NCT07408687

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

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
200

participants targeted

Target at P75+ for not_applicable

Timeline
54mo left

Started Mar 2026

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Study Progress9%
Mar 2026Dec 2030

First Submitted

Initial submission to the registry

February 6, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 13, 2026

Completed
16 days until next milestone

Study Start

First participant enrolled

March 1, 2026

Completed
4.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2030

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2030

Last Updated

February 18, 2026

Status Verified

February 1, 2026

Enrollment Period

4.8 years

First QC Date

February 6, 2026

Last Update Submit

February 13, 2026

Conditions

Keywords

Mechanisms of change in PsychotherapyFrequency of therapy sessions

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

EXPERIMENTAL

The patients in this arm will receive CBT once a week in 16 weeks plus three monthly boosters during 3 months

Behavioral: Cognitive behavior therapy

CBT twice weekly

EXPERIMENTAL

The patients in this arm will receive CBT twice a week in 8 weeks plus three booster sessions every second week three times.

Behavioral: Cognitive behavior therapy

STPP once weekly

EXPERIMENTAL

The patients in this arm will receive STPP once a week in 28 weeks.

Behavioral: Psychodynamic therapy

STPP twice weekly

EXPERIMENTAL

The patients in this arm will receive STPP twice a week in 14 weeks.

Behavioral: Psychodynamic therapy

Interventions

The patients will receive psychodynamic therapy

STPP once weeklySTPP twice weekly

The study explores cognitive behavior therapy and psychodynamic therapy

CBT once weeklyCBT twice weekly

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Interventions

Cognitive Behavioral Therapy

Intervention Hierarchy (Ancestors)

Behavior TherapyPsychotherapyBehavioral Disciplines and Activities

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

Locations