Mindfulness-based cognitive therapy v. treatment as usual in people with bipolar disorder: A multicentre, randomised controlled trial.
Study Goal
The researchers aimed to investigate the added value of Mindfulness-Based Cognitive Therapy (MBCT) compared to treatment as usual (TAU) for individuals with bipolar disorder (BD) over a 15-month follow-up period.
Results Summary
MBCT + TAU was not more effective than TAU alone in reducing depressive symptoms post-treatment or at follow-up, though it improved mindfulness skills post-treatment. Participants with higher baseline depressive symptoms and functional impairment showed greater benefits from MBCT + TAU.
Population
144 participants with bipolar disorder type I and II.
Effective Dosage
Not specified
Duration
Up to 15 months follow-up
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
Mindfulness-based cognitive therapy (MBCT) + treatment as usual (TAU) | no change | current depressive symptoms | participants with bipolar disorder type I and II | 95% CI [-7.0 to 1.8], p = 0.303, d = 0.24 | was not more efficacious than TAU in reducing | #1 |
Mindfulness-based cognitive therapy (MBCT) + treatment as usual (TAU) | no change | current depressive symptoms | participants with bipolar disorder type I and II | 95% CI [-2.2 to 6.3], p = 0.037, d = 0.13 | was not more efficacious than TAU in reducing | #2 |
Mindfulness-based cognitive therapy (MBCT) + treatment as usual (TAU) | increase | mindfulness skills | participants with bipolar disorder type I and II | - | was more effective than TAU in improving | #3 |
treatment as usual (TAU) | decrease | trait anxiety | participants with bipolar disorder type I and II | - | was more effective than MBCT + TAU in reducing | #4 |
treatment as usual (TAU) | increase | mindfulness skills | participants with bipolar disorder type I and II | - | was more effective than MBCT + TAU in improving | #5 |
treatment as usual (TAU) | increase | positive mental health | participants with bipolar disorder type I and II | - | was more effective than MBCT + TAU in improving | #6 |
Mindfulness-based cognitive therapy (MBCT) + treatment as usual (TAU) | neutral | - | participants with higher depressive symptoms and functional impairment at baseline | - | benefitted more from MBCT + TAU than TAU | #7 |
BACKGROUND: Mindfulness-based cognitive therapy (MBCT) seems a promising intervention for bipolar disorder (BD), but there is a lack of randomised controlled trials (RCT) investigating this. The purpose of this multicentre, evaluator blinded RCT was to investigate the added value of MBCT to treatment as usual (TAU) in BD up to 15 months follow-up (NCT03507647). METHODS: A total of 144 participants with BD type I and II were randomised to MBCT + TAU (n = 72) and TAU (n = 72). Primary outcome was current depressive symptoms. Secondary outcomes were current (hypo)manic and anxiety symptoms, recurrence rates, rumination, dampening of positive affect, functional impairment, mindfulness skills, self-compassion, and positive mental health. Potential moderators of treatment outcome were examined. RESULTS: MBCT + TAU was not more efficacious than TAU in reducing current depressive symptoms at post-treatment (95% CI [-7.0 to 1.8], p = 0.303, d = 0.24) or follow-up (95% CI [-2.2 to 6.3], p = 0.037, d = 0.13). At post-treatment, MBCT + TAU was more effective than TAU in improving mindfulness skills. At follow-up, TAU was more effective than MBCT + TAU in reducing trait anxiety and improving mindfulness skills and positive mental health. Exploratory analysis revealed that participants with higher depressive symptoms and functional impairment at baseline benefitted more from MBCT + TAU than TAU. CONCLUSIONS: In these participants with highly recurrent BD, MBCT may be a treatment option in addition to TAU for those who suffer from moderate to severe levels of depression and functional impairment. TRIAL REGISTRATION: ClinicalTrials.gov, NCT03507647. Registered the 25 April 2018, https://www.clinicaltrials.gov/ct2/show/NCT01126827.