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Non-invasive Brain Stimulation
ACTIVE for Repetitive Transcranial Magnetic Stimulation
N/A
Waitlist Available
Research Sponsored by Palo Alto Veterans Institute for Research
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
Study Summary
This study is evaluating whether repetitive transcranial magnetic stimulation may help improve memory for individuals with traumatic brain injury.
Eligible Conditions
- Repetitive Transcranial Magnetic Stimulation
- Traumatic Brain Injury
- Memory Loss
- Aging
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
CANTAB Paired Associates Learning (PAL)
Secondary outcome measures
Functional Connectivity Changes in the Brain
Other outcome measures
Quality of Life measure: Short Form of Veterans Rand 36 Item Health Survey (SF/VR-36)
Sustained Improvement in Measure (CANTAB Paired Associates Learning (PAL)) at 6 months post-treatment
Trial Design
2Treatment groups
Active Control
Group I: ShamActive Control1 Intervention
Patients with mild and moderate TBI will be assigned randomly to this arm and will not receive treatment
Group II: ACTIVEActive Control1 Intervention
Patients with mild and moderate TBI will be assigned randomly to this arm and will receive treatment
Find a Location
Who is running the clinical trial?
Stanford UniversityOTHER
2,382 Previous Clinical Trials
17,333,657 Total Patients Enrolled
Palo Alto Veterans Institute for ResearchLead Sponsor
52 Previous Clinical Trials
7,872 Total Patients Enrolled
The Defense and Veterans Brain Injury CenterFED
19 Previous Clinical Trials
2,688 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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