodynamic Response Following Transcranial Electrical Stimulation in Sroke Individuals

Source: ClinicalTrials.gov · Last updated 8 Oct 2026

Brief summary (registry, in English)

The present study will use transcranial electrical stimulation (tES) which are transcranial direct current stimulation (tDCS) and transcranial alternating current stimulation (tACS) combined with conventional physical therapy and cognitive-motor dualt ask gait training in sub-acute (at least 2 weeks after stroke onset) to chronic stroke (within 5 years post-stroke) to investigate changes in brain hemodynamics (oxy-hemoglobin and deoxy-hemoglobin concentration) as measured by functional near infrared spectroscopy (fNIRS). The findings may provides insights changes in combining tES with rehabilitation on improvements in brain hemodynamics in sub-acute to chronic stroke.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
19 Feb 2026
Start date
1 Mar 2026
Primary completion date
30 Mar 2027
Lead sponsor
Mahidol University
Diseases
Stroke
NCT number
NCT07433972

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 1 Mar 2026 to the primary completion date, 30 Mar 2027
  • 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

  • Receiving other non-invasive brain stimulation or additional intervention such as TMS, PMS or acupuncture

Other illness

  • Presence of any psychological or neurological antecedent, unstable medical conditions or condition that may increase risk of stimulation such as epilepsy, seizure, and history of brain injury
  • Having unstable cardiovascular disease or respiratory disease, and uncontrolled chronic disease such as diabetes mellitus (DM), hypertension (HT) and chronic kidney disease (CKD)
  • Presence of metal implantation, intracranial shunt, cochlear implantation, or cardiac pacemakers.

Other

  • Presence of an opened wound, infectious wound around scalp or craniectomy with unreplaced bone flap
  • Moderate pain (numeric pain rating score \> 4/10) in any joint of the upper or lower limb, whether paretic or non-paretic
  • Presence of color blindness
  • Presence of any substance use including cannabis and kratom

Who the study is looking for

  • Unilateral stroke individuals aged 18-80 years.
  • A first-ever stroke.
  • Stroke onset from at least 2 weeks-5 years.
  • Able to walk independently with or without gait aids (modified Rankin scale (mRS) 1-3)
  • Montreal cognitive Assessment-Thai version (MoCA-T) greater than or equal to 20 scores.
  • Ability to read, communicate, follow and understand instructions.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept 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
Faculty of Physical Therapy, Mahidol University
Coordinator of this site? Confirm its status
SalayaThailandRecruiting

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