tDCS for Post-Stroke Cognitive Impairment

Part of paid clinical trials in Oklahoma City, Oklahoma.

Sponsor
University of Oklahoma
Study ID
NCT06516588
Phase
PHASE2
Status
Recruiting

Conditions

  • Mild Cognitive Impairment
  • Stroke

Eligibility Criteria

Sex
ALL
Age
18 Years - 99 Years
Healthy Volunteers
Not accepted

Interventions

  • Transcranial Dirrect Current Stimulation — DEVICE
    tDCS will deliver direct current through rubber electrodes in saline-soaked sponges. Device sends a low-level current from the positive electrode, the anode, to the negative electrode, the cathode. Direct current will be transferred by a saline-soaked pair of surface sponge electrodes (35cm2) and delivered by a specially developed, battery-driven, constant current stimulator with a maximum output of 10mA. The anode will be placed over the LDLPFC and the cathode over the contralateral supra-orbital area.

Study Details

This study will evaluate the effects of a form of non-invasive brain stimulation on brain functioning and memory in participants with post-stroke cognitive impairment (PSCI).

Key Dates

Start date
Sep 30, 2024
Status verified
Oct 2024
Primary completion
Jun 30, 2026
Completion
Jun 30, 2027

Study Design

Enrollment
80 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Sham Comparator: sham tDCS
    Participants will receive sham (placebo) tDCS for 20 minutes, for 10 sessions
  • Experimental: active tDCS
    Participants will receive active tDCS for 20 minutes, for 10 sessions

Primary Outcome Measure

Montreal Cognitive Assessment (MoCA) [ Time Frame: Changes from baseline after intervention week (two weeks), one and three months ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of OklahomaOklahoma CityOklahoma73117
Cheryl Adams, RN
405-271-8130
Camila Bonin Pinto, PhD (PRINCIPAL_INVESTIGATOR)
Faddi Saleh Velez, MD (SUB_INVESTIGATOR)

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