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Psychosocial treatment and interventions for bipolar disorder: a systematic review



Bipolar disorder (BD) is a chronic disorder with a high relapse rate, significant general disability and burden and with a psychosocial impairment that often persists despite pharmacotherapy. This indicates the need for effective and affordable adjunctive psychosocial interventions, tailored to the individual patient. Several psychotherapeutic techniques have tried to fill this gap, but which intervention is suitable for each patient remains unknown and it depends on the phase of the illness.


The papers were located with searches in PubMed/MEDLINE through May 1st 2015 with a combination of key words. The review followed the recommendations of the Preferred Items for Reporting of Systematic Reviews and Meta-Analyses statement.


The search returned 7,332 papers; after the deletion of duplicates, 6,124 remained and eventually 78 were included for the analysis. The literature supports the usefulness only of psychoeducation for the relapse prevention of mood episodes and only in a selected subgroup of patients at an early stage of the disease who have very good, if not complete remission, of the acute episode. Cognitive-behavioural therapy and interpersonal and social rhythms therapy could have some beneficial effect during the acute phase, but more data are needed. Mindfulness interventions could only decrease anxiety, while interventions to improve neurocognition seem to be rather ineffective. Family intervention seems to have benefits mainly for caregivers, but it is uncertain whether they have an effect on patient outcomes.


The current review suggests that the literature supports the usefulness only of specific psychosocial interventions targeting specific aspects of BD in selected subgroups of patients.


Our contemporary understanding of bipolar disorder (BD) suggests that there is an unfavorable outcome in a significant proportion of patients [1, 2]. In spite of recent advances in pharmacological treatment, many BD patients will eventually develop chronicity with significant general disability and burden. The burden will be significant also for their families and the society as a whole [3, 4]. Today, we also know that unfortunately, symptomatic remission is not identical and does not imply functional recovery [57].

Since pharmacological treatment often fails to address all the patients’ needs, there is a growing need for the development and implementation of effective and affordable interventions, tailored to the individual patient [8]. The early successful treatment, with full recovery if possible, as well as the management of subsyndromal symptoms and of psychosocial stress and poor adherence are factors predicting earlier relapse and poor overall outcome [9, 10].

In this frame, there are several specific adjunctive psychotherapies which have been developed with the aim of filling the above gaps and eventually improve the illness outcome [11], but it is still unclear whether they truly work and which patients are eligible and when [1219].

The current study is a systematic review of the efficacy of available psychosocial interventions for the treatment of adult patients with BD.


Reports investigating psychotherapy and psychosocial interventions in BD patient samples were located with searches in Pubmed/MEDLINE through May 1, 2015. Only reports in English language were included.

The Pubmed database was searched using the search terms ‘bipolar’ and ‘psychotherapy’ or ‘cognitive-behavioral’ or ‘CBT’ or ‘psychoeducation’ or ‘interpersonal and social rhythm therapy’ or ‘IPSRT’ or ‘family intervention’ or ‘family therapy’ or ‘group therapy’ or ‘intensive psychosocial intervention’ or ‘cognitive remediation’ or ‘functional remediation’ or ‘Mindfulness’.

The following rules were applied for the selection of papers:

  1. 1.

    Papers in English language.

  2. 2.

    Randomized controlled trials.

This review followed the recommendations of the Preferred Items for Reporting of Systematic Reviews and Meta-Analyses (PRISMA) statement [20].


The search returned 7,332 papers, and after the deletion of duplicates 6,124 remained for further assessment. After assessing these papers on the basis of title and abstract, the remaining papers were (Figure 1). The number of paper reported for each intervention includes RCTs, post hoc analyses and meta-analyses together.

Figure 1

The PRISMA flowchart.

Cognitive-behavioural therapy (CBT)

The efficacy of CBT in BD was investigated in 14 studies which utilized CBT as adjunct treatment to pharmacotherapy or treatment as usual (TAU). They utilized some kind of control intervention which should not be considered as an adequate placebo. It is also interesting that the oldest study was conducted in 2003.

This first study lasted 12 months and concerned 103 BD-I patients during the acute depressive phase and randomized them to 14 sessions of CBT or a control intervention. There was not any placebo condition. These authors reported that at end point fewer patients in the CBT group relapsed in comparison to controls (44 vs. 75%; HR = 0.40, P = 0.004), had shorter episode duration, less admissions and mood symptoms, and higher social functioning [21]. It was disappointing that the extension of this study (18 months follow-up) was negative concerning the relapse rate [22].

A second trial included 52 BD patients and was also negative concerning the long-term efficacy after comparing CBT plus additional emotive techniques vs. TAU [23]. On the other hand, the comparison of CBT plus psychoeducation vs. TAU in 40 BD patients reported a beneficial effect even after 5 years in terms of symptoms and social–occupational functioning. However, that study did not report the rate of recurrences and the time to recurrence [24]. A study in 79 BD patients (52 BD-I and 27 BD-II) compared CBT plus psychoeducation vs. psychoeducation alone and reported that the combined treatment group had 50% fewer depressed days per month, while at the same time the psychoeducation alone group had more antidepressant use [25]. Another study on 41 BD patients randomized to CBT vs. TAU reported similar results and an improvement in symptoms, frequency and duration of episodes [26].

An 18-month study compared CBT vs. TAU in 253 BD patients and reported that at end point, there were no differences between groups with more than half of the patients having a recurrence. It is interesting that a post hoc analysis suggested that CBT was significantly more effective than TAU in those patients with fewer than 12 previous episodes, but less effective in those with more episodes [13]. Similar negative results were reported concerning the number of episodes and time to relapse by another 12-month study of CBT vs. TAU in 50 BD patients in remission [17]. Again, negative findings concerning the relapse rate were reported by a 2-year study on 76 BD patients randomized to receive 20 sessions of CBT vs. support therapy [15]. Finally, the use of combined CBT and pharmacotherapy in 40 patients with refractory bipolar disorder suggested that the combination group had less hospitalization events in comparison to the group in the 12-month evaluation (P = 0.015) and lower depression and anxiety in the 6-month (P = 0.006; P = 0.019), 12-month (P = 0.001; P < 0.001) and 5-year (P < 0.001, P < 0.001) evaluation time points. However it is interesting that after the 5-year follow-up, 88.9% of patients in the control group and 20% of patients in the combination group showed persistent affective symptoms and difficulties in social–occupational functioning [27].

The use of CBT in BD comorbid with social anxiety disorder is of doubtful efficacy [28], while there are some preliminary data on the efficacy of an Internet-based CBT intervention [29] as well as recovery-focused add-on CBT [30] and CBT for insomnia [31] in comparison to TAU.

The review of the available data so far give limited support for the usefulness of CBT during the acute phase of bipolar depression as adjunctive treatment in patients with BD, but definitely not for the maintenance phase. During the maintenance phase, booster sessions might be necessary, but the data are generally overall negative. Probably, patients at earlier stages of the illness might benefit more from CBT. Unfortunately the type of patients who are more likely to benefit from CBT constitutes a minority in usual clinical practice.


The basic concept behind psychoeducation for BD concerns the training of patients regarding the overall awareness of the disorder, treatment adherence, avoiding of substance abuse and early detection of new episodes. The efficacy of psychoeducation in BD was investigated in 30 studies, all of which utilized psychoeducation as adjunct treatment to pharmacotherapy or TAU. All these studies utilize some kind of control intervention which should not be considered as an adequate placebo. It is also interesting that the oldest study was conducted in 1991.

The earliest psychoeducational study was open and uncontrolled and reported that giving information about lithium improved the overall attitude towards treatment [32, 33]. A similar small study was conducted a few years later and reported similar results [34]. However, the first study on the wide teaching of patients to recognize and identify the components of their disease with emphasis on early symptoms of relapse and recurrence and to seek professional help as early as possible had not been conducted until 1999. It included 69 patients for 18 months and compared psychoeducation (limited number of sessions; 7–12) vs. TAU. It reported a significant prolongation of the time to first manic relapse (P = 0.008) and significant reductions in the number of manic relapses over 18 months (30 vs. 52%; P = 0.013) as well as improved overall social functioning. Psychoeducation had no effect on depressive relapses [35].

In a more systematic way, the efficacy of the adjunctive group psychoeducation was tested by the Barcelona group. Their trial included 120 euthymic BD patients who were randomly assigned to 21 sessions of group psychoeducation vs. non-specific group meetings. The study included a follow-up with a duration of 2 and 5 years. The results suggested that psychoeducation exerted a beneficial effect on the rate of and the time to recurrence as well as concerning hospitalizations per patient. At the end of the 2-year follow-up, 23 subjects (92%) in the control group fulfilled the criteria for recurrence versus 15 patients (60%) in the psychoeducation group (P < 0.01). This beneficial effect was high and was not reduced after 5 years (any episode 0.79 vs. 0.87; mania 0.40 vs. 0.57; hypomania 0.27 vs. 0.42 and mixed episodes 0.34 vs. 0.61), except for depressive episodes (0.91 vs. 0.80) [3638].

The literature suggests that psychoeducation should be broad and that enhanced relapse prevention alone does not seem to work. This was the conclusion from another study with a different design. That study reported that only occupational functioning, but not time to recurrence, improved with an intervention consisting of training community mental health teams to deliver enhanced relapse prevention [39]. Additionally, a study with a 12-month follow-up and with a similar design to the first study of the Barcelona group, but with 16 sessions, reported no differences between groups in mood symptoms, psychosocial functioning and quality of life. It did find, however, that there was a difference in the subjectively perceived overall clinical improvement by subjects who received psychoeducation. The authors suggested that characteristics of the sample could explain this discrepancy, as patients with a more advanced stage of disease might have a worse response to psychoeducation [16]. In accordance with the above, a post hoc analysis of the original Barcelona data revealed that patients with more than seven episodes did not show significant improvement with group psychoeducation in time to recurrence, and those with more than 14 episodes did not benefit from the treatment in terms of time spent ill [40]. A 2-year follow-up in 108 BD patients investigated psychoeducation plus pharmacotherapy vs. pharmacotherapy alone. Psychoeducation concerned eight, 50-min sessions of psychological education, followed by monthly telephone follow-up care and psychological support. The results suggested that psychoeducation improved medication compliance (P = 0.008) and quality of life (P < 0.001) and had fewer hospitalizations (P < 0.001) [41]. Another study randomized 80 BD patients to either the psychoeducation or the control group and reported that the psychoeducation group scored significantly higher on functioning levels (emotional functioning, intellectual functioning, feelings of stigmatization, social withdrawal, household relations, relations with friends, participating in social activities, daily activities and recreational activities, taking initiative and self-sufficiency, and occupation) (P < 0.05) compared with the control group after psychoeducation [42].

A prospective 5-year follow-up of 120 BD patients suggested that group psychoeducation might be more cost-effective [43]. In support of the cost-effectiveness of psychoeducation was one trial in 204 BD patients which compared 20 sessions of CBT vs. 6 sessions of group psychoeducation and reported that overall the outcome was similar in the two groups in terms of reduction of symptoms and likelihood of relapse, but psychoeducation was associated with a decrease of costs ($180 per subject vs. $1,200 per subject for CBT) [44] Currently, there are some proposals of online psychoeducation programmes, but results are still inconclusive or pending [45, 46].

More complex multimodal approaches and multicomponent care packages have been developed and usually psychoeducation is a core element. One of these packages also included CBT and elements of dialectical behaviour therapy and social rhythms and has shown a beneficial effect after the 1-year follow-up in comparison to TAU [47]. Another included a combination of CBT plus psychoeducation and reported that it was more effective in comparison to TAU in 40 refractory BD patients concerning hospitalization and residual symptoms at 12 months follow-up [27]. A collaborative care study on 138 patients and follow-up of 12 months also gave positive results [48]. One multicentred Italian study assessed the efficacy of the Falloon model of psychoeducational family intervention (PFI), originally developed for schizophrenia management and adapted to BD-I disorder. It included 137 recruited families, of which 70 were allocated to the experimental group and 67 to the TAU group. At the end of the intervention, significant improvements in patients’ social functioning and relatives’ burden were found in the treated group compared to TAU [49]. In general, the beneficial effect seems to be present concerning manic but not depressive episodes [50, 51], while a benefit on social role function and quality of life seems also to be present [50].

The comparison of 12 sessions of psychoeducation vs. TAU in 71 BD patients reported that at 6 weeks, the intervention improved treatment adherence [52], while another on 61 BD-II patients reported no significant effect on the regulation of biological rhythms when compared to standard pharmacological treatment [53]. No significant effect was reported concerning the quality of life by another recent study on 61 young bipolar adults [54]. On the contrary, a trial on 47 BD patients reported that a psychoeducation programme designed for internalized stigmatization may have positive effects on the internalized stigmatization levels of patients with bipolar disorder [55].

There is preliminary evidence that a Web-based treatment approach in BD (‘Living with Bipolar’—LWB intervention) is feasible and potentially effective [56]; however, other Web-based attempts returned negative results [57]. Automated mobile-phone intervention is another option and it has been reported to be feasible, acceptable and might enhance the impact of brief psychoeducation on depressive symptoms in BD. However, sustainment of gains from symptom self-management mobile interventions, once stopped, may be limited [58].

One meta-analysis of 16 studies, 8 of which provided data on relapse reported that psychoeducation appeared to be effective in preventing any relapse (OR: 1.98–2.75; NNT: 5–7) and manic/hypomanic relapse (OR: 1.68–2.52; NNT: 6–8), but not depressive relapse. That meta-analysis reported that group, but not individually, delivered interventions were effective against both poles of relapse [59].

In summary, the literature suggests that interventions of 6-month group psychoeducation seem to exert a long-lasting prophylactic effect. However this is rather restricted to manic episodes and to patients at the earlier stages of the disease who have achieved remission before the intervention has started. Although the mechanism of action of psychoeducation remains unknown, it is highly likely that the beneficial effect is mediated by the enhancement of treatment adherence, the promoting of lifestyle regularity and healthy habits and the teaching of early detection of prodromal signs.

Interpersonal and social rhythm therapy (IPSRT)

Interpersonal and social rhythm therapy is based on the hypothesis that in vulnerable individuals, the experience of stressful life events and unstable or disrupted daily routines can lead to affective episodes via circadian rhythm instability [18]. In this frame, IPSRT includes the management of affective symptoms through improvement of adherence to medication and stabilizing social rhythms and the resolution of interpersonal problems. Four papers investigating its efficacy were identified.

The first study concerning its efficacy in BD included 175 acutely ill BD patients and followed them for 2 years. It included four treatment groups, reflecting IPSRT vs. intensive clinical management during the acute and the maintenance phase. The results revealed no difference between interventions in terms of time to remission and in the proportion of patients achieving remission (70 vs. 72%), although those patients who received IPSRT during the acute treatment phase survived longer without an episode and showed higher regularity of social rhythms [60]. In spite of some encouraging findings from post hoc analysis, there were eventually no significant differences between genders and concerning the improvement in occupational functioning [61]. More recently, a 12-week study in which unmedicated depressed BD-II patients were randomized to IPSRT (N = 14) vs. treatment with quetiapine (up to 300 mg/day; N = 11), showed that both groups experienced significant reduction in symptoms over time, but there were no group-by-time interactions. Response and drop-out rates were similar [62]. Finally, one 78-week trial investigated the efficacy of IPSRT vs. specialist supportive care on depressive and mania outcomes and social functioning, and mania outcomes in 100 young BD patients. The results revealed no significant difference between therapies [63].

Overall, there are no convincing data on the usefulness of IPSRT during the maintenance phase of BD. There are, however, some data suggesting that if applied early and particularly already during the acute phase, it might prolong the time to relapse.

Family intervention

The standard family intervention for BD targets the whole family and not only the patient and includes elements of psychoeducation, communication enhancement and problem-solving skills training. It also includes support and self-care training for caregivers. Fifteen papers concerning the efficacy of family intervention in BD were found.

The first study on this intervention took part in 1991 and reported that carer-focused interventions improve the knowledge of the illness [64]. Since then, there have been a number of studies which in general support the use of adjunctive family-focused treatment. There are different designs and approaches which were tested in essentially open trials.

One intervention design consists of 21 1-h sessions which combine psychoeducation, communication skills training and problem-solving training. The sessions take place at home and included both the patient and his/her family during the post-episode period. The treatment has shown its efficacy vs. crisis management in 101 BD patients in reducing relapses (35 vs. 54%) and increasing time to relapse (53 vs. 73 weeks, respectively) [65, 66]. It was also reported to reduce hospitalization risk compared with individual treatment (12 vs. 60%) [67]. It is important that the benefits extended to the 2-year follow-up were particularly useful for depressive symptoms, in families with high expressed emotion and for the improvement of medication adherence [66]. Similar results were reported by a study of 81 BD patients and 33 family dyads, which reported that the odds ratio for hospitalization at 1-year follow-up was related with high perceived criticism (by the patients from their relatives), poor adherence and with the relatives’ lack of knowledge concerning BD (OR: 3.3; 95% CI 1.3–8.6) [68].

Adjunctive psychoeducational marital intervention in acutely ill patients was reported to have a beneficial effect concerning medication adherence and global functioning, but not for symptoms [69]. Neither adjunctive family therapy nor adjunctive multifamily group therapy improves the recovery rate from acute bipolar episodes when compared with pharmacotherapy alone [14]. These interventions could be beneficial for patients from families with high levels of impairment and could result in a reduction of both the number of depressive episodes and the time spent in depression (Cohen d = 0.7–1.0) [70]. In this frame, in those patients who recovered from the intake episode, multifamily group therapy was associated with the lowest hospitalization risk [71].

Another format included a 90-min duration, delivered to caregivers of euthymic BD patients; after 15-months, it was reported to have both reduced the risk of recurrence in comparison to a control group (42 vs. 66%; NNT: 4.1 with 95% CI 2.4–19.1) and also to have delayed recurrence [72]. It was particularly efficacious in the prevention of hypomanic/manic episodes and also in the reduction of the overall family burden [73]. It had been shown before that carer-focused interventions improve the knowledge of the illness [64], reduce burden [74] and also reduce the general and mental health risk of caregivers [75].

Another format of intervention included 12 sessions of group psychoeducation for the patients and their families. It has been found superior to TAU in 58 BD patients concerning the prevention of relapses, the decrease of manic symptoms and the improvement of medication adherence [76]. Finally, the comparison of family-based therapy (FBT) vs. brief psychoeducation (crisis management) in 108 patients with BD reported that the outcome depended on the existing levels of appropriate self-sacrifice [77].

Overall, the literature supports the conclusion that interventions which focus on families and caregivers exert a beneficial impact on family members, but the effect on the patients themselves is controversial. The effect includes issues ranging from subjective well-being to general health, but it is almost certain that there is a beneficial effect on issues like treatment adherence.

Intensive psychosocial intervention

There are three papers investigating various methods of intensive psychosocial intervention. ‘Intensive’ psychotherapy has been tested on 293 acutely depressive BD outpatients in a multi-site study. Patients were randomized to 3 sessions of psychoeducation vs. up to 30 sessions of intensive psychotherapy (family-focused therapy, IPSRT or CBT). The results suggested that the intensive psychotherapy group showed higher recovery rates, shorter times to recovery and greater likelihood of being clinically well in comparison to patients on short intervention [78]. The functional outcome was also reported to be better after 1 year [79]. A second trial randomized 138 BD patients to receive collaborative care (contracting, psychoeducation, problem-solving treatment, systematic relapse prevention and monitoring of outcomes) vs. TAU. The results suggested that collaborative care had a significant and clinically relevant effect on the number of months with depressive symptoms, as well as on severity of depressive symptoms, but there was no effect on symptoms of mania or on treatment adherence [48].

Cognitive remediation (CR) and functional remediation (FR)

Cognitive remediation and functional remediation tailored to the needs of BD patients include education on neurocognitive deficits, communication, autonomy and stress management. There are five papers on the efficacy of CR and FR.

One uncontrolled study in 15 BD patients applied a type of CR and focused on mood monitoring and residual depressive symptoms, organization, planning and time management, attention and memory. The results suggested that there was an improvement of residual depressive symptoms, executive functions and general functioning. Patients with greater neurocognitive impairment had less benefit from the intervention [80]. The combination of neurocognitive techniques with psychoeducation and problem solving within an ecological framework was tested in a multicentre trial in 239 euthymic BD patients with a moderate–severe degree of functional impairment (N = 77) vs. psychoeducation (N = 82) and vs. TAU (N = 80). At end point, the combined programme was superior to TAU, but not to psychoeducation alone [81, 82]. Finally, a small study in 37 BD and schizoaffective patients tested social cognition and interaction training (SCIT) as adjunctive to TAU (N = 21) vs. TAU alone (N = 16). There was no difference between groups concerning social functioning, but there was a superiority of the combination group in the improvement of emotion perception, theory of mind, hostile attribution bias and depressive symptoms [83]. A post hoc analysis using data of 53 BD-II outpatients compared FR vs. psychoeducation and vs. TAU, but the results were negative [84].

Mindfulness-based interventions

Mindfulness-based intervention aims to enhance the ability to keep one’s attention on purpose in the present moment and non-judgmentally. Specifically for BD patients, it includes education about the illness and relapse-prevention, combination of cognitive therapy and training in mindfulness meditation to increase the awareness of the patterns of thoughts, feelings and bodily sensations and the development of a different way (non-judgementally) of relating to thoughts, feelings and bodily sensations. It also promotes the ability of the patients to choose the most skilful response to thoughts, feelings or situations. There are eight studies on the efficacy of mindfulness-based intervention in BD.

The first study concerning the application of mindfulness-based cognitive therapy (MBCT) in BD tested it vs. waiting list and included only eight patients in each group. The results suggested a beneficial effect with a reduction in anxiety and depressive symptoms [85]. A second study included 23 BD patients and 10 healthy controls and investigated MBCT vs. waiting list and the results were compared with those of 10 healthy controls. The results suggested that following MBCT, there were significant improvements in BD patients concerning mindfulness, anxiety and emotion regulation, working memory, spatial memory and verbal fluency compared to the waiting list group [86]. The biggest study so far concerning MBCT included 95 BD patients and tested MBCT as adjunctive to TAU (N = 48) vs. TAU alone (N = 47) and followed the patients for 12 months. The results showed no difference between treatment groups in terms of relapse and recurrent rates of any mood episodes. There was some beneficial effect of MBCT on anxiety symptoms [87, 88]. Recently, the focus has expanded to analyze the impact of MBCT on brain activity and cognitive functioning in BD, but the findings are difficult to interpret [86, 89, 90].

A study which applied dialectical behaviour therapy in which mindfulness represented a large component also reported some positive outcomes [91]. One study on mindfulness training reported negative results in BD patients [92].

In conclusion, the literature does not support a beneficial effect of MBCT on the core issues of BD. There are some data suggesting a beneficial effect on anxiety in BD patients. So far, there are no data supporting its efficacy in the prevention of recurrences.


The current review suggests that the literature supports the usefulness only of psychoeducation for the relapse prevention of mood episodes and unfortunately only in a selected subgroup of patients at an early stage of the disease who have very good if not complete remission of the acute episode. On the other hand, CBT and IPSRT could have some beneficial effect during the acute phase, but more data are needed. Mindfulness interventions could only decrease anxiety, while interventions to improve neurocognition seem to be rather ineffective. Family intervention seems to have benefits mainly for caregivers, but it is uncertain whether they have an effect on patient outcomes. A summary of the specific areas of efficacy for each of the above-mentioned interventions is shown in Table 1.

Table 1 Specific psychosocial interventions and their targeted therapeutic effect in BD

An additional important conclusion is that concerning the quality of the data available: the studies on BD patients suffer from the same limitations and methodological problems as all psychotherapy trials do. It is well known that this kind of studies suffers from problems pertaining to blindness and the nature of the control intervention. Additionally, the training of the therapist and the setting itself might play an important role. It is quite different to apply the same intervention in specialized centres than in real-world settings in everyday clinical practice. Even worse, research is not done in a standardized way and the gathering of data is far from systematic. The studies are rarely registered, adverse events are not routinely assessed, outcomes are not hierarchically stated a priori and too many post hoc analyses have been published without being stated as such. There is a lack of replication of the same treatment by different research groups under the same conditions.

There are different theories on the mechanisms responsible for the efficacy of the psychosocial treatments. One suggestion concerns the enhancement of treatment adherence [93], while another proposes that improving lifestyle and especially biological rhythms, food intake and social zeitgebers could be the key factors [60]. Also, it has been proposed that the mechanism concerns the changing of dysfunctional attitudes [23], the improvement of family interactions [94] or the enhanced ability for the early identification of signs of relapse [35].

Overall, it seems that psychosocial interventions are more efficacious when applied on patients who are at an early stage of the disease and who were euthymic when recruited [14, 95]. According to these post hoc analyses, a higher number of previous episodes [13, 40] as well as a higher psychiatric morbidity and more severe functional impairment [96] might reduce treatment response, although the data are not conclusive [97]. Also, a differential effect has been proposed with neuroprotective strategies being better during the early stages [98] and rehabilitative interventions being preferable at later stages [99].

It is unclear whether IPSRT and CBT are efficacious during the acute episodes, but there are some data in support [13, 60, 78]. Maybe specific family environment characteristics might influence the response to treatment [70, 100]. Probably, there were subpopulations who especially benefited from these treatments [13, 70], but these assumptions are based on post hoc analyses alone.

It should be mentioned that most of the research concerns pure and classic BD-I patients, although there are some rare data concerning special populations such as BD-II [36, 62], schizoaffective disorder [101, 102], patients with high suicide risk [85, 103, 104] and patients with comorbid substance abuse [105, 106].

It is interesting to note that the literature suggests that the benefits of psychosocial interventions if achieved could last for up to 5 years [36, 107], although some patients might need booster sessions [23, 108]. The complete range of the effect these interventions have is still uncharted. Although it is reasonable to expect a beneficial effect in a number of problems, including suicidality, research data on these issues are virtually non-existent [103, 104].


In conclusion, the literature supports the notion that adjunctive specific psychological treatments can improve specific illness outcomes. Although the data are rare, it seems reasonable that any such intervention should be applied as early as possible and should always be tailored to the specific needs of the patient in the context of personalized patient care, since it is accepted that both the patients and their relatives have different needs and problems depending on the stage of the illness.


  1. 1.

    Fountoulakis KN, Kasper S, Andreassen O, Blier P, Okasha A, Severus E et al (2012) Efficacy of pharmacotherapy in bipolar disorder: a report by the WPA section on pharmacopsychiatry. Eur Arch Psychiatry Clin Neurosci 262(Suppl 1):1–48

    PubMed  Google Scholar 

  2. 2.

    Grunze H, Vieta E, Goodwin GM, Bowden C, Licht RW, Moller HJ et al (2013) The World Federation of Societies of Biological Psychiatry (WFSBP) guidelines for the biological treatment of bipolar disorders: update 2012 on the long-term treatment of bipolar disorder. World J Biol Psychiatry 14(3):154–219

    PubMed  Google Scholar 

  3. 3.

    Murray CJ, Vos T, Lozano R, Naghavi M, Flaxman AD, Michaud C et al (2012) Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet 380(9859):2197–2223

    PubMed  Google Scholar 

  4. 4.

    Rosa AR, Reinares M, Michalak EE, Bonnin CM, Sole B, Franco C et al (2010) Functional impairment and disability across mood states in bipolar disorder. Value Health 13(8):984–988

    PubMed  Google Scholar 

  5. 5.

    Tohen M, Hennen J, Zarate CM Jr, Baldessarini RJ, Strakowski SM, Stoll AL et al (2000) Two-year syndromal and functional recovery in 219 cases of first-episode major affective disorder with psychotic features. Am J Psychiatry 157(2):220–228

    CAS  PubMed  Google Scholar 

  6. 6.

    Rosa AR, Reinares M, Amann B, Popovic D, Franco C, Comes M et al (2011) Six-month functional outcome of a bipolar disorder cohort in the context of a specialized-care program. Bipolar Disord 13(7–8):679–686

    PubMed  Google Scholar 

  7. 7.

    Reinares M, Papachristou E, Harvey P, Mar BC, Sanchez-Moreno J, Torrent C et al (2013) Towards a clinical staging for bipolar disorder: defining patient subtypes based on functional outcome. J Affect Disord 144(1–2):65–71

    PubMed  Google Scholar 

  8. 8.

    Catala-Lopez F, Genova-Maleras R, Vieta E, Tabares-Seisdedos R (2013) The increasing burden of mental and neurological disorders. Eur Neuropsychopharmacol 23(11):1337–1339

    CAS  PubMed  Google Scholar 

  9. 9.

    De DC, Ezquiaga E, Agud JL, Vieta E, Soler B, Garcia-Lopez A (2012) Subthreshold symptoms and time to relapse/recurrence in a community cohort of bipolar disorder outpatients. J Affect Disord 143(1–3):160–165

    Google Scholar 

  10. 10.

    Berk L, Hallam KT, Colom F, Vieta E, Hasty M, Macneil C et al (2010) Enhancing medication adherence in patients with bipolar disorder. Hum Psychopharmacol 25(1):1–16

    PubMed  Google Scholar 

  11. 11.

    Fountoulakis K (2015) Bipolar disorder: an evidence-based guide to manic depression. Springer, New York

    Google Scholar 

  12. 12.

    Geddes JR, Miklowitz DJ (2013) Treatment of bipolar disorder. Lancet 381(9878):1672–1682

    CAS  PubMed  Google Scholar 

  13. 13.

    Scott J, Paykel E, Morriss R, Bentall R, Kinderman P, Johnson T et al (2006) Cognitive-behavioural therapy for severe and recurrent bipolar disorders: randomised controlled trial. Br J Psychiatry 188:313–320

    PubMed  Google Scholar 

  14. 14.

    Miller IW, Solomon DA, Ryan CE, Keitner GI (2004) Does adjunctive family therapy enhance recovery from bipolar I mood episodes? J Affect Disord 82(3):431–436

    PubMed  Google Scholar 

  15. 15.

    Meyer TD, Hautzinger M (2012) Cognitive behaviour therapy and supportive therapy for bipolar disorders: relapse rates for treatment period and 2-year follow-up. Psychol Med 42(7):1429–1439

    CAS  PubMed  Google Scholar 

  16. 16.

    de Barros PK, de O Costa L, Silval KI, Dias VV, Roso MC, Bandeira M et al (2013) Efficacy of psychoeducation on symptomatic and functional recovery in bipolar disorder. Acta Psychiatr Scand 127(2):153–158

    Google Scholar 

  17. 17.

    Gomes BC, Abreu LN, Brietzke E, Caetano SC, Kleinman A, Nery FG et al (2011) A randomized controlled trial of cognitive behavioral group therapy for bipolar disorder. Psychother Psychosom 80(3):144–150

    CAS  PubMed  Google Scholar 

  18. 18.

    Reinares M, Sanchez-Moreno J, Fountoulakis KN (2014) Psychosocial interventions in bipolar disorder: what, for whom, and when. J Affect Disord 156:46–55

    PubMed  Google Scholar 

  19. 19.

    Fountoulakis KN, Siamouli M (2009) Re: how well do psychosocial interventions work in bipolar disorder? Can J Psychiatry (Revue canadienne de psychiatrie) 54(8):578

    Google Scholar 

  20. 20.

    Moher D, Liberati A, Tetzlaff J, Altman DG (2010) Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Int J Surg 8(5):336–341

    PubMed  Google Scholar 

  21. 21.

    Lam DH, Watkins ER, Hayward P, Bright J, Wright K, Kerr N et al (2003) A randomized controlled study of cognitive therapy for relapse prevention for bipolar affective disorder: outcome of the first year. Arch Gen Psychiatry 60(2):145–152

    PubMed  Google Scholar 

  22. 22.

    Lam DH, McCrone P, Wright K, Kerr N (2005) Cost-effectiveness of relapse-prevention cognitive therapy for bipolar disorder: 30-month study. Br J Psychiatry 186:500–506

    PubMed  Google Scholar 

  23. 23.

    Ball JR, Mitchell PB, Corry JC, Skillecorn A, Smith M, Malhi GS (2006) A randomized controlled trial of cognitive therapy for bipolar disorder: focus on long-term change. J Clin Psychiatry 67(2):277–286

    PubMed  Google Scholar 

  24. 24.

    Gonzalez IA, Echeburua E, Liminana JM, Gonzalez-Pinto A (2014) Psychoeducation and cognitive-behavioral therapy for patients with refractory bipolar disorder: a 5-year controlled clinical trial. Eur Psychiatry 29(3):134–141

    Google Scholar 

  25. 25.

    Zaretsky A, Lancee W, Miller C, Harris A, Parikh SV (2008) Is cognitive-behavioural therapy more effective than psychoeducation in bipolar disorder? Can J Psychiatry 53(7):441–448

    PubMed  Google Scholar 

  26. 26.

    Costa RT, Cheniaux E, Rosaes PA, Carvalho MR, Freire RC, Versiani M et al (2011) The effectiveness of cognitive behavioral group therapy in treating bipolar disorder: a randomized controlled study. Rev Bras Psiquiatr 33(2):144–149

    PubMed  Google Scholar 

  27. 27.

    Gonzalez Isasi A, Echeburua E, Liminana JM, Gonzalez-Pinto A (2014) Psychoeducation and cognitive-behavioral therapy for patients with refractory bipolar disorder: a 5-year controlled clinical trial. Eur Psychiatry 29(3):134–141

  28. 28.

    Fracalanza K, McCabe RE, Taylor VH, Antony MM (2014) The effect of comorbid major depressive disorder or bipolar disorder on cognitive behavioral therapy for social anxiety disorder. J Affect Disord 162:61–66

    PubMed  Google Scholar 

  29. 29.

    Hollandare F, Eriksson A, Lovgren L, Humble MB, Boersma K (2015) Internet-based cognitive behavioral therapy for residual symptoms in bipolar disorder type II: a single-subject design pilot study. JMIR Res Protoc 4(2):e44

    PubMed Central  PubMed  Google Scholar 

  30. 30.

    Jones SH, Smith G, Mulligan LD, Lobban F, Law H, Dunn G et al (2015) Recovery-focused cognitive-behavioural therapy for recent-onset bipolar disorder: randomised controlled pilot trial. Br J Psychiatry 206(1):58–66

    PubMed  Google Scholar 

  31. 31.

    Steinan MK, Krane-Gartiser K, Langsrud K, Sand T, Kallestad H, Morken G (2014) Cognitive behavioral therapy for insomnia in euthymic bipolar disorder: study protocol for a randomized controlled trial. Trials 15:24

    PubMed Central  PubMed  Google Scholar 

  32. 32.

    Peet M, Harvey NS (1991) Lithium maintenance: 1. A standard education programme for patients. Br J Psychiatry 158:197–200

    CAS  PubMed  Google Scholar 

  33. 33.

    Harvey NS, Peet M (1991) Lithium maintenance: 2. Effects of personality and attitude on health information acquisition and compliance. Br J Psychiatry 158:200–204

    CAS  PubMed  Google Scholar 

  34. 34.

    Dogan S, Sabanciogullari S (2003) The effects of patient education in lithium therapy on quality of life and compliance. Arch Psychiatr Nurs 17(6):270–275

    PubMed  Google Scholar 

  35. 35.

    Perry A, Tarrier N, Morriss R, McCarthy E, Limb K (1999) Randomised controlled trial of efficacy of teaching patients with bipolar disorder to identify early symptoms of relapse and obtain treatment. BMJ 318(7177):149–153

    CAS  PubMed Central  PubMed  Google Scholar 

  36. 36.

    Colom F, Vieta E, Sanchez-Moreno J, Palomino-Otiniano R, Reinares M, Goikolea JM et al (2009) Group psychoeducation for stabilised bipolar disorders: 5-year outcome of a randomised clinical trial. Br J Psychiatry 194(3):260–265

    CAS  PubMed  Google Scholar 

  37. 37.

    Colom F, Vieta E, Martinez-Aran A, Reinares M, Goikolea JM, Benabarre A et al (2003) A randomized trial on the efficacy of group psychoeducation in the prophylaxis of recurrences in bipolar patients whose disease is in remission. Arch Gen Psychiatry 60(4):402–407

    PubMed  Google Scholar 

  38. 38.

    Colom F, Vieta E, Reinares M, Martinez-Aran A, Torrent C, Goikolea JM et al (2003) Psychoeducation efficacy in bipolar disorders: beyond compliance enhancement. J Clin Psychiatry 64(9):1101–1105

    PubMed  Google Scholar 

  39. 39.

    Lobban F, Taylor L, Chandler C, Tyler E, Kinderman P, Kolamunnage-Dona R et al (2010) Enhanced relapse prevention for bipolar disorder by community mental health teams: cluster feasibility randomised trial. Br J Psychiatry 196(1):59–63

    CAS  PubMed  Google Scholar 

  40. 40.

    Colom F, Reinares M, Pacchiarotti I, Popovic D, Mazzarini L, Martinez AA et al (2010) Has number of previous episodes any effect on response to group psychoeducation in bipolar patients? Acta Neuropsychiatrica 22:50–53

    PubMed  Google Scholar 

  41. 41.

    Javadpour A, Hedayati A, Dehbozorgi GR, Azizi A (2013) The impact of a simple individual psycho-education program on quality of life, rate of relapse and medication adherence in bipolar disorder patients. Asian J Psychiatry 6(3):208–213

    Google Scholar 

  42. 42.

    Kurdal E, Tanriverdi D, Savas HA (2014) The effect of psychoeducation on the functioning level of patients with bipolar disorder. West J Nurs Res 36(3):312–328

    PubMed  Google Scholar 

  43. 43.

    Scott J, Colom F, Popova E, Benabarre A, Cruz N, Valenti M et al (2009) Long-term mental health resource utilization and cost of care following group psychoeducation or unstructured group support for bipolar disorders: a cost–benefit analysis. J Clin Psychiatry 70(3):378–386

    PubMed  Google Scholar 

  44. 44.

    Parikh SV, Zaretsky A, Beaulieu S, Yatham LN, Young LT, Patelis-Siotis I et al (2012) A randomized controlled trial of psychoeducation or cognitive-behavioral therapy in bipolar disorder: a Canadian Network for Mood and Anxiety treatments (CANMAT) study [CME]. J Clin Psychiatry 73(6):803–810

    PubMed  Google Scholar 

  45. 45.

    Smith DJ, Griffiths E, Poole R, di Florio A, Barnes E, Kelly MJ et al (2011) Beating bipolar: exploratory trial of a novel Internet-based psychoeducational treatment for bipolar disorder. Bipolar Disord 13(5–6):571–577

    PubMed  Google Scholar 

  46. 46.

    Proudfoot J, Parker G, Manicavasagar V, Hadzi-Pavlovic D, Whitton A, Nicholas J et al (2012) Effects of adjunctive peer support on perceptions of illness control and understanding in an online psychoeducation program for bipolar disorder: a randomised controlled trial. J Affect Disord 142(1–3):98–105

    PubMed  Google Scholar 

  47. 47.

    Castle D, White C, Chamberlain J, Berk M, Berk L, Lauder S et al (2010) Group-based psychosocial intervention for bipolar disorder: randomised controlled trial. Br J Psychiatry 196(5):383–388

    PubMed  Google Scholar 

  48. 48.

    van der Voort TY, van Meijel B, Goossens PJ, Hoogendoorn AW, Draisma S, Beekman A et al (2015) Collaborative care for patients with bipolar disorder: randomised controlled trial. Br J Psychiatry 206(5):393–400

    PubMed  Google Scholar 

  49. 49.

    Fiorillo A, Del Vecchio V, Luciano M, Sampogna G, De Rosa C, Malangone C et al (2014) Efficacy of psychoeducational family intervention for bipolar I disorder: a controlled, multicentric, real-world study. J Affect Disord 172C:291–299

    PubMed  Google Scholar 

  50. 50.

    Bauer MS, McBride L, Williford WO, Glick H, Kinosian B, Altshuler L et al (2006) Collaborative care for bipolar disorder: part II. Impact on clinical outcome, function, and costs. Psychiatr Serv 57(7):937–945

  51. 51.

    Simon GE, Ludman EJ, Bauer MS, Unutzer J, Operskalski B (2006) Long-term effectiveness and cost of a systematic care program for bipolar disorder. Arch Gen Psychiatry 63(5):500–508

    PubMed  Google Scholar 

  52. 52.

    Eker F, Harkin S (2012) Effectiveness of six-week psychoeducation program on adherence of patients with bipolar affective disorder. J Affect Disord 138(3):409–416

    PubMed  Google Scholar 

  53. 53.

    Faria AD, de Mattos Souza LD, de Azevedo Cardoso T, Pinheiro KA, Pinheiro RT, da Silva RA et al (2014) The influence of psychoeducation on regulating biological rhythm in a sample of patients with bipolar II disorder: a randomized clinical trial. Psychol Res Behav Manag 7:167–174

    PubMed Central  PubMed  Google Scholar 

  54. 54.

    de Cardoso TA, de Farias CA, Mondin TC, da Silva GDG, Souza LD, da Silva RA et al (2014) Brief psychoeducation for bipolar disorder: impact on quality of life in young adults in a 6-month follow-up of a randomized controlled trial. Psychiatry Res 220(3):896–902

  55. 55.

    Cuhadar D, Cam MO (2014) Effectiveness of psychoeducation in reducing internalized stigmatization in patients with bipolar disorder. Arch Psychiatr Nurs 28(1):62–66

    PubMed  Google Scholar 

  56. 56.

    Todd NJ, Jones SH, Hart A, Lobban FA (2014) A web-based self-management intervention for bipolar disorder ‘living with bipolar’: a feasibility randomised controlled trial. J Affect Disord 169:21–29

    PubMed  Google Scholar 

  57. 57.

    Barnes CW, Hadzi-Pavlovic D, Wilhelm K, Mitchell PB (2015) A web-based preventive intervention program for bipolar disorder: outcome of a 12-months randomized controlled trial. J Affect Disord 174:485–492

    PubMed  Google Scholar 

  58. 58.

    Depp CA, Ceglowski J, Wang VC, Yaghouti F, Mausbach BT, Thompson WK et al (2015) Augmenting psychoeducation with a mobile intervention for bipolar disorder: a randomized controlled trial. J Affect Disord 174:23–30

    PubMed  Google Scholar 

  59. 59.

    Bond K, Anderson IM (2015) Psychoeducation for relapse prevention in bipolar disorder: a systematic review of efficacy in randomized controlled trials. Bipolar Disord 17(4):349–362

    PubMed  Google Scholar 

  60. 60.

    Frank E, Kupfer DJ, Thase ME, Mallinger AG, Swartz HA, Fagiolini AM et al (2005) Two-year outcomes for interpersonal and social rhythm therapy in individuals with bipolar I disorder. Arch Gen Psychiatry 62(9):996–1004

    PubMed  Google Scholar 

  61. 61.

    Frank E, Soreca I, Swartz HA, Fagiolini AM, Mallinger AG, Thase ME et al (2008) The role of interpersonal and social rhythm therapy in improving occupational functioning in patients with bipolar I disorder. Am J Psychiatry 165(12):1559–1565

    PubMed Central  PubMed  Google Scholar 

  62. 62.

    Swartz HA, Frank E, Cheng Y (2012) A randomized pilot study of psychotherapy and quetiapine for the acute treatment of bipolar II depression. Bipolar Disord 14(2):211–216

    CAS  PubMed Central  PubMed  Google Scholar 

  63. 63.

    Inder ML, Crowe MT, Luty SE, Carter JD, Moor S, Frampton CM et al (2015) Randomized, controlled trial of Interpersonal and Social Rhythm Therapy for young people with bipolar disorder. Bipolar Disord 17(2):128–138

    PubMed  Google Scholar 

  64. 64.

    van Gent EM, Zwart FM (1991) Psychoeducation of partners of bipolar-manic patients. J Affect Disord 21(1):15–18

    PubMed  Google Scholar 

  65. 65.

    Miklowitz DJ, Simoneau TL, George EL, Richards JA, Kalbag A, Sachs-Ericsson N et al (2000) Family-focused treatment of bipolar disorder: 1-year effects of a psychoeducational program in conjunction with pharmacotherapy. Biol Psychiatry 48(6):582–592

    CAS  PubMed  Google Scholar 

  66. 66.

    Miklowitz DJ, George EL, Richards JA, Simoneau TL, Suddath RL (2003) A randomized study of family-focused psychoeducation and pharmacotherapy in the outpatient management of bipolar disorder. Arch Gen Psychiatry 60(9):904–912

    PubMed  Google Scholar 

  67. 67.

    Rea MM, Tompson MC, Miklowitz DJ, Goldstein MJ, Hwang S, Mintz J (2003) Family-focused treatment versus individual treatment for bipolar disorder: results of a randomized clinical trial. J Consult Clin Psychol 71(3):482–492

    PubMed  Google Scholar 

  68. 68.

    Scott J, Colom F, Pope M, Reinares M, Vieta E (2012) The prognostic role of perceived criticism, medication adherence and family knowledge in bipolar disorders. J Affect Disord 142(1–3):72–76

    PubMed  Google Scholar 

  69. 69.

    Clarkin JF, Carpenter D, Hull J, Wilner P, Glick I (1998) Effects of psychoeducational intervention for married patients with bipolar disorder and their spouses. Psychiatr Serv 49(4):531–533

    CAS  PubMed  Google Scholar 

  70. 70.

    Miller IW, Keitner GI, Ryan CE, Uebelacker LA, Johnson SL, Solomon DA (2008) Family treatment for bipolar disorder: family impairment by treatment interactions. J Clin Psychiatry 69(5):732–740

    PubMed Central  PubMed  Google Scholar 

  71. 71.

    Solomon DA, Keitner GI, Ryan CE, Kelley J, Miller IW (2008) Preventing recurrence of bipolar I mood episodes and hospitalizations: family psychotherapy plus pharmacotherapy versus pharmacotherapy alone. Bipolar Disord 10(7):798–805

    PubMed  Google Scholar 

  72. 72.

    Reinares M, Colom F, Sanchez-Moreno J, Torrent C, Martinez-Aran A, Comes M et al (2008) Impact of caregiver group psychoeducation on the course and outcome of bipolar patients in remission: a randomized controlled trial. Bipolar Disord 10(4):511–519

    PubMed  Google Scholar 

  73. 73.

    Reinares M, Vieta E, Colom F, Martinez-Aran A, Torrent C, Comes M et al (2004) Impact of a psychoeducational family intervention on caregivers of stabilized bipolar patients. Psychother Psychosom 73(5):312–319

    CAS  PubMed  Google Scholar 

  74. 74.

    Madigan K, Egan P, Brennan D, Hill S, Maguire B, Horgan F et al (2012) A randomised controlled trial of carer-focussed multi-family group psychoeducation in bipolar disorder. Eur Psychiatry 27(4):281–284

    CAS  PubMed  Google Scholar 

  75. 75.

    Perlick DA, Miklowitz DJ, Lopez N, Chou J, Kalvin C, Adzhiashvili V et al (2010) Family-focused treatment for caregivers of patients with bipolar disorder. Bipolar Disord 12(6):627–637

    PubMed Central  PubMed  Google Scholar 

  76. 76.

    D’Souza R, Piskulic D, Sundram S (2010) A brief dyadic group based psychoeducation program improves relapse rates in recently remitted bipolar disorder: a pilot randomised controlled trial. J Affect Disord 120(1–3):272–276

    PubMed  Google Scholar 

  77. 77.

    Fredman SJ, Baucom DH, Boeding SE, Miklowitz DJ (2015) Relatives’ emotional involvement moderates the effects of family therapy for bipolar disorder. J Consult Clin Psychol 83(1):81–91

    PubMed  Google Scholar 

  78. 78.

    Miklowitz DJ, Otto MW, Frank E, Reilly-Harrington NA, Wisniewski SR, Kogan JN et al (2007) Psychosocial treatments for bipolar depression: a 1-year randomized trial from the Systematic Treatment Enhancement Program. Arch Gen Psychiatry 64(4):419–426

    PubMed Central  PubMed  Google Scholar 

  79. 79.

    Miklowitz DJ, Otto MW, Frank E, Reilly-Harrington NA, Kogan JN, Sachs GS et al (2007) Intensive psychosocial intervention enhances functioning in patients with bipolar depression: results from a 9-month randomized controlled trial. Am J Psychiatry 164(9):1340–1347

    PubMed Central  PubMed  Google Scholar 

  80. 80.

    Deckersbach T, Nierenberg AA, Kessler R, Lund HG, Ametrano RM, Sachs G et al (2010) RESEARCH: cognitive rehabilitation for bipolar disorder: an open trial for employed patients with residual depressive symptoms. CNS Neurosci Ther 16(5):298–307

    PubMed Central  PubMed  Google Scholar 

  81. 81.

    Martinez-Aran A, Torrent C, Sole B, Bonnin CM, Rosa AR, Sanchez-Moreno J et al (2011) Functional remediation for bipolar disorder. Clin Pract Epidemiol Ment Health 7:112–116

  82. 82.

    Torrent C, Bonnin CM, Martinez-Aran A, Valle J, Amann BL, Gonzalez-Pinto A et al (2013) Efficacy of functional remediation in bipolar disorder: a multicenter randomized controlled study. Am J Psychiatry 170(8):852–859

    PubMed  Google Scholar 

  83. 83.

    Lahera G, Benito A, Montes JM, Fernandez-Liria A, Olbert CM, Penn DL (2013) Social cognition and interaction training (SCIT) for outpatients with bipolar disorder. J Affect Disord 146(1):132–136

    CAS  PubMed  Google Scholar 

  84. 84.

    Sole B, Bonnin CM, Mayoral M, Amann BL, Torres I, Gonzalez-Pinto A et al (2015) Functional remediation for patients with bipolar II disorder: improvement of functioning and subsyndromal symptoms. Eur Neuropsychopharmacol 25(2):257–264

    CAS  PubMed  Google Scholar 

  85. 85.

    Williams JM, Alatiq Y, Crane C, Barnhofer T, Fennell MJ, Duggan DS et al (2008) Mindfulness-based cognitive therapy (MBCT) in bipolar disorder: preliminary evaluation of immediate effects on between-episode functioning. J Affect Disord 107(1–3):275–279

    CAS  PubMed Central  PubMed  Google Scholar 

  86. 86.

    Ives-Deliperi VL, Howells F, Stein DJ, Meintjes EM, Horn N (2013) The effects of mindfulness-based cognitive therapy in patients with bipolar disorder: a controlled functional MRI investigation. J Affect Disord 150(3):1152–1157

    PubMed  Google Scholar 

  87. 87.

    Perich T, Manicavasagar V, Mitchell PB, Ball JR, Hadzi-Pavlovic D (2013) A randomized controlled trial of mindfulness-based cognitive therapy for bipolar disorder. Acta Psychiatr Scand 127(5):333–343

    CAS  PubMed  Google Scholar 

  88. 88.

    Perich T, Manicavasagar V, Mitchell PB, Ball JR (2013) The association between meditation practice and treatment outcome in mindfulness-based cognitive therapy for bipolar disorder. Behav Res Ther 51(7):338–343

    PubMed  Google Scholar 

  89. 89.

    Howells FM, Ives-Deliperi VL, Horn NR, Stein DJ (2012) Mindfulness based cognitive therapy improves frontal control in bipolar disorder: a pilot EEG study. BMC Psychiatry 12:15

    PubMed Central  PubMed  Google Scholar 

  90. 90.

    Stange JP, Eisner LR, Holzel BK, Peckham AD, Dougherty DD, Rauch SL et al (2011) Mindfulness-based cognitive therapy for bipolar disorder: effects on cognitive functioning. J Psychiatr Pract 17(6):410–419

    PubMed Central  PubMed  Google Scholar 

  91. 91.

    Van DS, Jeffrey J, Katz MR (2013) A randomized, controlled, pilot study of dialectical behavior therapy skills in a psychoeducational group for individuals with bipolar disorder. J Affect Disord 145(3):386–393

    Google Scholar 

  92. 92.

    Bos EH, Merea R, van den Brink E, Sanderman R, Bartels-Velthuis AA (2014) Mindfulness training in a heterogeneous psychiatric sample: outcome evaluation and comparison of different diagnostic groups. J Clin Psychol 70(1):60–71

    PubMed  Google Scholar 

  93. 93.

    Colom F, Vieta E, Sanchez-Moreno J, Martinez-Aran A, Reinares M, Goikolea JM et al (2005) Stabilizing the stabilizer: group psychoeducation enhances the stability of serum lithium levels. Bipolar Disord 7(Suppl 5):32–36

    PubMed  Google Scholar 

  94. 94.

    Simoneau B, Lavallee P, Anderson PC, Bailey M, Bantle G, Berthiaume S et al (1999) Discovery of non-peptidic P2-P3 butanediamide renin inhibitors with high oral efficacy. Bioorg Med Chem 7(3):489–508

    CAS  PubMed  Google Scholar 

  95. 95.

    Scott J, Colom F, Vieta E (2007) A meta-analysis of relapse rates with adjunctive psychological therapies compared to usual psychiatric treatment for bipolar disorders. Int J Neuropsychopharmacol 10(1):123–129

    CAS  PubMed  Google Scholar 

  96. 96.

    Reinares M, Colom F, Rosa AR, Bonnin CM, Franco C, Sole B et al (2010) The impact of staging bipolar disorder on treatment outcome of family psychoeducation. J Affect Disord 123(1–3):81–86

    PubMed  Google Scholar 

  97. 97.

    Lam DH, Burbeck R, Wright K, Pilling S (2009) Psychological therapies in bipolar disorder: the effect of illness history on relapse prevention—a systematic review. Bipolar Disord 11(5):474–482

    PubMed  Google Scholar 

  98. 98.

    Kapczinski F, Dias VV, Kauer-Sant’Anna M, Frey BN, Grassi-Oliveira R, Colom F et al (2009) Clinical implications of a staging model for bipolar disorders. Expert Rev Neurother 9(7):957–966

    PubMed  Google Scholar 

  99. 99.

    Berk M, Conus P, Lucas N, Hallam K, Malhi GS, Dodd S et al (2007) Setting the stage: from prodrome to treatment resistance in bipolar disorder. Bipolar Disord 9(7):671–678

    PubMed  Google Scholar 

  100. 100.

    Miklowitz DJ, Axelson DA, George EL, Taylor DO, Schneck CD, Sullivan AE et al (2009) Expressed emotion moderates the effects of family-focused treatment for bipolar adolescents. J Am Acad Child Adolesc Psychiatry 48(6):643–651

    PubMed  Google Scholar 

  101. 101.

    Vieta E (2010) Individualizing treatment for patients with schizoaffective disorder. J Clin Psychiatry 71(10):e26

    PubMed  Google Scholar 

  102. 102.

    Murru A, Pacchiarotti I, Nivoli AM, Colom F, Vieta E (2012) Is schizoaffective disorder still a neglected condition in the scientific literature? Psychother Psychosom 81(6):389–390

    PubMed  Google Scholar 

  103. 103.

    Fountoulakis KN, Gonda X, Siamouli M, Rihmer Z (2009) Psychotherapeutic intervention and suicide risk reduction in bipolar disorder: a review of the evidence. J Affect Disord 113(1–2):21–29

    PubMed  Google Scholar 

  104. 104.

    Fountoulakis KN, Siamouli M (2009) Re: how well do psychosocial interventions work in bipolar disorder? Can J Psychiatry 54(8):578

    PubMed  Google Scholar 

  105. 105.

    Weiss RD, Griffin ML, Kolodziej ME, Greenfield SF, Najavits LM, Daley DC et al (2007) A randomized trial of integrated group therapy versus group drug counseling for patients with bipolar disorder and substance dependence. Am J Psychiatry 164(1):100–107

    PubMed  Google Scholar 

  106. 106.

    Weiss RD, Griffin ML, Jaffee WB, Bender RE, Graff FS, Gallop RJ et al (2009) A “community-friendly” version of integrated group therapy for patients with bipolar disorder and substance dependence: a randomized controlled trial. Drug Alcohol Depend 104(3):212–219

    PubMed Central  PubMed  Google Scholar 

  107. 107.

    Gonzalez-Isasi A, Echeburua E, Mosquera F, Ibanez B, Aizpuru F, Gonzalez-Pinto A (2010) Long-term efficacy of a psychological intervention program for patients with refractory bipolar disorder: a pilot study. Psychiatry Res 176(2–3):161–165

    PubMed  Google Scholar 

  108. 108.

    Lam D, Donaldson C, Brown Y, Malliaris Y (2005) Burden and marital and sexual satisfaction in the partners of bipolar patients. Bipolar Disord 7(5):431–440

    PubMed  Google Scholar 

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Authors’ contributions

KNF SM, SM and ET carried out the literature search and the interpretation of the results. KNF wrote the first draft and all the other authors contributed to the revision including the final draft. All authors read and approved the final manuscript.

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Correspondence to Konstantinos N Fountoulakis.

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Miziou, S., Tsitsipa, E., Moysidou, S. et al. Psychosocial treatment and interventions for bipolar disorder: a systematic review. Ann Gen Psychiatry 14, 19 (2015).

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  • Bipolar Disorder
  • Bipolar Disorder Patient
  • Mood Episode
  • Cognitive Remediation
  • Group Psychoeducation