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W05-01 - Rationale and Design of an RCT Comparing “EMC-Strategy” with TAU in Patients with Major Depression - the EMC Trial

Published online by Cambridge University Press:  17 April 2020

A. Tadic
Affiliation:
Department of Psychiatry and Psychotherapy, Germany
S. Gorbulev
Affiliation:
Interdisciplinary Centre for Clinical Trials (IZKS), University Medical Center of the Johannes-Gutenberg University Mainz, Mainz, Germany
N. Dahmen
Affiliation:
Department of Psychiatry and Psychotherapy, Germany Clinic for Psychiatry and Psychotherapy, Katzenelnbogen, Germany
C. Hiemke
Affiliation:
Department of Psychiatry and Psychotherapy, Germany
D.F. Braus
Affiliation:
Clinic for Psychiatry and Psychotherapy, HSK - Dr. Horst-Schmidt-Kliniken, Wiesbaden, Germany
J. Röschke
Affiliation:
Clinic for Psychiatry and Psychotherapy, St. Valentinushaus, Bad Soden, Germany Clinic for Psychiatry and Psychotherapy, St. Valentinushaus, Kiedrich, Germany
D. van Calker
Affiliation:
Dept. of Psychiatry and Psychotherapy, University Medical Center Freiburg, Freiburg im Breisgau, Germany
D. Wachtlin
Affiliation:
Interdisciplinary Centre for Clinical Trials (IZKS), University Medical Center of the Johannes-Gutenberg University Mainz, Mainz, Germany
K. Kronfeld
Affiliation:
Interdisciplinary Centre for Clinical Trials (IZKS), University Medical Center of the Johannes-Gutenberg University Mainz, Mainz, Germany
T. Gorbauch
Affiliation:
Interdisciplinary Centre for Clinical Trials (IZKS), University Medical Center of the Johannes-Gutenberg University Mainz, Mainz, Germany
M. Seibert-Grafe
Affiliation:
Interdisciplinary Centre for Clinical Trials (IZKS), University Medical Center of the Johannes-Gutenberg University Mainz, Mainz, Germany
K. Lieb
Affiliation:
Department of Psychiatry and Psychotherapy, Germany

Abstract

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Introduction

For Major Depression, current guidelines recommend treatment durations of 3-8 weeks until optimisation in case of insufficient outcome. Many retrospective studies indicate that improvement (HAMD-17 decrease ≥20%) occurs usually within 10-14 days and that non-improvement after 14 days of treatment is highly predictive for poor clinical outcome.

Methods

In level 1 of the EMC trial, non-improvers after 14 days of antidepressant treatment will be randomised to “early medication change” (EMC) strategy or treatment according to current guidelines (TAU). EMC schedules treatment optimisations on day 15 and day 29 in case of non-improvement. TAU schedules a medication change after 28 days in case of non-response (HAMD-17 decrease < 50%). Both interventions will last 42 days. In levels 2 and 3, EMC strategies will be compared with TAU strategies in improvers on day 14, who experience a stagnation of improvement during the course of treatment. The EMC trial is a multi-centre, multi-step, randomised controlled trial investigating for the first time prospectively, whether non-improvers after 14 days of antidepressant treatment with EMC are more likely to attain remission on treatment day 56 compared to patients with TAU. The trial is funded by the German Federal Ministry of Education and Research (BMBF), will be conducted in cooperation with the BMBF supported Interdisciplinary Centre for Clinical Trials (IZKS) Mainz and at six trial sites in Germany.

Results/conclusions

If the EMC strategy leads to significantly more remitters, consecutive revision of guidelines, clinical practice and research settings for the treatment of MD can be expected.

Type
The antidepressant effect: Onset of action and relation to depression severity
Copyright
Copyright © European Psychiatric Association 2010
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