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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02538835
Other study ID # 46332
Secondary ID
Status Not yet recruiting
Phase N/A
First received August 31, 2015
Last updated November 14, 2016
Start date August 2018

Study information

Verified date November 2016
Source University of Southern Denmark
Contact Mette E Andersen, PhD
Phone 65504625
Email melandersen@health.sdu.dk
Is FDA regulated No
Health authority Denmark: The National Committee on Health Research Ethics
Study type Interventional

Clinical Trial Summary

This study evaluates the effect of metacognitive group therapy on depression compared to mindfulness groups and supportive groups. The participants, all with a history of depression and with current symptoms of depression, will be randomized to one of the three group interventions.


Description:

Metacognitive therapy (MCT) show promising results in alleviating depressive symptoms and reducing relapse of depression. However studies of MCT as a group intervention is limited and higher quality studies of the effectiveness of MCT is warranted. The present study aim to produce more conclusive evidence on the effect of MCT comparing MCT in groups with both and active control group and mindfulness based cognitive therapy (MBCT), which together with pharmacotherapy is currently one of the preferred treatment choices. Currently pharmacotherapy, cognitive therapy and MBCT seem to help 40-58% of the patients efficiently. The current studies of MCT indicate that this intervention may help a higher proportion of the patients.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 165
Est. completion date
Est. primary completion date July 2020
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Consent to participate

- History of clinical depression

- Current depressive symptoms

- Verbal and cognitive abilities to complete the questionnaires during the study

- Stable medication - if any medication is ordinated

- Speaks fluently danish

Exclusion Criteria:

- If criteria for psychosis, bipolar disorder or personality disorder is matched

- known brain damage or mental retardation

- substance abuse

- women who are pregnant or breast feeding

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Metacognitive therapy
Group format, 10-12 participants in each group. 8 weekly sessions of two hours each.
Mindfulness based cognitive therapy, group
Group format, 10-12 participants in each group. 8 weekly sessions of two hours each following the manual described by Williams, Zindel & Segal.
Support groups
Group format, 10-12 participants in each group. The sessions will only be of supportive character and will not focus on changing or restructuring thoughts, scripts or thought patterns. The format will follow a manual but compared to the other intervention groups the format allow participants to suggests themes for discussions.

Locations

Country Name City State
Denmark University of Southern Denmark Odense Southern Denmark

Sponsors (2)

Lead Sponsor Collaborator
University of Southern Denmark Center for Kognitive Terapier og Supervision

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline on Hamilton depression scale 8 weeks No
Primary Change from baseline on Hamilton depression scale 32 weeks No
Secondary Change from baseline on Becks depression inventory 8 weeks No
Secondary Change from baseline on Becks depression inventory 32 weeks No
Secondary Change from baseline on Becks Anxiety Inventory 8 weeks No
Secondary Change from baseline on Becks Anxiety Inventory 32 weeks No
Secondary Change from baseline on Ruminative Response Scale 8 weeks No
Secondary Change from baseline on Ruminative Response Scale 32 weeks No
Secondary Change from baseline on Metacognitive questionnaire 8 weeks No
Secondary Change from baseline on Metacognitive questionnaire 32 weeks No
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