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ECT Pulse Amplitude and Medial Temporal Lobe Engagement

Primary Purpose

Major Depressive Disorder

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
MECTA Spectrum 5000Q Amplitude
Sponsored by
University of New Mexico
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Major Depressive Disorder focused on measuring electroconvulsive therapy, MRI, major depressive disorder

Eligibility Criteria

50 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Diagnosis of major depressive disorder (with or without psychotic features)
  2. the clinical indications for ECT including treatment resistance or a need for a rapid and definitive response
  3. Hamilton Depression Rating Scale 24-item (HDRS-24) > 21
  4. age range between 50 and 80 years of age
  5. right-handedness

Exclusion Criteria:

  1. Defined neurological or neurodegenerative disorder (e.g., history of head injury with loss of consciousness > 5 minutes, epilepsy, Alzheimer's disease)
  2. other psychiatric conditions (e.g., schizophrenia, schizoaffective disorder, bipolar disorder)
  3. current drug or alcohol use disorder, except for nicotine; and 4) contraindications to MRI.

Sites / Locations

  • Chris Abbott

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

600 mA Right Unilateral ECT

700 mA Right Unilateral ECT

800 mA Right Unilateral ECT

Arm Description

MECTA Spectrum 5000Q Amplitude

MECTA Spectrum 5000Q Amplitude

MECTA Spectrum 5000Q Amplitude

Outcomes

Primary Outcome Measures

Depression Severity
Hamilton Depression Rating Scale - 24 item. Scores range from 0 to 76 (higher scores indicate more depression severity)
Cognition
Hopkins Verbal Learning Trial-Revised (percent retention score, range 0 - 100, higher is better)

Secondary Outcome Measures

Full Information

First Posted
August 16, 2016
Last Updated
June 30, 2023
Sponsor
University of New Mexico
Collaborators
The Mind Research Network, University of Texas, National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT02999269
Brief Title
ECT Pulse Amplitude and Medial Temporal Lobe Engagement
Official Title
ECT Pulse Amplitude and Medial Temporal Lobe Engagement
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
October 2016 (undefined)
Primary Completion Date
March 23, 2020 (Actual)
Study Completion Date
March 23, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of New Mexico
Collaborators
The Mind Research Network, University of Texas, National Institute of Mental Health (NIMH)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Electroconvulsive therapy (ECT) remains the gold-standard treatment for patients with depressive episodes. During a typical four-week ECT series, most depressive episodes will respond to treatment and people will improve their level of functioning (return to work or family). Independent of the antidepressant effect of ECT, many patients experience transient memory impairment. This investigation will examine the impact of one ECT parameter (pulse amplitude or current) on brain changes (structure of connections within the brain) and clinical outcomes. The goal of this investigation is to determine the optimal parameter for an individual patient that will maintain the clinical response (reduce depression severity) and minimize side effects (eliminate memory issues related to treatment).
Detailed Description
Electroconvulsive therapy (ECT) remains the gold-standard treatment for patients with depressive episodes. During a typical four-week ECT series, most depressive episodes remit, and formerly suicidal or psychotically depressed patients will resume their premorbid levels of functioning. Independent of the antidepressant effect of ECT, many patients experience debilitating but transient cognitive effects such as attention and memory deficits. These unwanted side effects are particularly troubling for older patients who are more likely to have existing cognitive deficits. Both the stimulus delivery (electrode placement, pulse amplitude, and pulse width) and seizure induction appear to work in synergy, but the underlying mechanism of action for successful response has yet to be fully elucidated. Moreover, further work is needed to understand the relationship between clinical improvement and cognitive impairment. This investigation will examine the clinical and neurocognitive impact of targeted medial temporal lobe engagement as a function of pulse amplitude, one of several variable factors influencing the ECT charge. The ECT charge is measured in millicoulombs (mC) and derived from multiplying pulse train duration, pulse-pair frequency, pulse width, and pulse amplitude. Pulse amplitude determines the induced electric field strength in the brain and is presently fixed at 900 milliamperes (mA) with no clinical or scientific justification. The central hypothesis of this investigation is that the optimal pulse amplitude for an individual patient will enhance neuroplasticity (clinical response) while minimizing the disruption of dominant hemisphere hippocampal cognitive circuitry (resulting in cognitive stability). The preliminary data informs the dosage range between 600 and 800 mA. Pulse amplitudes outside of this range compromise efficacy (500 mA) or may increase risk of cognitive impairment (900 mA). The first aim of this investigation will identify the electric field strength and neuroplasticity associated with clinical response. Critically, this aim will establish the neuroplasticity threshold, which is defined as the electric field strength necessary to induce neuroplasticity. The second aim will detect the neural correlates of ECT-mediated cognitive changes, which may be related to disrupted dominant hemisphere long-term potentiation. The third aim will use data-driven dual regression to predict the optimal pulse amplitude for an individual patient. This contribution will be significant because the electric field, when manipulated by pulse amplitude, can subsequently maximize hippocampal neuroplasticity (efficacy) and minimize disrupted connectivity (cognitive stability) thus improving clinical outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder
Keywords
electroconvulsive therapy, MRI, major depressive disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Subjects randomized to right unilateral ECT with 600, 700, or 800 mA pulse amplitude.
Masking
ParticipantOutcomes Assessor
Masking Description
Double-blind (participant and outcomes assessor)
Allocation
Randomized
Enrollment
62 (Actual)

8. Arms, Groups, and Interventions

Arm Title
600 mA Right Unilateral ECT
Arm Type
Experimental
Arm Description
MECTA Spectrum 5000Q Amplitude
Arm Title
700 mA Right Unilateral ECT
Arm Type
Experimental
Arm Description
MECTA Spectrum 5000Q Amplitude
Arm Title
800 mA Right Unilateral ECT
Arm Type
Active Comparator
Arm Description
MECTA Spectrum 5000Q Amplitude
Intervention Type
Device
Intervention Name(s)
MECTA Spectrum 5000Q Amplitude
Intervention Description
Current
Primary Outcome Measure Information:
Title
Depression Severity
Description
Hamilton Depression Rating Scale - 24 item. Scores range from 0 to 76 (higher scores indicate more depression severity)
Time Frame
post-ECT Hamilton Depression Rating Scale -24 item. The time frame is 4 weeks after study initiation.
Title
Cognition
Description
Hopkins Verbal Learning Trial-Revised (percent retention score, range 0 - 100, higher is better)
Time Frame
post-ECT Hopkins Verbal Learning Trial-Revised (percent retention score, range 0 - 100, higher is better). The time frame is 4 weeks after study initiation.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of major depressive disorder (with or without psychotic features) the clinical indications for ECT including treatment resistance or a need for a rapid and definitive response Hamilton Depression Rating Scale 24-item (HDRS-24) > 21 age range between 50 and 80 years of age right-handedness Exclusion Criteria: Defined neurological or neurodegenerative disorder (e.g., history of head injury with loss of consciousness > 5 minutes, epilepsy, Alzheimer's disease) other psychiatric conditions (e.g., schizophrenia, schizoaffective disorder, bipolar disorder) current drug or alcohol use disorder, except for nicotine; and 4) contraindications to MRI.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chris Abbott, MD
Organizational Affiliation
University of New Mexico
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chris Abbott
City
Albuquerque
State/Province
New Mexico
ZIP/Postal Code
87131-0001
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
National Data Archive (NDA)
IPD Sharing Time Frame
Clinical, cognitive and MRI data was uploaded to NDA.
IPD Sharing Access Criteria
per NDA protocol
Citations:
PubMed Identifier
32651051
Citation
Abbott CC, Quinn D, Miller J, Ye E, Iqbal S, Lloyd M, Jones TR, Upston J, Deng Z, Erhardt E, McClintock SM. Electroconvulsive Therapy Pulse Amplitude and Clinical Outcomes. Am J Geriatr Psychiatry. 2021 Feb;29(2):166-178. doi: 10.1016/j.jagp.2020.06.008. Epub 2020 Jun 17.
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ECT Pulse Amplitude and Medial Temporal Lobe Engagement

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