Bipolar Disorder Clinical Trial
Official title:
Group Dialectical Behavioural Therapy for Mood Instability Within Bipolar Disorder: An Open Trial
NCT number | NCT02637401 |
Other study ID # | 1415/002 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | March 2015 |
Est. completion date | June 2016 |
Verified date | May 2018 |
Source | University of Exeter |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Bipolar Disorders (BD) typically involve repeated episodes of both depression and excessively
high mood or irritability (hypomania or mania). BD presents considerable challenges for the
individual, his or her supporters, and society more generally. Medication is generally
considered to be the mainstay treatment, however a substantial number of individuals with BD
continue to experience episodes despite use of medication. Furthermore, ongoing mood
instability either outside of episodes, or as the main feature of their BD, is a significant
difficulty experienced by many. Whilst studies suggest that certain psychological therapies
can be helpful for people experiencing full bipolar episodes, or to reduce risk of future
episodes, there are no evidencebased psychological therapies available for individuals
experiencing ongoing mood instability. Dialectical Behaviour Therapy (DBT) was developed
several decades ago as an approach for people with Borderline Personality Disorder. DBT aims
to give individuals who experience rapid and intense shifts in affect skills for managing
this. Despite the many similarities in the symptoms experienced by individuals with
Borderline Personality Disorder and those with Bipolar Disorder only a small number of
studies have tested DBT for BD, and no studies to date have specifically investigated DBT as
a means to help individuals with ongoing mood instability. We have developed a version of
groupbased DBT that draws upon our own research to adapt standard DBT for this client group
(DBTBD).
The group is designed to be delivered efficiently within the U.K. healthcare system whilst
meeting the needs of individual participants through use of additional individual sessions
and a mobile phone application. The current study investigates how acceptable DBTBD is to
clinicians and patients, and whether - for the small number of individuals in the study
-changes in symptoms and key ways of thinking and behaving appear to take place across the
period of treatment.
Status | Completed |
Enrollment | 13 |
Est. completion date | June 2016 |
Est. primary completion date | January 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion criteria for patient participants are: i) aged 18 or over; i) meets DSMV criteria
for Bipolar Spectrum Disorder; iii) current bipolar mood instability (over the past two
years numerous periods with hypomanic symptoms that do not meet criteria for a hypomanic
episode and numerous periods with depressive symptoms that do not meet criteria for a
depressive episode, continuing into the past month); iv) client wishes to engage in
psychological therapy that focusses primarily on ongoing mood instability and its
consequences. Exclusion criteria are: i) current substance dependence disorder; ii) currently receiving other psychological therapy; iii) the patient is currently actively suicidal; iv) presenting difficulties that are characteristic of Borderline Personality Disorder rather than Bipolar Disorder and that would be an early treatment target in standard DBT (frequent and serious deliberate selfharm, marked disturbance in ability to form or maintain interpersonal relationships); v) presence of another area of difficulty that the therapist and client believe should be the primary focus of intervention (for example panic disorder with agoraphobia, Post Traumatic Stress Disorder); vi) the information available suggests that the person may present a significant risk to other group members (such as aggression, likelihood of carrying out sexual or other exploitation); vii) the person lacks capacity to consent to treatment or research participation; viii) currently experiencing an episode of mania. |
Country | Name | City | State |
---|---|---|---|
United Kingdom | University of Exeter | Exeter | Devon |
Lead Sponsor | Collaborator |
---|---|
University of Exeter |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Acceptability of the therapy (% completing treatment) | 10 months | ||
Primary | Acceptability of the therapy and study procedures | Qualitiative feedback from participants | 10 months | |
Primary | Feasibility of the study procedures | recruitment rate; feedback from referrers and clincians / researchers | 10 months | |
Secondary | Clinical effectiveness | symptoms, quality of life, recovery status. Analysis focuses upon the sensitvity of these measures to change, and pre-post correlations. | 15 months | |
Secondary | Process measures | self report measures of key psychological processes hypothesised to be changed by therapy. Analysis focuses upon the sensitvity of these measures to change, and pre-post correlations. | 10 months |
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