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RecruitingDepressionECTCognitive Change

Amplitude Titration to Improve ECT Clinical Outcomes

Eligible age

50+ yrs

Accepts

All genders

Locations

1 state

Healthy volunteers

No

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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

Sponsor: University of New Mexico

You may qualify if…

  • Diagnosis of major depressive disorder or bipolar II
  • Clinical indications for ECT with right unilateral electrode placement

You may not qualify if…

  • Defined neurological or neurodegenerative disorder (e.g., traumatic brain injury, epilepsy, Alzheimer's disease)
  • Other psychiatric conditions (e.g., schizophrenia, bipolar I disorder)
  • Current drug or alcohol use disorder (except for nicotine)
  • Contraindications to MRI.

Where it's recruiting

New Mexico

Albuquerque

Source: ClinicalTrials.gov · NCT05699226 · last updated 2026-01-26