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Interpersonal Psychotherapy for Depression
This study is currently recruiting participants.
Verified by Linkoeping University, September 2008
Sponsored by: Linkoeping University
Information provided by: Linkoeping University
ClinicalTrials.gov Identifier: NCT00763594
  Purpose

The study investigates the relative efficacy of Interpersonal Psychotherapy and Brief Relational Therapy for Major Depressive Disorder.


Condition Intervention Phase
Major Depressive Disorder
Behavioral: Brief Relational Therapy
Behavioral: Interpersonal Psychotherapy
Phase I
Phase II

MedlinePlus related topics: Depression
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: Randomized Clinical Trial of Interpersonal Psychotherapy and Brief Relational Therapy for Major Depressive Disorder

Further study details as provided by Linkoeping University:

Primary Outcome Measures:
  • Hamilton Depression Rating Scale [ Time Frame: Before treatment, at treatment termination (16 weeks) and at 1 and 2 year follow-up ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Outcome Questionnaire - 45 [ Time Frame: Before treatment, after session 8, at treatment termination (16 weeks) and at 1 and 2 year follow-up ] [ Designated as safety issue: No ]

Estimated Enrollment: 90
Study Start Date: September 2008
Estimated Study Completion Date: December 2014
Estimated Primary Completion Date: December 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
IPT: Active Comparator
Interpersonal Psychotherapy for Major Depressive Disorder
Behavioral: Interpersonal Psychotherapy
16 weeks of Interpersonal Psychotherapy for Major Depressive Disorder
BRT: Experimental
Brief Relational Therapy adapted for treatment of Major Depressive Disorder
Behavioral: Brief Relational Therapy
16 weeks of psychodynamically informed and therapy alliance focussed psychotherapy adapted for treating Major Depressive Disorder.

Detailed Description:

Interpersonal Therapy (IPT; Klerman et al., 1984) and Brief Relational Therapy (BRT; Safran & Muran, 2000) are both brief psychotherapies based on interpersonal theory, but differ mainly in type of relational focus. IPT is mainly focused on helping the patient solve specific interpersonal problems in the patient's life outside therapy that are thought to maintain the patient's depression. At Linköping University the first formal training in IPT in Sweden is given. Therapists are trained for two years in IPT and Brief Relational Therapy (BRT), the latter being a treatment based on attachment theory, relational psychoanalysis and research on ruptures and resolution of the therapeutic alliance. BRT thus resembles IPT in its theoretical roots, but differs in being more focussed on exploration of the therapy relationship than on interpersonal relationships outside therapy. Patients with Major Depressive Disorder are randomized to 16 sessions of either IPT or BRT (slightly modified for depression treatment). All therapists provide both treatments, thus controlling for general therapist effects. Outcome measures include the SCID-I and II, Hamilton Depression Rating Scale, Patient Health Questionnaire - 9, Outcome Questionnaire - 45, Inventory of Interpersonal Problems, Depressive Experiences Questionnaire, Five Facet Mindfulness Inventory and Quality of Life Inventory. In addition, the Adult Attachment Interview will be administered at therapy start, termination and follow-up and scored with the Reflective Functioning Scale. Also, a separate symptom-specific RF scale designed to measure reflection on depressive symptoms is used. Process measures (filled out by both therapist and patient) include the Working Alliance Inventory (12-item version) and the Feeling Checklist, and are scored by both therapist and patient after each session. All sessions, including assessment sessions, are video recorded, allowing for competence ratings and detailed process research. The study fulfils several purposes; it tests BRT against a treatment with already established efficacy and allows for testing hypothesized interaction effects between treatment modality and patient characteristics.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Major Depressive Disorder (DSM-IV)

Exclusion Criteria:

  • Any psychotic disorder
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00763594

Contacts
Contact: Fredrik Falkenstrom, MA +46 155 247935 fredrik.falkenstrom@ll.se
Contact: Rolf Holmqvist, PhD +46 13 28 25 60 rolf.holmqvist@liu.se

Locations
Sweden
Linkoping University Recruiting
Linkoping, Sweden, SE-581 83
Contact: Rolf Holmqvist, PhD     +46 13 28 25 60     rolf.holmqvist@liu.se    
Principal Investigator: Rolf Holmqvist, PhD            
Sponsors and Collaborators
Linkoeping University
Investigators
Principal Investigator: Fredrik Falkenstrom, MA Sormland County Council, Linkoping University
  More Information

No publications provided

Responsible Party: Linkoeping University, Sormland County Council ( Fredrik Falkenstrom )
Study ID Numbers: M59-08
Study First Received: September 30, 2008
Last Updated: November 18, 2008
ClinicalTrials.gov Identifier: NCT00763594  
Health Authority: Sweden: Regional Ethical Review Board

Keywords provided by Linkoeping University:
Major Depression
Interpersonal Psychotherapy
Brief Relational Therapy
Outcome research

Study placed in the following topic categories:
Depression
Mental Disorders
Mood Disorders
Depressive Disorder, Major
Depressive Disorder
Behavioral Symptoms

Additional relevant MeSH terms:
Pathologic Processes
Disease

ClinicalTrials.gov processed this record on February 12, 2009