Mechanisms Of Change in Psychotherapy: The Effects of Cognitive Behavioral Therapy and Psychodynamic Therapy in Once - Versus Twice - Weekly Sessions on Outcomes in Depression.
MOP II
1 other identifier
interventional
200
1 country
1
Brief Summary
The MOP II study examines how to improve therapy for people struggling with a depressive disorder. Cognitive Behavioral Therapy (CBT) and Short-Term Psychodynamic Psychotherapy (STPP) are two evidence-based treatments for depression that are widely used. Meta-analyses indicate that CBT and STPP are one average equally effective and superior to no treatment. However, many patients do not respond sufficiently and relapse rates after acute phase treatment are high. Earlier research and theoretical insights suggest three promising strategies to enhance the effectiveness of psychotherapy. First, we want to examine whether increasing the frequency of the sessions will increase the effect of therapy. We want to compare once-weekly and twice-weekly sessions in both CBT and STPP to see whether more frequent sessions lead to better and more lasting reductions in depressive symptoms with the same total number of sessions. Second, the study aims to answer what works for whom in two different psychotherapeutic approaches. People with depression differ in personality, life experiences, relationship styles, and how they understand the causes of their depression. Previous findings suggest that patients do better when the therapy approach matches how they see their problems. The MOP II study wants to replicate this finding. Third, the study wants to examine how therapy leads to change. In CBT, improvement is thought to happen through changes in thinking patterns, such as fewer negative automatic thoughts and less rumination. In STPP, change is expected to come from better self-understanding, greater emotional awareness, and healthier ways of relating to others. Consequently, the goal of the MOP II study is to find out whether more frequent therapy, better matching of patients to treatment type, and a clearer understanding of how therapy works can lead to faster improvement of depressive symptoms.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Mar 2026
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 6, 2026
CompletedFirst Posted
Study publicly available on registry
February 13, 2026
CompletedStudy Start
First participant enrolled
March 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2030
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2030
February 18, 2026
February 1, 2026
4.8 years
February 6, 2026
February 13, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Hamilton Depression Rating Scale (HDRS)
Hamilton Depression Rating Scale (HDRS) is a clinician-rated questionnaire used to assess the severity of depressive symptoms. Higher total scores indicate more severe depression.
From enrollment to the end of treatment at 28 weeks
The Patient Health Questionnaire (PHQ-9)
PHQ-9 is a 9-item scale that measures levels of depression. The PHQ-9 is a self assessment instrument and higher scores indicate more severe depressive symptoms
From baseline (enrollment) to end of treatment at 28 weeks
Secondary Outcomes (50)
General Anxiety Disorder
From baseline to end of treatment at 28 weeks
The Work And Social Adjustment Scale (WSAS)
From enrollment to end of treatment at 28 weeks
The Personality Inventory for DSM-5-Brief Form (PID-5-BF)-Adult
From enrollment to end of treatment at 28 weeks
The Level of Personality Functioning Scale-Brief Form (LPFS-BF)
From enrollment to end of treatment at 28 weeks
The Self- Reflection and Insight Scale (SRIS)
From enrollment to end of treatment at 28 weeks
- +45 more secondary outcomes
Study Arms (4)
CBT once weekly
EXPERIMENTALThe patients in this arm will receive CBT once a week in 16 weeks plus three monthly boosters during 3 months
CBT twice weekly
EXPERIMENTALThe patients in this arm will receive CBT twice a week in 8 weeks plus three booster sessions every second week three times.
STPP once weekly
EXPERIMENTALThe patients in this arm will receive STPP once a week in 28 weeks.
STPP twice weekly
EXPERIMENTALThe patients in this arm will receive STPP twice a week in 14 weeks.
Interventions
The patients will receive psychodynamic therapy
The study explores cognitive behavior therapy and psychodynamic therapy
Eligibility Criteria
You may qualify if:
- age 18-65 years
- Major Depressive Disorder Hamilton Depression Rating Scale (HDRS) \> 14.
- Speak and understand a Scandinavian language
- Willingness and ability to give informed consent.
You may not qualify if:
- Current or past neurological illness
- Traumatic brain injury
- Current alcohol and/or substance dependency disorders
- Psychotic disorders
- Bipolar disorders
- Developmental disorders
- IQ \<70.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Oslo University Hospital
Oslo, Norway, Postboks 4959, Norway
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
February 6, 2026
First Posted
February 13, 2026
Study Start
March 1, 2026
Primary Completion (Estimated)
December 31, 2030
Study Completion (Estimated)
December 31, 2030
Last Updated
February 18, 2026
Record last verified: 2026-02