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A Finnish Community Randomized Psychotherapy Effectiveness Study for Major Depression

Primary Purpose

Depressive Disorder, Major

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Interpersonal Psychotherapy
Psychoeducational Group Therapy
Sponsored by
Helsinki University Central Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depressive Disorder, Major

Eligibility Criteria

18 Years - 64 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Major Depressive Disorder - diagnosed
  • Comorbid anxiety disorders

Exclusion Criteria:

  • Psychosis
  • Suicidal patients
  • Serious acute somatic illness
  • Inability to read and write
  • alcohol dependence or use of illicit drugs

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Active Comparator

    Active Comparator

    No Intervention

    Arm Label

    Interpersonal Psychotherapy

    Psychoeducational Group Therapy

    Treatment as Usual

    Arm Description

    Interpersonal Psychotherapy treatment for MDD patients was implemented with antidepressant pharmacotherapy by national Quidelines for the treatment of Patients with depression. Intervention:Interpersonal psychotherapy as ADD-on method. Outcome was compared with patients in treatment as usual group.

    Psychoeducational Group Therapy arm for MDD patients with antidepressant pharmacotherapy by national Quidelines for the treatment of Patients with depression. Intervention: Psychoeducational Group Treatment as ADD-on method.

    Treatment as usual ( consisting of supportive psychodynamic-oriented treatment) with antidepressant pharmacotherapy by national Quidelines for the treatment of Patients with depression

    Outcomes

    Primary Outcome Measures

    Change from baseline Hamilton Rating Scale for Depression at 12 months

    Secondary Outcome Measures

    Change from baseline Clinical Global Impression, severity and change at 12 months
    Change from baseline Social and Occupational Functioning Assessment Scale at 12 months

    Full Information

    First Posted
    December 4, 2014
    Last Updated
    December 9, 2014
    Sponsor
    Helsinki University Central Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02314767
    Brief Title
    A Finnish Community Randomized Psychotherapy Effectiveness Study for Major Depression
    Official Title
    A Finnish Community Randomized Psychotherapy Effectiveness Study for Major Depression
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2014
    Overall Recruitment Status
    Completed
    Study Start Date
    February 2004 (undefined)
    Primary Completion Date
    April 2007 (Actual)
    Study Completion Date
    April 2007 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Helsinki University Central Hospital

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Lohja Depression Treatment Study is a randomized treatment trial which compares three approaches for treatment of depression:1) Interpersonal Psychotherapy (IPT), 2) Psychoeducational Group Treatment ( PeGT) and 3) Treatment as Usual (TAU). This Trial aims to test and adapt known short term treatment models for Finnish patients and circumstances.
    Detailed Description
    Patients having signs of depression referred to Lohja area secondary level psychiatric clinics were assessed to the trial. After verification the diagnosis of Major Depressive Disorder (MDD) they were informed of the study. Consented patients were randomized to three study arms. Baseline clinical demographics was collected. Psychotherapeutic treatment was implemented by specially trained therapists and the study data was collected by trained psychiatrists who were blinded to the therapy model patients has received.Primary outcome measure was 17-item Hamilton Depression Rating Scale (HAMD) and secondary outcome measures were Clinical Global Impression scale (CGI), Social and Occupational Functioning Assessment Scale ( SOFAS), Social Adaptation Scale ( Finnish translation JES) and Quality of Life assessment ( a Finnish validated questionnaire 15-D).The total of sick leave days and number of possible disability pensions in a year were assessed as well. Assessments were implemented at the beginning, at 1,5 month, at 3 months ( which was the end of active treatment of short-term psychotherapies), at 6 months and at 12 months. The primary assessment was planned to carry out using tests of group comparison. Sample size of 32 and 32 achieve 91% power to detect a clinically meaningful difference with a significance level (alpha) of 0.01 using two-sided two-sample t-test. Baseline differences in demographic variables and the depression measurement across the three treatment groups were tested using chi-square tests and analysis of variance.Likelihood-based inference using linear mixed models were employed to analyze treatment effects, focusing on the time x treatment interaction. Separate analyses assessed IPT-TAU and PeGT-TAU comparisons. All statistical analyses were performed using R. The aim of this study was to get a total of 140-160 patients, about 50 patients on one group.The final number of patients showed to be 134. The statistical calculation was intent-to-treat model with consideration to missing data, because in this kind of natural setting notable attrition was assumed. The training of the therapists and researchers and quality control during assessments was considered and personnel was supervised throughout the study.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Depressive Disorder, Major

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Investigator
    Allocation
    Randomized
    Enrollment
    134 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Interpersonal Psychotherapy
    Arm Type
    Active Comparator
    Arm Description
    Interpersonal Psychotherapy treatment for MDD patients was implemented with antidepressant pharmacotherapy by national Quidelines for the treatment of Patients with depression. Intervention:Interpersonal psychotherapy as ADD-on method. Outcome was compared with patients in treatment as usual group.
    Arm Title
    Psychoeducational Group Therapy
    Arm Type
    Active Comparator
    Arm Description
    Psychoeducational Group Therapy arm for MDD patients with antidepressant pharmacotherapy by national Quidelines for the treatment of Patients with depression. Intervention: Psychoeducational Group Treatment as ADD-on method.
    Arm Title
    Treatment as Usual
    Arm Type
    No Intervention
    Arm Description
    Treatment as usual ( consisting of supportive psychodynamic-oriented treatment) with antidepressant pharmacotherapy by national Quidelines for the treatment of Patients with depression
    Intervention Type
    Behavioral
    Intervention Name(s)
    Interpersonal Psychotherapy
    Intervention Description
    Patients were treated with IPT method, which was an active comparator vs treatment as usual
    Intervention Type
    Behavioral
    Intervention Name(s)
    Psychoeducational Group Therapy
    Intervention Description
    Patients were treated with PeGt method which was an active comparatos vs treatment as usual
    Primary Outcome Measure Information:
    Title
    Change from baseline Hamilton Rating Scale for Depression at 12 months
    Time Frame
    12 months
    Secondary Outcome Measure Information:
    Title
    Change from baseline Clinical Global Impression, severity and change at 12 months
    Time Frame
    12 months
    Title
    Change from baseline Social and Occupational Functioning Assessment Scale at 12 months
    Time Frame
    12 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    64 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Major Depressive Disorder - diagnosed Comorbid anxiety disorders Exclusion Criteria: Psychosis Suicidal patients Serious acute somatic illness Inability to read and write alcohol dependence or use of illicit drugs
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Heikki O Katila, MD Ph.D.
    Organizational Affiliation
    University of Helsinki
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    27153942
    Citation
    Saloheimo HP, Markowitz J, Saloheimo TH, Laitinen JJ, Sundell J, Huttunen MO, A Aro T, Mikkonen TN, O Katila H. Psychotherapy effectiveness for major depression: a randomized trial in a Finnish community. BMC Psychiatry. 2016 May 6;16:131. doi: 10.1186/s12888-016-0838-1.
    Results Reference
    derived

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    A Finnish Community Randomized Psychotherapy Effectiveness Study for Major Depression

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