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This study will determine whether medications alone or medications and electroconvulsive therapy (ECT) work best to prevent depressive relapse and to improve quality of life for older people with severe mood disorders.
While advances have been made in the acute treatment of geriatric depression, failure to maintain remission following successful treatment remains a major public health problem. In particular, loss of antidepressant response can result in ongoing functional impairment and increased risk of suicide. This is especially salient for severe and/or treatment resistant illness, even after successful ECT. This trial builds upon the work of the Consortium for Research in Electroconvulsive Therapy (CORE) group that showed that continuation ECT and combination pharmacotherapy were equally effective in preventing relapse following response to acute ECT. We are now testing whether combined pharmacotherapy and ECT, individualized according to patient response, will be more effective in maintaining remission in depressed older adults than pharmacotherapy alone. Moving beyond the traditional fixed schedule for continuation ECT, we are introducing a novel Symptom-Titrated Algorithm-Based Longitudinal ECT (STABLE) regimen. The STABLE algorithm ensures that the timing of ECT treatments is based upon clinical need, helping to achieve the dual goals of adequately treating people showing early signs of symptom re-emergence, while preventing the over-treatment of patients who may be in a stable remission. The continuation therapy "usual care" comparator arm is the combination pharmacotherapy of Li plus VLF (PHARM). At 7 sites, 322 patients will receive an acute course of right unilateral (RUL) ECT augmented by standardized medication (Phase I); 188 remitters are randomly assigned to one of the 2 groups and followed for 6 months (Phase II). To balance the amount of clinical contact, the schedule of clinic and telephone ratings will be identical for patients in both the PHARM and STABLE arms. For both groups, relapse is defined as Hamilton Rating Scale for Depression-24 (HRSD24) scores \>21 at two consecutive time points, suicidality, or psychiatric hospitalization.
Age
60 - No limit years
Sex
ALL
Healthy Volunteers
No
Georgia Regents University
Augusta, Georgia, United States
Mayo Clinic
Rochester, Minnesota, United States
Hoboken University Medical Center (MSSM satellite site)
Hoboken, New Jersey, United States
The Zucker Hillside Hospital North Shore-LIJ Health System
Glen Oaks, New York, United States
Icahn School of Medicine at Mount Sinai
New York, New York, United States
Columbia University/New York State Psychiatric Institute
New York, New York, United States
Weill Cornell Medical College
White Plains, New York, United States
Duke University
Durham, North Carolina, United States
Wake Forest University Medical Center
Winston-Salem, North Carolina, United States
University of Texas Southwestern Medical Center at Dallas
Dallas, Texas, United States
Start Date
January 1, 2010
Primary Completion Date
September 1, 2015
Completion Date
March 1, 2016
Last Updated
April 11, 2017
247
ACTUAL participants
lithium and Venlafaxine
DRUG
ECT
PROCEDURE
Lead Sponsor
Icahn School of Medicine at Mount Sinai
Collaborators
NCT07360600
NCT06793397
Data Source & Attribution
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