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Evaluation of Three Continuation Therapies After ECT Concerning Efficacy and Cognition in Severly Depressed Patients (EffECT)

Primary Purpose

Depression, Major Depression

Status
Completed
Phase
Phase 1
Locations
Germany
Study Type
Interventional
Intervention
TCAs, SSRIs, NARIs, SNRIs, Lithium
Electroconvulsive therapy
Cognitive behavioral group therapy
Sponsored by
Charite University, Berlin, Germany
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression focused on measuring therapy resistant depression, severe depression

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Major depressive episode (unipolar)
  • Response to acute ECT (at least 50% reduction in HAMD)
  • Capacity to consent
  • Sufficient comprehension of the German language

Exclusion Criteria:

  • Schizophrenia, schizoaffective disorder, or other psychosis
  • Amnestic disorder, dementia, or delirium
  • Pregnancy
  • Epilepsy
  • Current alcohol or substance abuse or dependence
  • CNS disease or brain injury not associated with psychotropic drug exposure
  • ECT in the past 3 months
  • Acute suicidality
  • Judiciary hospitalization

Sites / Locations

  • Department of Psychiatry, Charité University Medicine, Campus Benjamin Franklin, Berlin, Germany

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

1

2

3

Arm Description

Continuation-Medication with Antidepressants (after WBS Guidelines)

Continuation-ECT with Antidepressants

Continuation-Psychotherapy (Cognitive Behavioral Group Psychotherapy including the "Situational Analysis" of CBASP)

Outcomes

Primary Outcome Measures

Score on HAMD after 6 and 12 months

Secondary Outcome Measures

Relapse rate after 6 and 12 months
Response and remission rates after 6 and 12 months
Scores on MADRS, BDI, and CGI after 6 and 12 months

Full Information

First Posted
February 20, 2007
Last Updated
November 8, 2011
Sponsor
Charite University, Berlin, Germany
Collaborators
German Research Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00437385
Brief Title
Evaluation of Three Continuation Therapies After ECT Concerning Efficacy and Cognition in Severly Depressed Patients
Acronym
EffECT
Official Title
Phase 1 Study: Evaluation of Three Continuation Therapies After Acute Electroconvusive Therapy (ECT) Concerning Efficacy and Cognition in Severly Depressed Patients
Study Type
Interventional

2. Study Status

Record Verification Date
November 2011
Overall Recruitment Status
Completed
Study Start Date
March 2005 (undefined)
Primary Completion Date
March 2010 (Actual)
Study Completion Date
March 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Charite University, Berlin, Germany
Collaborators
German Research Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate three different continuation treatments after acute ECT concerning efficacy and impact on cognition in severly depressed patients.
Detailed Description
BACKGROUND While electroconvulsive therapy (ECT) in major depression is effective, high relapse rates and cognitive effects limit its long-term use. Continuation treatment after ECT with combinations of C-ECT or psychotherapy and medication may decrease relapse rates and cognitive side effects while changing cognitive psychological variables like dysfunctional attitudes in the long-term. CENTRAL RESEARCH QUESTIONS Evaluation of the efficacy of three continuation treatments aimed at preventing relapses after acute ECT Examination of the cognitive side effects and the changes of cognitive psychological variables during acute and continuation treatment METHODS In a prospective, randomized, controlled, long-term study we assign 60 depressed ECT responder either to antidepressant treatment alone, or C-ECT plus medication, or cognitive behavioral group therapy plus medication. Depressive symptoms and cognition were assessed before, during, immediately after acute ECT and two, four, six, and 12 months during continuation therapy. HYPOTHESES It is hypothesized that the use of combination continuation therapies after effective ECT leads to lower HAMD scores and lower relapse rates than the standard treatment with antidepressants alone after 6 months. In addition, we assume that the CBT group will establish more functional macro-patterns than the somatic treatments in the long term and will have the lowest HAMD scores and relapse rates after 1 year. With regard to the cognitive side effects, the autobiographical memory is expected to be the only specific part of memory being affected negatively by ECT in the short and long term.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Major Depression
Keywords
therapy resistant depression, severe depression

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Continuation-Medication with Antidepressants (after WBS Guidelines)
Arm Title
2
Arm Type
Experimental
Arm Description
Continuation-ECT with Antidepressants
Arm Title
3
Arm Type
Experimental
Arm Description
Continuation-Psychotherapy (Cognitive Behavioral Group Psychotherapy including the "Situational Analysis" of CBASP)
Intervention Type
Drug
Intervention Name(s)
TCAs, SSRIs, NARIs, SNRIs, Lithium
Intervention Description
Antidepressant, dosage, and duration are chosen due to the guidelines of the WFSBP (Bauer et al. 2002)
Intervention Type
Procedure
Intervention Name(s)
Electroconvulsive therapy
Intervention Description
ECT treatment is administered three times per week on non-successive weekdays and according to existing standards. Treatment lasts for at least three weeks (nine ECT sessions). Psychopharmacological treatment is continued during ECT treatment. Patients receive ultrabrief pulse (0.3 ms), unilateral treatment at a frequency of 40-100 Hertz. Stimulation is applied to the non-dominant hemisphere, according to the d'Elia electrode positioning paradigm. All patients are initially treated with right unilateral stimulation and in case of non-response switched to bilateral treatment. Stimulus intensity is chosen according to individual seizure threshold and administered at 2.5 to 6-fold intensity. During the ECT session, patients are anesthetized, under the influence of a muscle relaxant, and monitored regarding their vital functions.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive behavioral group therapy
Intervention Description
The continuation-psychotherapy (continuation cognitive behavioral therapy, C-CBT) sample took part in a newly developed cognitive behavioral group therapy program called "EffECTive". This therapy program was developed within the EffECT-project (Brakemeier et al. 2005), to fit the specific target group of patients finished with acute ECT-treatment. EffECTive is a group therapy that combines several aspects of existing cognitive-behavioral depression manuals with new elements (e.g., the situational analysis from CBASP, McCullough 2000), to fit the target group. Therapy sessions were held once a week and include approximately 15 sessions until follow-up.
Primary Outcome Measure Information:
Title
Score on HAMD after 6 and 12 months
Time Frame
6 and 12 months after enetering continuation phase
Secondary Outcome Measure Information:
Title
Relapse rate after 6 and 12 months
Time Frame
6 and 12 months after enetering continuation phase
Title
Response and remission rates after 6 and 12 months
Time Frame
6 and 12 months after enetering continuation phase
Title
Scores on MADRS, BDI, and CGI after 6 and 12 months
Time Frame
6 and 12 months after enetering continuation phase

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Major depressive episode (unipolar) Response to acute ECT (at least 50% reduction in HAMD) Capacity to consent Sufficient comprehension of the German language Exclusion Criteria: Schizophrenia, schizoaffective disorder, or other psychosis Amnestic disorder, dementia, or delirium Pregnancy Epilepsy Current alcohol or substance abuse or dependence CNS disease or brain injury not associated with psychotropic drug exposure ECT in the past 3 months Acute suicidality Judiciary hospitalization
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Malek Bajbouj, PhD
Organizational Affiliation
Department of Psychiatry, Charité University Medicine, Campus Benjamin Franklin, Berlin, Germany
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Eva-Lotta Brakemeier, MA
Organizational Affiliation
Department of Psychiatry and Psychotherapy, University Medicine, Freiburg, Germany
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Norbert Kathmann, PhD
Organizational Affiliation
Department of Clinical Psychology, Humboldt-University, Berlin, Germany
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Psychiatry, Charité University Medicine, Campus Benjamin Franklin, Berlin, Germany
City
Berlin
ZIP/Postal Code
14050
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
11255384
Citation
Sackeim HA, Haskett RF, Mulsant BH, Thase ME, Mann JJ, Pettinati HM, Greenberg RM, Crowe RR, Cooper TB, Prudic J. Continuation pharmacotherapy in the prevention of relapse following electroconvulsive therapy: a randomized controlled trial. JAMA. 2001 Mar 14;285(10):1299-307. doi: 10.1001/jama.285.10.1299.
Results Reference
background
PubMed Identifier
10839336
Citation
Lisanby SH, Maddox JH, Prudic J, Devanand DP, Sackeim HA. The effects of electroconvulsive therapy on memory of autobiographical and public events. Arch Gen Psychiatry. 2000 Jun;57(6):581-90. doi: 10.1001/archpsyc.57.6.581.
Results Reference
background
PubMed Identifier
17146008
Citation
Kellner CH, Knapp RG, Petrides G, Rummans TA, Husain MM, Rasmussen K, Mueller M, Bernstein HJ, O'Connor K, Smith G, Biggs M, Bailine SH, Malur C, Yim E, McClintock S, Sampson S, Fink M. Continuation electroconvulsive therapy vs pharmacotherapy for relapse prevention in major depression: a multisite study from the Consortium for Research in Electroconvulsive Therapy (CORE). Arch Gen Psychiatry. 2006 Dec;63(12):1337-44. doi: 10.1001/archpsyc.63.12.1337.
Results Reference
background
PubMed Identifier
24462229
Citation
Brakemeier EL, Merkl A, Wilbertz G, Quante A, Regen F, Buhrsch N, van Hall F, Kischkel E, Danker-Hopfe H, Anghelescu I, Heuser I, Kathmann N, Bajbouj M. Cognitive-behavioral therapy as continuation treatment to sustain response after electroconvulsive therapy in depression: a randomized controlled trial. Biol Psychiatry. 2014 Aug 1;76(3):194-202. doi: 10.1016/j.biopsych.2013.11.030. Epub 2013 Dec 12. Erratum In: Biol Psychiatry. 2014 Sep 1;76(5):430.
Results Reference
derived

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Evaluation of Three Continuation Therapies After ECT Concerning Efficacy and Cognition in Severly Depressed Patients

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