Clinical Trial

A rTMS and Virtual Reality Based Cognitive Rehabilitation Program for MCI

Study acronym: rTMS+iVCT
Recruiting
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Record status
This record was last updated February 20, 2025 (before its estimated March 31, 2026 completion). Its status may not reflect the trial's current state.
Summary
This clinical trial is being conducted to see if brain stimulation and brain training together improves cognitive functioning and mood in older adults diagnosed with Mild Cognitive Impairment (MCI). Brain stimulation will be done using repetitive Transcranial Magnetic Stimulation (rTMS). Brain training will be done using immersive virtual reality cognitive training (iVCT) program. The goals of this clinical trail are as follows: * Examine if rTMS+iVCT intervention can improve and sustain objective cognitive functioning in individuals with MCI more than control or rTMS only groups * Examine if rTMS+iVCT intervention improves participants mental health symptoms, functional abilities, and quality of life more than control or rTMS only groups * Examine the impact of rTMS+iVCT intervention on caregiver burden. Eligible participants will be assigned to a standard treatment (no intervention control) group, rTMS only group of rTMS+iVCT group. All participants will undergo baseline assessment to evaluate their cognitive, emotional, and functional abilities. Those in the rTMS only group will receive rTMS treatments for five days per week for two weeks (total of ten sessions). Those in the rTMS+iVCT group will receive rTMS treatment followed by iVCT training for five days a week for two weeks (total of ten sessions). All participants will then repeat testing 2 weeks and three months after baseline testing to assess for possible treatment related changes and lasting effects.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2023-09-05.
Status change: Not Yet Recruiting → Recruiting 2025-02-19
Trial Details
NCT Number NCT06024473
Lead Sponsor Central Arkansas Veterans Healthcare System
Conditions Mild Cognitive Impairment, Caregiver Burden, Mental Health Issue, ADL, Quality of Life
Enrollment 50 participants
Start Date 2024-03-31
Primary Completion 2026-03-31 (estimated)
Study Completion 2026-09 (estimated)
Updated on ClinicalTrials.gov 2025-02-20