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Mindfulness Based Cognitive Therapy for Bipolar Disorder (MBCT-BD)

Primary Purpose

Bipolar Disorder

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Mindfulness Based Cognitive Therapy
Usual Care
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bipolar Disorder focused on measuring randomized controlled trial, Mindfulness based cognitive therapy, clinical effectiveness, cost-effectiveness, working mechanisms

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • bipolar I or II disorder
  • having suffered at least two lifetime depressive episodes, either current or in (partial) remission at baseline (according to SCID assessment)
  • Young Mania Rating Scale score < 8

Exclusion Criteria:

  • a manic episode in the 3 months before the start of the trial
  • lifetime diagnosis of schizophrenia or schizoaffective disorder, current substance abuse disorder, organic brain syndrome, antisocial or borderline personality disorder
  • risk of suicide or aggression
  • the presence of a concurrent significant medical condition impeding the ability to participate
  • currently receiving regular psychological therapy
  • previous participation in a MBCT or MBSR course

Sites / Locations

  • Radboud University Nijmegen Medical Center
  • Dimence GGZ
  • Pro Persona
  • Altrecht GGZ

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Mindfulness Based Cognitive Therapy added to usual care

Usual Care

Arm Description

Patients in the MBCT arm will be invited to participate in MBCT added to their usual care.

Usual care will typically consist of pharmacotherapy, psycho-education and self-management interventions (usually with a psychiatric nurse).

Outcomes

Primary Outcome Measures

Inventory of Depressive Symptomatology
A clinican-administered interview assessing the severity of depressive symptoms

Secondary Outcome Measures

Structured Clinical Interview for DSM-IV-TR Disorders
Diagnostic instrument to assess relapse of depressive or (hypo)manic episode
Young Mania Rating Scale
Young Mania Rating Scale (YMRS) Dutch translation. The YMRS is an 11-item clinician-administered rating scale to assess the severity of (hypo)manic symptoms. It was found to be a reliable, valid, and sensitive rating scale to measure the severity of mania (Young et al., 1978). Its total score ranges from 0 (no (hypo)manic symptoms) to 44 (severe manic symptoms).
Young Mania Rating Scale
Young Mania Rating Scale (YMRS) Dutch translation. The YMRS is an 11-item clinician-administered rating scale to assess the severity of (hypo)manic symptoms. It was found to be a reliable, valid, and sensitive rating scale to measure the severity of mania (Young et al., 1978). Its total score ranges from 0 (no (hypo)manic symptoms) to 44 (severe manic symptoms).
Functioning Assessment Short Test
Brief instrument designed to assess the main functioning problems experienced by psychiatric patients, particularly bipolar patients
Functioning Assessment Short Test
Brief instrument designed to assess the main functioning problems experienced by psychiatric patients, particularly bipolar patients
State/Trait Anxiety Inventory
self-report measure for assessing both state and trait levels of anxiety
State/Trait Anxiety Inventory
self-report measure for assessing both state and trait levels of anxiety
Ruminative Response Scale - brooding subscale
Brooding subscale of the extended version of the Ruminative Response Scale (RRS-EXT). The authors reported adequate internal consistency (α = .79) and test-retest stability (α = .62, with a one year time interval) for the brooding subscale, which consists of five items. We select the brooding subscale because over time, brooding, or rumination, has been more strongly related to levels of depression (Treynor et al., 2003). Items are scored between 1 ((almost) never) to 4 ((almost) always and subscale score ranges between 5 and 20. A higher score indicates a higher level of ruminative brooding.
Ruminative Response Scale - brooding subscale
Brooding subscale of the extended version of the Ruminative Response Scale (RRS-EXT). The authors reported adequate internal consistency (α = .79) and test-retest stability (α = .62, with a one year time interval) for the brooding subscale, which consists of five items. We select the brooding subscale because over time, brooding, or rumination, has been more strongly related to levels of depression (Treynor et al., 2003). Items are scored between 1 ((almost) never) to 4 ((almost) always and subscale score ranges between 5 and 20. A higher score indicates a higher level of ruminative brooding.
Five Facet Mindfulness Questionnaire, short form
Self-report measure consisting of 24 items divided into the subscales observing, describing, acting with awareness, non-judging and non-reactivity.
Five Facet Mindfulness Questionnaire, short form
Self-report measure consisting of 24 items divided into the subscales observing, describing, acting with awareness, non-judging and non-reactivity.
Self-Compassion Scale
Self-Compassion Scale - short form (SCS-SF). The present study will use the 12-item Dutch short-form version of the SCS-SF to measure self-compassion. The scale consists of six components, including self-kindness, self-judgment, common humanity, isolation, mindfulness and over-identification. The SCS-SF has good reliability and validity (Raes et al., 2011). In the short form, each scale consists of 2 items scored between 1 ((almost) never) to 7 ((almost) always) and subscale score ranges between 2 and 14. A higher score indicates a higher level of self-kindness, common humanity, and mindfulness, and lower scores of self-judgment, isolation, and over-identification. Total scores range from 12 to 84 (summed subscale scores), a higher score indicates a higher level of selfcompassion.
Self-Compassion Scale
Self-Compassion Scale - short form (SCS-SF). The present study will use the 12-item Dutch short-form version of the SCS-SF to measure self-compassion. The scale consists of six components, including self-kindness, self-judgment, common humanity, isolation, mindfulness and over-identification. The SCS-SF has good reliability and validity (Raes et al., 2011). In the short form, each scale consists of 2 items scored between 1 ((almost) never) to 7 ((almost) always) and subscale score ranges between 2 and 14. A higher score indicates a higher level of self-kindness, common humanity, and mindfulness, and lower scores of self-judgment, isolation, and over-identification. Total scores range from 12 to 84 (summed subscale scores), a higher score indicates a higher level of selfcompassion.
Mental Health Continuum - short form
A 14-item self-report questionnaire that assesses emotional, psychological and social well-being
Mental Health Continuum - short form
A 14-item self-report questionnaire that assesses emotional, psychological and social well-being
Inventory of Depressive Symptomatology
A clinican-administered interview assessing the severity of depressive symptoms
Inventory of Depressive Symptomatology
A clinican-administered interview assessing the severity of depressive symptoms
Inventory of Depressive Symptomatology
A clinican-administered interview assessing the severity of depressive symptoms
Inventory of Depressive Symptomatology
A clinican-administered interview assessing the severity of depressive symptoms

Full Information

First Posted
September 18, 2017
Last Updated
April 14, 2023
Sponsor
Radboud University Medical Center
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development, Pro Persona, Altrecht, Dimence, PsyQ
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1. Study Identification

Unique Protocol Identification Number
NCT03507647
Brief Title
Mindfulness Based Cognitive Therapy for Bipolar Disorder
Acronym
MBCT-BD
Official Title
Mindfulness Based Cognitive Therapy for Bipolar Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
April 23, 2018 (Actual)
Primary Completion Date
June 16, 2020 (Actual)
Study Completion Date
June 17, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Radboud University Medical Center
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development, Pro Persona, Altrecht, Dimence, PsyQ

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The current study will be a randomized controlled trial (RCT) investigating the clinical and cost-effectiveness of Mindfulness-Based Cognitive Therapy (MBCT) as an adjunct to usual care, versus usual care alone, in reducing depressive symptoms in patients with bipolar disorder. Outcome measures include depressive, (hypo)manic and anxiety symptoms, risk of relapse/recurrence, functioning and mental health/well-being. The study also aims to explore possible working mechanisms such as improvements of mindfulness and self-compassion skills. The study will have a follow-up duration of 15 months from baseline.
Detailed Description
Introduction: In the Netherlands, the lifetime prevalence of bipolar disorder (BD) is about 1.2% for men and 1.4% for women (de Graaf et al 2010). BD usually manifests itself during late adolescence or early adulthood. Its course is often chronic, with patients suffering from recurrent depressive, (hypo)manic, or mixed episodes, being symptomatic about half of the time (Judd 2002). Although hospital admissions are more common during manic episodes, illness-related disability is more strongly influenced by depressive episodes (Judd 2003). It has been estimated that about 25-50% of the patients with BD attempts suicide at least once and that the risk of suicide is about 5%(Hawton 2005). Depressive symptoms in BD are common and have been associated with negative effects on the course of bipolar disorder in terms of functional impairment and quality of life (Gutiérrez-Rojas 2008). There are limited data on how to optimize the treatment of persistent or residual depressive symptoms in BD or to improve outcomes for those patients who do not benefit sufficiently from the available treatments. In addition, there is a need for interventions that not only target symptom reduction but also help patients to cope with their illness from a wider perspective, i.e. in terms of their personal values, goals, and social roles. Mindfulness-Based Cognitive Therapy (MBCT) is an innovative intervention that has been shown effective in reducing depressive symptoms in unipolar recurrent depression (Aalderen 2012, Kuyken 2016) and appears promising for coping with severe mental illness (Davis and Kurzban 2012). Little is known about the effectiveness of MBCT for BD, with a number of pilot studies showing reductions in depressive symptoms, and one RCT showing reduction of anxiety symptoms. Considering the need for additional psychosocial treatments that not only target symptomatic but also personal recovery, these preliminary but encouraging findings warrant a larger RCT examining the efficacy of MBCT for BD in the Netherlands. Aims: As there are limited data on how to improve outcomes for those patients who do not benefit sufficiently from the available treatments, this study aims to compare MBCT to TAU as an adjunctive treatment to reduce depressive symptoms in patients with bipolar disorder. Outcomes of MBCT for BD patients will be examined both on a symptom level (depression, mania, anxiety, risk of relapse/recurrence) and in terms of functioning and mental health/well-being, including its possible working mechanisms such as improvements of mindfulness and self-compassion skills. Method: A randomized, multicenter, prospective, evaluator-blinded clinical trial of MBCT added to treatment as usual (TAU) versus TAU alone. Assessments will be conducted at baseline and at 3, 6, 9, 12 and 15 months follow-up. The intervention will consist of usual care, and for half of the participants MBCT will be offered in adjunct. MBCT is a manualised group skills-training program (Segal, Williams & Teasdale 2012) designed as a relapse prevention programme for patients with recurrent depression. The training consists of eight weekly sessions of 2.5 hours, plus one day of silent practice. The program includes both formal and informal meditation exercises. Cognitive techniques that are part of the program are education, monitoring and scheduling of activities, identification of negative automatic thoughts and devising a relapse prevention plan. The MBCT treatment will based on the 8-week MBCT course developed by Segal, Williams and Teasdale (2012), but will be adapted to address the needs of patients with a bipolar disorder. A few examples of these adaptations are: (more) psychoeducation about manic symptoms in addition to the psychoeducation about depression; introducing the 3-minute breathing space earlier in the programme and more often during sessions, especially when strong emotions are present; repeatedly bringing the focus to self-care; and making use of the mindful movement (yoga) exercises more frequently. All group sessions will be conducted at the respective mental health centres, with each group comprising 8-12 participants. MBCT courses will be taught by experienced and qualified mindfulness teachers, together with a health care professional specialised in the care for BD patients. Teacher competency will be assessed with the Mindfulness-Based Interventions - Teaching Assessment Criteria (Crane et al 2013), for which all trial sessions will be videotaped. Usual care will consist of pharmacotherapy, psycho-education and self-management interventions (usually with a psychiatric nurse).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder
Keywords
randomized controlled trial, Mindfulness based cognitive therapy, clinical effectiveness, cost-effectiveness, working mechanisms

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized, multicenter, prospective, evaluator-blinded clinical trial of MBCT added to treatment as usual (TAU) versus TAU alone
Masking
Outcomes Assessor
Masking Description
Outcomes will be assessed by independent research assistants blind to condition. Participants will be instructed to avoid unblinding as much as possible.
Allocation
Randomized
Enrollment
144 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mindfulness Based Cognitive Therapy added to usual care
Arm Type
Experimental
Arm Description
Patients in the MBCT arm will be invited to participate in MBCT added to their usual care.
Arm Title
Usual Care
Arm Type
Active Comparator
Arm Description
Usual care will typically consist of pharmacotherapy, psycho-education and self-management interventions (usually with a psychiatric nurse).
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness Based Cognitive Therapy
Other Intervention Name(s)
MBCT, Mindfulness training
Intervention Description
MBCT is a manualised group skills-training program (Segal, Williams & Teasdale 2012) consisting of eight weekly sessions of 2.5 hours, plus one day of silent practice. The program includes both formal and informal meditation exercises. Cognitive techniques that are part of the program are education, monitoring and scheduling of activities, identification of negative automatic thoughts and devising a relapse prevention plan. The MBCT treatment will be adapted to address the needs of patients with a bipolar disorder. A few examples of these adaptations are: (more) psychoeducation about manic symptoms in addition to the psychoeduction about depression; introducing the 3-minute breathing space earlier in the programme and more often during sessions, especially when strong emotions are present; repeatedly bringing the focus to self-care; and making use of the mindful movement (yoga) exercises more frequently.
Intervention Type
Other
Intervention Name(s)
Usual Care
Intervention Description
Usual care will typically consist of pharmacotherapy, psycho-education and self-management interventions (usually with a psychiatric nurse). Usual care will not be restricted, except for proscribing high-frequency psychological interventions such as (group) cognitive behavioral therapy, for practical and methodological reasons.
Primary Outcome Measure Information:
Title
Inventory of Depressive Symptomatology
Description
A clinican-administered interview assessing the severity of depressive symptoms
Time Frame
Change between baseline and 3 months
Secondary Outcome Measure Information:
Title
Structured Clinical Interview for DSM-IV-TR Disorders
Description
Diagnostic instrument to assess relapse of depressive or (hypo)manic episode
Time Frame
Change between baseline and 15 months
Title
Young Mania Rating Scale
Description
Young Mania Rating Scale (YMRS) Dutch translation. The YMRS is an 11-item clinician-administered rating scale to assess the severity of (hypo)manic symptoms. It was found to be a reliable, valid, and sensitive rating scale to measure the severity of mania (Young et al., 1978). Its total score ranges from 0 (no (hypo)manic symptoms) to 44 (severe manic symptoms).
Time Frame
Change between baseline and 3 months
Title
Young Mania Rating Scale
Description
Young Mania Rating Scale (YMRS) Dutch translation. The YMRS is an 11-item clinician-administered rating scale to assess the severity of (hypo)manic symptoms. It was found to be a reliable, valid, and sensitive rating scale to measure the severity of mania (Young et al., 1978). Its total score ranges from 0 (no (hypo)manic symptoms) to 44 (severe manic symptoms).
Time Frame
Change between baseline and 15 months
Title
Functioning Assessment Short Test
Description
Brief instrument designed to assess the main functioning problems experienced by psychiatric patients, particularly bipolar patients
Time Frame
Change between baseline and 3 months
Title
Functioning Assessment Short Test
Description
Brief instrument designed to assess the main functioning problems experienced by psychiatric patients, particularly bipolar patients
Time Frame
Change between baseline and 15 months
Title
State/Trait Anxiety Inventory
Description
self-report measure for assessing both state and trait levels of anxiety
Time Frame
Change between baseline and 3 months
Title
State/Trait Anxiety Inventory
Description
self-report measure for assessing both state and trait levels of anxiety
Time Frame
Change between baseline and 15 months
Title
Ruminative Response Scale - brooding subscale
Description
Brooding subscale of the extended version of the Ruminative Response Scale (RRS-EXT). The authors reported adequate internal consistency (α = .79) and test-retest stability (α = .62, with a one year time interval) for the brooding subscale, which consists of five items. We select the brooding subscale because over time, brooding, or rumination, has been more strongly related to levels of depression (Treynor et al., 2003). Items are scored between 1 ((almost) never) to 4 ((almost) always and subscale score ranges between 5 and 20. A higher score indicates a higher level of ruminative brooding.
Time Frame
Change between baseline and 3 months
Title
Ruminative Response Scale - brooding subscale
Description
Brooding subscale of the extended version of the Ruminative Response Scale (RRS-EXT). The authors reported adequate internal consistency (α = .79) and test-retest stability (α = .62, with a one year time interval) for the brooding subscale, which consists of five items. We select the brooding subscale because over time, brooding, or rumination, has been more strongly related to levels of depression (Treynor et al., 2003). Items are scored between 1 ((almost) never) to 4 ((almost) always and subscale score ranges between 5 and 20. A higher score indicates a higher level of ruminative brooding.
Time Frame
Change between baseline and 15 months
Title
Five Facet Mindfulness Questionnaire, short form
Description
Self-report measure consisting of 24 items divided into the subscales observing, describing, acting with awareness, non-judging and non-reactivity.
Time Frame
Change between baseline and 3 months
Title
Five Facet Mindfulness Questionnaire, short form
Description
Self-report measure consisting of 24 items divided into the subscales observing, describing, acting with awareness, non-judging and non-reactivity.
Time Frame
Change between baseline and 15 months
Title
Self-Compassion Scale
Description
Self-Compassion Scale - short form (SCS-SF). The present study will use the 12-item Dutch short-form version of the SCS-SF to measure self-compassion. The scale consists of six components, including self-kindness, self-judgment, common humanity, isolation, mindfulness and over-identification. The SCS-SF has good reliability and validity (Raes et al., 2011). In the short form, each scale consists of 2 items scored between 1 ((almost) never) to 7 ((almost) always) and subscale score ranges between 2 and 14. A higher score indicates a higher level of self-kindness, common humanity, and mindfulness, and lower scores of self-judgment, isolation, and over-identification. Total scores range from 12 to 84 (summed subscale scores), a higher score indicates a higher level of selfcompassion.
Time Frame
Change between baseline and 3 months
Title
Self-Compassion Scale
Description
Self-Compassion Scale - short form (SCS-SF). The present study will use the 12-item Dutch short-form version of the SCS-SF to measure self-compassion. The scale consists of six components, including self-kindness, self-judgment, common humanity, isolation, mindfulness and over-identification. The SCS-SF has good reliability and validity (Raes et al., 2011). In the short form, each scale consists of 2 items scored between 1 ((almost) never) to 7 ((almost) always) and subscale score ranges between 2 and 14. A higher score indicates a higher level of self-kindness, common humanity, and mindfulness, and lower scores of self-judgment, isolation, and over-identification. Total scores range from 12 to 84 (summed subscale scores), a higher score indicates a higher level of selfcompassion.
Time Frame
Change between baseline and 15 months
Title
Mental Health Continuum - short form
Description
A 14-item self-report questionnaire that assesses emotional, psychological and social well-being
Time Frame
Change between baseline and 3 months
Title
Mental Health Continuum - short form
Description
A 14-item self-report questionnaire that assesses emotional, psychological and social well-being
Time Frame
Change between baseline and 15 months
Title
Inventory of Depressive Symptomatology
Description
A clinican-administered interview assessing the severity of depressive symptoms
Time Frame
6 months
Title
Inventory of Depressive Symptomatology
Description
A clinican-administered interview assessing the severity of depressive symptoms
Time Frame
9 months
Title
Inventory of Depressive Symptomatology
Description
A clinican-administered interview assessing the severity of depressive symptoms
Time Frame
12 months
Title
Inventory of Depressive Symptomatology
Description
A clinican-administered interview assessing the severity of depressive symptoms
Time Frame
15 months
Other Pre-specified Outcome Measures:
Title
Euro-Quality of Life 5D-5L
Description
Short self-report instrument to assess quality adjusted life years
Time Frame
baseline
Title
Euro-Quality of Life 5D-5L
Description
Short self-report instrument to assess quality adjusted life years
Time Frame
3 months
Title
Euro-Quality of Life 5D-5L
Description
Short self-report instrument to assess quality adjusted life years
Time Frame
6 months
Title
Euro-Quality of Life 5D-5L
Description
Short self-report instrument to assess quality adjusted life years
Time Frame
9 months
Title
Euro-Quality of Life 5D-5L
Description
Short self-report instrument to assess quality adjusted life years
Time Frame
12 months
Title
Euro-Quality of Life 5D-5L
Description
Short self-report instrument to assess quality adjusted life years
Time Frame
15 months
Title
Trimbos/iMTA Questionnaire on Costs associated with Psychiatric illness
Description
Health service receipt interview designed for economic evaluations in the Netherlands
Time Frame
baseline
Title
Trimbos/iMTA Questionnaire on Costs associated with Psychiatric illness
Description
Health service receipt interview designed for economic evaluations in the Netherlands
Time Frame
3 months
Title
Trimbos/iMTA Questionnaire on Costs associated with Psychiatric illness
Description
Health service receipt interview designed for economic evaluations in the Netherlands
Time Frame
6 months
Title
Trimbos/iMTA Questionnaire on Costs associated with Psychiatric illness
Description
Health service receipt interview designed for economic evaluations in the Netherlands
Time Frame
9 months
Title
Trimbos/iMTA Questionnaire on Costs associated with Psychiatric illness
Description
Health service receipt interview designed for economic evaluations in the Netherlands
Time Frame
12 months
Title
Trimbos/iMTA Questionnaire on Costs associated with Psychiatric illness
Description
Health service receipt interview designed for economic evaluations in the Netherlands
Time Frame
15 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: bipolar I or II disorder having suffered at least two lifetime depressive episodes, either current or in (partial) remission at baseline (according to SCID assessment) Young Mania Rating Scale score < 8 Exclusion Criteria: a manic episode in the 3 months before the start of the trial lifetime diagnosis of schizophrenia or schizoaffective disorder, current substance abuse disorder, organic brain syndrome, antisocial or borderline personality disorder risk of suicide or aggression the presence of a concurrent significant medical condition impeding the ability to participate currently receiving regular psychological therapy previous participation in a MBCT or MBSR course
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne Speckens, Prof.
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Radboud University Nijmegen Medical Center
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6525 GC
Country
Netherlands
Facility Name
Dimence GGZ
City
Deventer
Country
Netherlands
Facility Name
Pro Persona
City
Nijmegen
Country
Netherlands
Facility Name
Altrecht GGZ
City
Utrecht
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
The authors intend to make the data available to other researchers after completion of the study and will comply with open access procedures, including open access publishing, as much as possible.
Citations:
PubMed Identifier
34735517
Citation
Hanssen I, Scheepbouwer V, Huijbers M, Regeer E, Lochmann van Bennekom M, Kupka R, Speckens A. Adverse or therapeutic? A mixed-methods study investigating adverse effects of Mindfulness-Based Cognitive Therapy in bipolar disorder. PLoS One. 2021 Nov 4;16(11):e0259167. doi: 10.1371/journal.pone.0259167. eCollection 2021.
Results Reference
derived
PubMed Identifier
33175338
Citation
Hanssen I, van der Horst N, Boele M, Lochmann van Bennekom M, Regeer E, Speckens A. The feasibility of mindfulness-based cognitive therapy for people with bipolar disorder: a qualitative study. Int J Bipolar Disord. 2020 Nov 11;8(1):33. doi: 10.1186/s40345-020-00197-y.
Results Reference
derived
PubMed Identifier
31039765
Citation
Hanssen I, Huijbers MJ, Lochmann-van Bennekom MWH, Regeer EJ, Stevens AWMM, Evers SMAA, Wensing M, Kupka RW, Speckens AEM. Study protocol of a multicenter randomized controlled trial of mindfulness-based cognitive therapy and treatment as usual in bipolar disorder. BMC Psychiatry. 2019 Apr 30;19(1):130. doi: 10.1186/s12888-019-2115-6.
Results Reference
derived

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Mindfulness Based Cognitive Therapy for Bipolar Disorder

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