MedTrace Logo

Early Integrated Intervention in Severe Affective Disorders

NCT00253071 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 426

Last updated 2015-03-19

No results posted yet for this study

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.

Conditions

Interventions

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.

Sponsors & Collaborators

  • Rigshospitalet, Denmark

    collaborator OTHER

  • Hvidovre University Hospital

    collaborator OTHER

  • Amager Hospital

    collaborator OTHER

  • Frederiksberg University Hospital

    collaborator OTHER

  • Bispebjerg Hospital

    collaborator OTHER

  • Hovedstadens Sygehusfaelesskab

    lead OTHER

Principal Investigators

  • Lars V kessing, Professor · Department of psychiatry, University Hospital of Copenhagen, Denmark

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-12-31
Primary Completion
2012-03-31
Completion
2012-03-31

Countries

  • Denmark

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00253071 on ClinicalTrials.gov