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Early Integrated Intervention in Severe Affective Disorders

Primary Purpose

Depressive Disorder, Bipolar Disorder

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Prophylactic combined medical and psychological treatment
Sponsored by
Hovedstadens Sygehusfaelesskab
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depressive Disorder focused on measuring Prophylactic treatment, Pharmacological treatment, Psychological treatment

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: 1. Discharge diagnosis of severe single depressive episode, recurrent depression, manic/mixed episode or bipolar disorder Exclusion Criteria: Moderate to severe dementia Incapable in understanding or reading danish Earlier randomised to the trial

Sites / Locations

  • Department of Psychiatry, University Hospital of Copenhagen, Denmark

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

A,2

A, 1

Arm Description

Standard treatment: treatment as usual at a community psychiatric center, private psychiatrist or general practitioner.

Behavioral: Prophylactic combined medical and psychological treatment Medical treatment is naturalistic and evidence based according to international recommendations. Psychological treatment is either group psychoeducation or group cognitive behavioural therapy.

Outcomes

Primary Outcome Measures

Time to re-admission

Secondary Outcome Measures

Time to recurrence of an affective episode (depressive (MDI) or manic/mixed (MDQ)).

Full Information

First Posted
November 14, 2005
Last Updated
March 18, 2015
Sponsor
Hovedstadens Sygehusfaelesskab
Collaborators
Rigshospitalet, Denmark, Hvidovre University Hospital, Amager Hospital, Frederiksberg University Hospital, Bispebjerg Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00253071
Brief Title
Early Integrated Intervention in Severe Affective Disorders
Official Title
Early Integrated Intervention in Severe Affective Disorders - a Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2015
Overall Recruitment Status
Completed
Study Start Date
December 2005 (undefined)
Primary Completion Date
March 2012 (Actual)
Study Completion Date
March 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hovedstadens Sygehusfaelesskab
Collaborators
Rigshospitalet, Denmark, Hvidovre University Hospital, Amager Hospital, Frederiksberg University Hospital, Bispebjerg Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether early integrated prophylactic combined medical and psychological outpatient treatment is associated with a better prognosis in patients with severe unipolar and bipolar affective disorders than standard treatment.
Detailed Description
Patients who have been hospitalised for unipolar or bipolar disorder have a poor prognosis with highly increased risk of recurrence of episodes and increased risk of psychosocial dysfunction. It seems as integrated prophylactic combined medical and psychological out-patient treatment may lead to a better long-term prognosis in patients with affective disorders in general. It has not been specifically investigated whether such integrated treatment may improve long-term outcome if the intervention is offered early in the course of the affective illness. Subjects: Patients currently discharged from first, second or third hospitalisation ever from psychiatric department with a diagnosis of severe single depressive episode/recurrent depression or with a diagnosis of manic/mixed episode or bipolar disorder. Comparison: Early intervention with integrated prophylactic combined medical and psychological outpatient treatment as offered by a clinic for affective disorders compared with standard outpatient treatment as offered by community psychiatric centres, private specialists in psychiatry or general practitioners.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depressive Disorder, Bipolar Disorder
Keywords
Prophylactic treatment, Pharmacological treatment, Psychological treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
426 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A,2
Arm Type
Active Comparator
Arm Description
Standard treatment: treatment as usual at a community psychiatric center, private psychiatrist or general practitioner.
Arm Title
A, 1
Arm Type
Experimental
Arm Description
Behavioral: Prophylactic combined medical and psychological treatment Medical treatment is naturalistic and evidence based according to international recommendations. Psychological treatment is either group psychoeducation or group cognitive behavioural therapy.
Intervention Type
Behavioral
Intervention Name(s)
Prophylactic combined medical and psychological treatment
Intervention Description
Medical treatment is naturalistic and evidence based according to international recommendations. Psychological treatment is either group psychoeducation or group cognitive behavioural therapy.
Primary Outcome Measure Information:
Title
Time to re-admission
Time Frame
0-6 years
Secondary Outcome Measure Information:
Title
Time to recurrence of an affective episode (depressive (MDI) or manic/mixed (MDQ)).
Time Frame
1 and 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1. Discharge diagnosis of severe single depressive episode, recurrent depression, manic/mixed episode or bipolar disorder Exclusion Criteria: Moderate to severe dementia Incapable in understanding or reading danish Earlier randomised to the trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lars V kessing, Professor
Organizational Affiliation
Department of psychiatry, University Hospital of Copenhagen, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Psychiatry, University Hospital of Copenhagen, Denmark
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
24268595
Citation
Kessing LV, Hansen HV, Christensen EM, Dam H, Gluud C, Wetterslev J; Early Intervention Affective Disorders (EIA) Trial Group. Do young adults with bipolar disorder benefit from early intervention? J Affect Disord. 2014 Jan;152-154:403-8. doi: 10.1016/j.jad.2013.10.001. Epub 2013 Oct 10.
Results Reference
derived
PubMed Identifier
23349295
Citation
Kessing LV, Hansen HV, Hvenegaard A, Christensen EM, Dam H, Gluud C, Wetterslev J; Early Intervention Affective Disorders (EIA) Trial Group. Treatment in a specialised out-patient mood disorder clinic v. standard out-patient treatment in the early course of bipolar disorder: randomised clinical trial. Br J Psychiatry. 2013 Mar;202(3):212-9. doi: 10.1192/bjp.bp.112.113548. Epub 2013 Jan 24.
Results Reference
derived
PubMed Identifier
22442673
Citation
Hansen HV, Christensen EM, Dam H, Gluud C, Wetterslev J, Kessing LV; Early Intervention Affective Disorders (EIA) Trial Group. The effects of centralised and specialised intervention in the early course of severe unipolar depressive disorder: a randomised clinical trial. PLoS One. 2012;7(3):e32950. doi: 10.1371/journal.pone.0032950. Epub 2012 Mar 19.
Results Reference
derived
PubMed Identifier
21291564
Citation
Kessing LV, Hansen HV, Christensen EM, Dam H, Gluud C, Wetterslev J; Early Intervention Affective Disorders (EIA) Group. The effects of centralised and specialised combined pharmacological and psychological intervention compared with decentralised and non-specialised treatment in the early course of severe unipolar and bipolar affective disorders--design of two randomised clinical trials. Trials. 2011 Feb 3;12:32. doi: 10.1186/1745-6215-12-32.
Results Reference
derived

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Early Integrated Intervention in Severe Affective Disorders

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