Group Metacognitive Therapy vs Clinical Management for Depression

Major Depressive Disorder Clinical Trial

Official title:

A Randomized Controlled Trial of the Effectiveness of Group Metacognitive Therapy vs Clinical Management for Patients With Major Depressive Disorder

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03711123
• Other study ID #: 2015/673-1
• Status: Recruiting
• Phase: N/A
• Start date: November 1, 2018
• Est. completion date: June 2025

Study information

• Verified date: October 2018
• Source: University of Oslo
• Contact: Toril Dammen, PhD
• Phone: 4790163433
• Email: toril.dammen[@]medisin.uio.no
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The main aims of the study are to (1) compare the effectiveness of Group metacognitive therapy (GMCT) treatment to that of clinical management and (2) explore patterns of change and investigate factors associated with treatment outcome

Description:

Major depressive disorder (MDD) is a disabling condition which adversely affects a person's family, work or school life, sleeping and eating habits, and general health.

Cognitive-behavioral therapy (CBT) is a well established effective recommended treatment for MDD. However, only 40-58 % of patients receiving CBT may be classified as recovered using clinical significant change assessed by the Beck Depression Inventory and only between one-third and one quarter of patients receiving CBT remain recovered 18 months after treatment.

A new treatment approach to MDD is Metacognitive Therapy (MCT). In this treatment approach, MDD is conceptualized as being maintained by rumination and meta-cognitions. Treatment seeks to challenge and change specific meta-cognitions and rumination, through behavioural experiments and verbal reattribution. There is accumulating evidence that MCT is effective in the treatment of depression, both individualized and in Groups. A recent pilot study indicated effectiveness above that of CBT. However, the results need to be tested in a randomized controlled trial with a larger sample of patients and a comparison group of active treatment.

The purpose of this trial is to evaluate the effectiveness of Group MCT treatment compared to clinical management included guided self-help and to explore which factors that are associated with depressive symptom outcome in terms of psychological factors, biomarker in terms of heart rate variabilities and polygenic risk score.

The study will be a randomized controlled, trial comprising 64 patients with a primary diagnosis of major depressive disorder (DSM-IV; American Psychiatric Association (APA), 1994). Experienced diagnosticians will assess all patients by using structural interviews such as Structured Clinical Interview for DSM-IV, axis I(SCID I), and axis II disorders (SCID II) and the Hamilton Rating Scale for Depression (HDRS).

All patients will be randomized in blocks to two groups in order to compare the following conditions: Group MCT of 10 weekly sessions lasting 90 minutes and a clinical management condition With 10 weekly individualized sessions up to 60 minutes duration.

Both between-subjects and within-subjects comparisons will be conducted. The research trial will be conducted at an outpatient specialist practice in Drammen, Norway.

The treatment will be administered according to the originators published treatment protocols for MCT for depression. Independent assessors will assess adherence and quality of treatment.

Independent experts will assess the quality of treatment by inspection of a sampling of video-recorded treatments. Using checklists session-by-session will ensure adherence of the therapy. Responsible investigator and supervisors will be using video of all treatment sessions to assess adherence to the treatment condition.

All patients referred for the study will be consecutively assessed at intake (SCID-I + II, HDRS-17). Based on diagnosis and criteria for inclusion and exclusion, the patients will be asked to volunteer to participate in the study and confirm by signing a form of consent.

Patients will be randomized to one of two conditions. Patients will be asked to self-rate symptoms on a battery of self-report questionnaires.

The patients will be assessed prior to treatment, by 10 weeks in treatment, and at six months and at one and two years of follow-up.

Reassessment of the diagnosis and symptom severity is made by post-treatment.

Criteria for recovery will be: Jacobsen criteria of a minimum change and patients crossing the cut-off point on two measures: The HDRS-17 and Beck Depression Inventory (BDI). Other outcome measures will include:

Reduction of depressive symptoms as measured by self-report questionnaires Number of patients with no MDD diagnosis based on SCID-I after treatment Relapse rate during six months and at one and two years follow-up The proportion of responders as measured by the HDRS-17 and BDI and those who no longer fulfil the conditions for a MDD diagnosis after 10 weeks (post-treatment) and by 6 months and one and two years follow-up.

The secondary efficacy variables will be the proportion of responders at 10 weeks (post-treatment) and six months and by one and two years follow-up as measured by the other symptom measures.

A comparison between the two groups of patients will be conducted at 10 weeks (post-treatment) and there will be 6 month and at one- and two years.

A within group analyses will be conducted in order to estimate effect sizes and significant clinical change estimates.

A computer provided by University of Oslo (UiO) will generate the randomization list.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 64
• Est. completion date: June 2025
• Est. primary completion date: April 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• MDD is primary problem

• 18-65 years

• stable on medication for at least 8 weeks or medication free

• able to understand and write the Norwegian Language

• signed written informed consent prior to participation

Exclusion Criteria:

• Medical or physical condition underlying depression

• psychosis or organic mental illness

• current suicide intent

• not willing to Accept no changes in medication during treatment

• not willing to Accept random allocation

• cluster A or cluster B personality disorder

• alcohol/substance dependence/abuse

• concurrent psychological treatment or evidence based psychotherapy for depression past year

• bipolar disorder

Related Conditions & MeSH terms

• Depression
• Depressive Disorder
• Depressive Disorder, Major
• Major Depressive Disorder

Intervention

Behavioral:
• Group metacognitive therapy
10 weekly Group session of 90 minutes duration
• Clinical management
10 weekly individual sessions With clinical management including guided self-help

Locations

Country	Name	City	State
Norway	Specialist practice Dr Toril Dammen	Drammen	Buskerud

Sponsors (1)

Lead Sponsor	Collaborator
University of Oslo

Country where clinical trial is conducted

Norway, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in depression	Beck Depression Inventory	baseline to 10 weeks (post treatment), 6 months, 12 months and 24 months follow up
Primary	Change in diagnosis	SCID-I	baseline to 10 weeks (post treatment), 6 months, 12 months and 24 months follow up
Primary	Change in depression	Hamilton Depression Rating Scale 17-item version (HDRS-17) yielding total scores from 0 (least severe) to 52 (most severe)	baseline to 10 weeks (post treatment), 6 months, 12 months and 24 months follow up
Secondary	Change in rumination	Ruminative Responses Scale (RRS)	baseline to 10 weeks (post treatment), 6 months, 12 months and 24 months follow up
Secondary	Change in positive beliefs	Positive Beliefs about rumination scale (PBRS)	baseline to 10 weeks, 6 months, 12 months and 24 months follow up
Secondary	Change in Negative beliefs	Negative beliefs about rumination scale (NBRS)	baseline to 10 weeks (post treatment), 6 months, 12 months and 24 months follow up
Secondary	Change in metacognitions	Metacognitions questionnaire-30 (MCQ-30)	baseline to 10 weeks (post treatment), 6 months, 12 months and 24 months follow up
Secondary	Change in personality	Distressed type personality (DS-14)	baseline to 10 weeks (post treatment), 6 months, 12 months and 24 months follow up
Secondary	Change in dysfunctional attitudes and beliefs	Dysfunctional attitude scales (DAS)	baseline to 10 weeks (post treatment), 6 months, 12 months and 24 months follow up
Secondary	Change in resilience	Resilience Scale for adults (RSA)	baseline to 10 weeks (post treatment), 6 months, 12 months and 24 months follow up
Secondary	Change in anxiety	Beck Anxiety Inventory (BAI)	baseline to 10 weeks (post treatment), 6 months, 12 months and 24 months follow up
Secondary	Change in sleep	Pittsburgh sleep quality inventory (PSQI)	baseline to 10 weeks (post treatment), 6 months, 12 months and 24 months follow up
Secondary	change in report of executive function	Behaviour Rating of Executive Function (BRIEF-A)	baseline to 10 weeks (post treatment), 6 months, 12 months and 24 months follow up
Secondary	change in personality diagnoses	SCID-II	baseline to 10 weeks (post treatment), 6 months, 12 months and 24 months follow up