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Study identifier: NCT05699226 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Amplitude Titration to Improve ECT Clinical Outcomes

Condition: Depression · ECT · Cognitive Change  ·  Sponsor: University of New Mexico

PhaseNA
Planned participants50
Who can joinAll sexes, 50 Years to no upper limit
Healthy volunteersNo

About this study

A randomized controlled trial will compare hippocampal neuroplasticity, antidepressant, and cognitive outcomes between individualized amplitude and fixed 800 mA amplitude ECT in older depressed subjects (n = 25 per group, n = 50 total). Relative to fixed 800 mA ECT: H1: Individualized amplitude arm will have improved RUL antidepressant outcome (IDS-C30 response rates and reduced BT electrode placement switch at V2). H2: Individualized amplitude arm will have improved cognitive outcomes (DKEFS-Verbal Fluency

This description comes directly from the study's public registry record.

Talk to the study team

Chris Abbott, MD  ·  5052720406  ·  cabbott@salud.unm.edu

Megan Lloyd, MS  ·  ‭(505) 272-3507‬  ·  meglloyd@salud.unm.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of New Mexico Health Science CenterAlbuquerque, New Mexico, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05699226