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Family-based interpersonal psychotherapy (FB-IPT) is a developmental adaptation of Interpersonal Psychotherapy for Depressed Adolescent (IPT-A) and an evidence-based psychological intervention for treating depression in preadolescent children between the ages of 8–12. This chapter describes the developmental issues related to early-onset depression in children 12 and younger, and the interpersonal risk and protective factors that contribute to depressive symptoms in preteens. This chapter outlines the structure and goals of the 14-session intervention, as well as the developmental adaptations in FB-IPT, including increasing the frequency of parent and parent–child meetings, expanding the limited sick role for parents and adding a set of Parent Tips, an increased focus on comorbid anxiety symptoms and adding visuals to the mood rating scale, communication analysis and decision analysis. A detailed case study utilising FB-IPT with a depressed preadolescent and parent demonstrates the real-life application of this psychological treatment and highlights common challenges in implementing FB-IPT. The chapter wraps up with a discussion of the clinical studies that have supported the development and preliminary efficacy of FB-IPT and suggestions for future directions and areas of dissemination.
Demand for child and adolescent mental health support is rising, with long waits risking deterioration. The Lucy Project provides rapid, self–referral, low–intensity CBT (LICBT) within paediatric settings, with interventions taking place via video call. While previous work suggests good reach and outcomes, equity of access and acceptability across demographic groups requires evaluation. This paper examines whether socioeconomic status (SES) and ethnicity are associated with engagement with the service. Service records for 149 patients referred to The Lucy Project in Sheffield Children’s Hospital between December 2022 and December 2024 were analysed. Engagement (engaged vs not–engaged) was recorded, and this was analysed in the context of ethnicity (White British; other; unknown) and indices of multiple deprivation (IMD) decile. Binary logistic regression tested associations. The sample’s ethnicity was broadly similar to that of the general population where the service is based; 27.5% lived in the two most deprived IMD deciles (vs 34.2% citywide). Ethnicity did not predict engagement, whereas IMD decile was shown to be associated with engagement. Results suggested that the more affluent a patient, the more likely they were to drop out. In this video-based, self–referral LICBT service, engagement did not differ by ethnicity but was higher among children and young people from more deprived areas. Findings support the model’s potential to mitigate socioeconomic barriers post–referral, while highlighting the need to optimise engagement for more affluent families and to continue addressing pre–referral inequities and digital exclusion.
Key learning aims
(1) To Understand the context of the implementation of The Lucy Project, a self-referral low-intensity cognitive behavioural therapy service in a paediatric setting.
(2) To explore the relationship between experiences of deprivation and its impact on engagement with The Lucy Project.
(3) To explore the relationships between ethnicity and engagement with The Lucy Project.
(4) To explore potential pros and cons of a self-referral mental health service in a paediatric setting.
Exposure to stress is a well-established risk factor for psychotic experiences, yet the cognitive mechanisms underlying this association remain insufficiently understood. This study examined whether longitudinal changes in cognitive biases mediate the relationship between stress exposure and changes in psychotic-like experiences (PLEs) in the general population sample of adults aged 18–40 years.
Methods
Adults without a history of psychiatric treatment were assessed at baseline and at 12-month follow-up. Change-score mediation models with bootstrap confidence intervals were estimated, adjusting for age, gender, and education.
Results
Of 5,126 adults who completed the baseline assessment, 2,290 (44.7%) participated in the follow-up. Greater stress exposure predicted increases in PLEs, negative, and depressive symptoms. After correction for multiple testing, significant indirect effects consistent with mediation by cognitive biases were observed for PLEs, but not for negative or depressive symptoms. These effects were significant for changes in belief inflexibility, safety behaviors, external attribution, and subjective cognitive and social cognitive problems, but not for attention to threat or jumping to conclusions. Reverse mediation models indicated consistently smaller indirect effects. In parallel multiple-mediator models, no individual bias showed a unique indirect effect on PLEs, yet the total indirect effect remained significant, suggesting mediation through interrelated biases. Social cognitive problems emerged as the only bias with a specific indirect effect on negative and depressive symptoms.
Conclusions
Longitudinal changes in cognitive biases might represent an indirect pathway to the association between stress exposure and increases in PLEs. These findings highlight cognitive biases as potential targets for preventive interventions.
Early intervention increases the likelihood of eating disorder recovery but many young people delay help-seeking. We developed a smartphone-friendly, online decision-making tool to address this gap (FREED-Mobile (FREED-M)).
Aims
To conduct a randomised controlled feasibility trial of the FREED-M decision-making tool with 16- to 25-year-olds with a suspected eating disorder and no previous treatment for this.
Method
Participants were randomly allocated to FREED-M or an active control in a parallel group, two-arm trial. Outcomes were measured at weeks 0 (baseline), 4 (post-intervention) and 12 (follow-up). The primary feasibility outcome was attrition at follow-up. Other outcomes included motivational, clinical and economic measures.
Results
We over-recruited with 204 randomised participants (including 20 fraudulent participants). Main analyses were conducted with 184 genuine responders (FREED-M: n = 91, control: n = 93). At baseline, participants’ mean age was 21.0 (s.d. 2.0) years, 89% identified as female and 64% as White. Mean body mass index was 23.1 kg/m2 (6.3). N = 83 participants had an anorexia nervosa-like disorder, 101 had another eating disorder or high eating disorder risk. Attrition at week 12 was n = 112 (61%). Of the n = 42 FREED-M participants who provided acceptability ratings, 79% liked the intervention and 66% found it useful. Between-group effect sizes for motivation and readiness to change were small to medium at 4 weeks (d = 0.27 and d = 0.15, respectively) favouring FREED-M, but differences were not sustained at follow-up (d = −0.02 and d = −0.12, respectively).
Discussions
Although the attrition rate was high, recruitment exceeded expectations. Acceptability of FREED-M was high among participants who provided acceptability ratings. Motivation/readiness to change and help-seeking are candidates for primary outcomes in a future randomised controlled trial.
The 7 October 2023, terrorist attack at the Nova Festival in southern Israel caused deaths, injuries, hostage-taking and prolonged life-threatening exposure, creating an urgent need for early interventions to reduce post-traumatic morbidity. Although prolonged exposure is an established post-traumatic stress disorder (PTSD) treatment, its feasibility and benefit during ongoing threat remain unclear.
Aims
This preliminary study evaluated a war-adapted brief prolonged exposure protocol (WBPE) delivered shortly after trauma in Nova Festival survivors with acute stress disorder.
Method
Forty survivors completed the WBPE and were assessed at baseline and immediately post treatment. A subsample of 27 WBPE completers and 18 untreated wait-list controls was reassessed after 5 months. Outcomes were PTSD (PDS-5), depression (PHQ-9) and anxiety (GAD-7) symptom severity.
Results
WBPE was associated with significant reductions in PTSD, depression and anxiety immediately after treatment. At 5 months, WBPE participants showed greater reductions in PTSD and depressive symptom severity and lower PTSD and depression symptom scores than controls, with large effect sizes. Anxiety symptoms improved in both groups, consistent with possible natural recovery. Clinically significant depressive symptoms (48.15 v. 77.78%) and anxiety symptoms (37.04 v. 72.22%) were less frequent in WBPE participants than controls, whereas probable PTSD rates did not differ significantly. Substance use during the study period was associated with poorer outcomes and smaller symptom reductions.
Conclusions
WBPE appears feasible and potentially beneficial under wartime conditions, with meaningful improvements in PTSD and depression despite persistent threat. Substance use was linked to poorer recovery and should be systematically assessed in post-trauma care.
Young people (YP) face numerous challenges that can lead to mental health difficulties, yet mental health systems worldwide are often unprepared to support those affected. Club Synergy, a low-threshold, trauma-informed digital and face-to-face service for YP aged 14–25 with emotional and/or behavioural difficulties, was established in Georgia in 2019. This study examined the characteristics, clinical effectiveness and outcome predictors of YP presenting to Synergy. Quantitative data, including clinical outcome measures and treatment details, were collected pre- and post-treatment and at three-month follow-up over a 21-month period (November 2019–July 2021). Of 266 YP who completed treatment, most were female (66.9%; mean age 19.95, SD 3.13). Common presenting difficulties included emotional instability (77.1%), anxiety and restlessness (63.5%), interpersonal problems (53%) and low mood (48.5%). Among 144 who completed the ACEs measure, 57.6% reported four or more adverse childhood experiences. Most (67.7%) received transdiagnostic programmes; 74.1% of these completed the Emotional Regulation module (mean 7.18 sessions, SD 7.23). Significant reductions in depression and anxiety, and improved functioning, were observed post-treatment and at follow-up (p < 0.01). Quality-of-life gains were not sustained at follow-up (p = 0.14). Satisfaction was high (94.8%). Trauma-informed, transdiagnostic services grounded in a biopsychosocial model appear acceptable and potentially beneficial for YP at risk of or experiencing common mental health symptoms.
Functional impairment in psychosis often persists despite symptomatic remission. There is a paucity of research examining early-course psychosocial functioning trajectories, and none has been conducted to examine relationship between the trajectories and prospective long-term functional outcomes in early psychosis sample.
Methods
We conducted 12-year follow-up of a randomized controlled trial on extended early intervention for first-episode psychosis to identify early-course social-occupational functioning trajectories and their baseline predictors and associations with 12-year outcomes. Participants who completed Social and Occupational Functioning Scale (SOFAS) scores at three or more timepoints between baseline and 3-year follow-up were included in the study. Premorbid adjustment, illness characteristics, symptom severity, functioning, and treatment profiles were assessed. Latent growth mixture modeling was employed to derive early-course social-occupational functioning trajectories based on SOFAS scores over 3-year follow-up.
Results
A total of 148 participants were included in this study, with 106 patients having completed the 12-year follow-up. Our results identified four distinct trajectories, including persistently-good class, gradually-improved class, suboptimal-stable class, and persistently-poor class. Patients in persistently-poor class had more severe negative symptoms at baseline compared to patients in persistently-good class. Patients with persistently-poor trajectory had worse long-term outcomes than those with other classes in the majority of functional measures at 12-year follow-up.
Conclusions
The majority of patients were classified in early-stage suboptimal or poor functional trajectories. Above one-fourth of the participants exhibited persistently-poor social-occupational functioning trajectory, which predicted worse functional outcomes at 12-year follow-up. These findings highlighted the importance of tracking functional changes during the initial years of illness.
Cerebral palsy (CP) is a heterogeneous group of motor disorders resulting from nonprogressive brain disturbances. This chapter presents two case studies: One infant born prematurely with left hemiplegia, who actively participates in sports and attends mainstream school, and a second infant, born at full-term diagnosed with CP due to increased lower limb tone and mobility challenges. These cases illustrate the importance of timely diagnosis and early intervention to enhance functional outcomes. The discussion emphasizes the significance of comprehensive assessments, multidisciplinary management strategies, and the evolving understanding of CP definitions, highlighting the potential for improved quality of life through targeted interventions.
Neonatal brain injury can have impact on long-term functional outcomes. Intraventricular hemorrhage is associated with neurodevelopmental impairment (cerebral palsy, cognitive or language delay, and vision or hearing impairment) at age 2 years. Risk of significant impairment is increased by severity of hemorrhage, posthemorrhagic hydrocephalus, and white matter injury. Infants experiencing perinatal stroke most commonly face motor impairments in early childhood and beyond. Injury from hypoxia–ischemia may lead to motor delays, cognitive impairment, and behavioral challenges. Brain injury during the neonatal period can alter developmental trajectories, causing functional impairment, limitations in peer and community participation, and significant family distress. Despite this, the infant nervous system is incredibly plastic and resilient. The neonatal period is a time of active synaptogenesis and the building of larger neural networks through which to acquire motor, cognitive, and language skills. Brain injury can disrupt this process. Yet infants also display a remarkable ability to recover, adapt, and (re)gain functional abilities due to the robust developmental activity of the immature nervous system. Outcomes largely depend on injury location and extent, and environmental context. Brain injury developmental impact can be exacerbated by concomitant social adversity. Treatment delays must be identified early, and effective directed interventions initiated.
The possibility of achieving an accurate and early diagnosis of cerebral palsy has become a reality and is now considered the standard of care. The shift toward early diagnosis has catalyzed the initiation of numerous clinical trials within the first 2 years of life, yielding emerging data on effective interventions. This research confirms the long-held belief in the critical importance of specialist intervention beginning before 6 months of age. The accumulation of evidence is rapidly reshaping the landscape of cerebral palsy diagnosis and early intervention knowledge, ultimately influencing child outcomes. Parents harbor hope that this earlier targeted treatment approach will yield improved outcomes for their children, and emerging data suggest that this optimism is well founded. As we continue to advance our understanding and refine our practices, the future holds promise for further enhancing the lives of individuals affected by cerebral palsy.
Executive function (EF) deficits are consistently linked to psychopathology symptoms, though the mechanisms linking poor EF to symptom expression remain unclear.
Methods
The study used the Research Domain Criteria (RDoC) approach to examine relationships between teacher-reported latent psychopathology symptoms, including a general psychopathology factor (P-Factor), and EF in young children with emerging mental health problems. Participants were 804 children (70.8% male; aged 49–89 months) referred by their teachers for cognitive, emotional, or behavioral problems at school. To assess psychopathology, teachers completed the Strengths and Difficulties Questionnaire (SDQ). EF measures included inhibition, cognitive flexibility, working memory, sustained attention, and episodic memory, assessed using the NIH Toolbox, Automated Working Memory Assessment, and the Amsterdam Neuropsychological Test battery.
Results
Structural equation modeling (incorporating confirmatory factor analysis) showed reasonable model fit and supported a P-Factor structure. Correlational analyses explored EF–psychopathology associations, followed by a sensitivity analysis controlling for sex. We observed patterns of cognitive processes that showed inverse associations between EF performance and specific clinical problems. Sustained attention was positively associated with emotional problems but negatively associated with hyperactivity problems. Sex-stratified analyses revealed distinct patterns, with inhibition problems strongly linked to conduct and hyperactivity problems, but in females only.
Conclusions
The findings support poor EF as a transdiagnostic risk factor associated with incremental vulnerability for childhood psychopathology. Divergent findings for sustained attentional processes suggest they can be adaptive in some contexts but maladaptive in others. Screening for EF difficulties in children could enhance early identification and inform interventions.
Extreme hot weather poses increasing risks to mental health. Yet, factors affecting vulnerability are under-researched. This mixed-method study integrates a systematic review and qualitative investigation to identify risk and protective factors for heat-related mental health issues, leading to the co-development of a screening tool. This could inform future research and, pending validation in clinical settings, support mental health professionals in assessing vulnerability among service users.
Methods
We searched PubMed and Web of Science for publications on extreme heat, mental health, and risk/protective factors. In addition, we conducted six focus groups with 21 people with lived experience of heat and/or mental illness and 12 healthcare professionals. Transcripts were analyzed using thematic content analysis and informed the co-development of the screening tool.
Results
Out of 764 articles identified by the systematic review, 47 were included. Evidence emerged for age, sex, existing mental illness, ethnicity, and socioeconomic status as risk factors. However, findings were inconsistent between studies, likely due to differences in study population and methodology. Protective effects included good physical health, social support, and exposure to green spaces. Our qualitative investigation identified additional risk and protective factors related to: (1) behavioral adaptability, (2) personal heat sensitivity, and (3) disparities in heat exposure. The resulting screening tool, HEAT-MH (Heat Exposure Assessment Tool for Mental Health), contains 15 questions on previous experiences of heat, general health, and lifestyle.
Conclusions
The mental health impacts of extreme heat depend on a range of risk and protective factors, including demographic, socioeconomic, health, and lifestyle characteristics.
Psychotic-like experiences (PLEs) are common in adolescence and often associated with later mental health difficulties. Although many psychosocial factors are related to PLEs, little is known about how these factors interact over time. Longitudinal network analysis allows examination of the stability of symptom associations and identification of potential intervention targets. This study investigated the structure and temporal stability of PLE networks in a large community-based adolescent cohort.
Methods
Adolescents aged 13–19 years (N = 605 with complete data across all time points) completed assessments at baseline, 12 months, and 24 months. Measures included positive and negative PLEs, cognitive biases, depression, anxiety, trauma, and interpersonal sensitivity. Networks were estimated at each time point, and permutation-based tests were used to compare network structure and overall connectivity across time. Centrality stability was assessed using bootstrapping procedures.
Results
Network structures were stable across the 2-year period, with no significant differences in overall organization or connectivity between time points. Depression consistently showed the highest centrality, followed by anxiety and attributional bias. Positive PLEs were most strongly associated with anxiety, while negative PLEs showed their strongest associations with depression. Attributional bias remained centrally positioned and was strongly linked to trauma. All networks showed robust accuracy and high stability.
Conclusions
Despite considerable developmental change during adolescence, the psychosocial architecture of PLEs remained notably stable. Depression, anxiety, and attributional biases emerged as consistent key nodes, highlighting them as promising targets for prevention and early intervention in adolescents at risk for persistent PLEs.
Edited by
Katherine Warburton, California Department of State Hospitals, University of California, Davis, USA,Stephen M. Stahl, University of California, Riverside, USA
This chapter explores the transformative potential of early intervention in schizophrenia, emphasizing its role in improving clinical, functional, and social outcomes. Through the poignant case of “Roger,” a man whose life was marked by untreated psychosis, homelessness, and missed opportunities for care, the chapter illustrates the consequences of delayed treatment and fragmented systems. It reviews epidemiological data, the importance of reducing the duration of untreated psychosis (DUP), and the neurobiological rationale for early-phase treatment. Models such as Coordinated Specialty Care (CSC), EPPIC, and Assertive Community Treatment (ACT) are discussed as effective frameworks for delivering comprehensive, multidisciplinary care. The chapter also addresses barriers to early intervention—including stigma, misdiagnosis, access limitations, and systemic inequities—and advocates for integrated, culturally responsive, and person-centered approaches. Ultimately, it calls for a shift in healthcare systems to prioritize early identification and treatment as a moral and clinical imperative.
Restrictive interventions are used in the treatment of some people with severe mental disorders such as psychosis – including psychiatric intensive care unit (PICU) admission, seclusion and restraint. Early Intervention in Psychosis (EIP) service input may improve outcomes in psychosis, but it is unclear whether specific components of EIP care reduce the need for restrictive practice.
Aims
To examine associations between EIP care components, demographic characteristics and restrictive interventions.
Method
We conducted a retrospective cohort study of 14 874 people who used EIP services in England, using linked data from the National Clinical Audit of Psychosis and the Mental Health Services Data Set. We examined associations between EIP components and time to PICU admission (primary outcome) alongside seclusion/physical restraint/injected chemical restraint/requests for police assistance (secondary outcomes), using multilevel Cox regression, adjusting for demographic factors and clustering by service.
Results
Higher hazards of restrictive interventions were observed among men, younger people and several minority ethnic groups. Individuals eligible for clozapine who were not offered it (hazard ratio 1.51, 95% CI 1.20–1.91) or refused it (hazard ratio 1.46, 95% CI 1.02–2.10) had higher hazards of PICU admission than those not eligible, whereas those who were eligible for clozapine and received it did not. There was weaker evidence of similar effects on hazards of physical restraint and seclusion. Receipt of CBT for psychosis was associated with reduced hazards of PICU admission (hazard ratio 0.80, 95% CI 0.67–0.95) and physical restraint (hazard ratio 0.68, 95% CI 0.47–0.98). Substance use was associated with increased hazards of PICU admission and requests for police assistance, although substance use interventions appeared to partially mitigate this.
Conclusions
Marked demographic disparities exist in the use of restrictive practice. Specific EIP care components may be associated with reductions. Strengthening evidence-based EIP provision and addressing structural inequalities may support progress towards less coercive and more equitable care.
Research suggests that well-developed parent engagement programs can boost early learning and reduce socioeconomic disparities in subsequent school adjustment. Yet few follow-up studies exist. To address this gap, we followed participants in the Research-based, Developmentally Informed-Parent [REDI-P] intervention study for 8 years to evaluate adolescent outcomes. Participants included 200 4-year-old children (55% White, 26% Black, 19% Latinx; 56% male, 44% female; Mage at study entry = 4.45 years) attending Head Start. Families were randomly assigned to REDI-P home learning materials and coaching or an attention control group. Multi-method measures tracked child literacy skills, learning behaviors, social competence, and conduct problems through grade 7. GLM analyses revealed significant preschool intervention effects on grade 7 working memory, β = 0.35, 95% CI 0.08, 0.62, p = .01; perceived social competence, β = 0.30, 95% CI 0.02, .58, p = .04; deviant peer affiliation, β = −0.33, 95% CI −0.60, −0.06, p = .02; and teacher-rated conduct problems, β = −0.30, 95% CI −0.58, −0.01, p = .04. Serial path models identified developmental progressions linking initial intervention effects to adolescent outcomes. Results highlight the long-term value of empowering parents to support the early social-emotional and pre-academic learning of their preschool children.
Infants with single ventricle CHD commonly experience gross motor delays due to physiological and environmental factors, including increased risk for white matter injury, reduced aerobic capacity, restrictive post-operative protocols, and limited movement opportunities. These delays persist in adolescence, affecting physical and social development. This study examines a quality improvement initiative within the National Pediatric Cardiology Quality Improvement Collaborative to enhance gross motor development.
Methods:
Fifteen centres participated. Gross motor skills were assessed using the Ages and Stages Questionnaires, Third Edition, at 6 and 12 months. A key driver diagram, Plan-Do-Study-Act cycles, baseline data, and ongoing process measures were collected. Interventions were implemented, including education, therapy support, and mobilisation protocols. Control charts were used to evaluate the data.
Results:
Scores from the Ages and Stages Questionnaires indicated delays in gross motor skills at baseline, with improvement over time. Participating centres showed a centerline shift from 41% to 89% of infants achieving on-target or improved motor scores, compared with 54% to 68% of infants at non-participating centres. Establishment of customised infant developmental plans increased from 62% to 74% for participating centres and from 53% to 61% for non-participating centres. Interventions included establishing processes for consistent screening, developmental plan administration, review of prone positioning, access to therapies, and early intervention referrals.
Conclusion:
This targeted quality improvement project increased the use of inpatient practices to support gross motor development for infants with single ventricle CHD. Collaborative, interdisciplinary efforts remain critical for addressing neurodevelopmental challenges in this high-risk population.
Individuals at clinical high risk (CHR) for psychosis exhibit both baseline and progressive brain structural abnormalities. However, the extent to which these changes reflect neurobiological trajectories of illness progression versus iatrogenic effects of antipsychotic (AP) treatment remains unresolved. A total of 148 AP-naïve CHRs and 65 healthy controls (HCs) underwent baseline structural magnetic resonance imaging (MRI) scans. One hundred thirty CHRs received second-generation AP treatment and completed 2-month follow-up scans. HCs also completed the follow-up scans. We compared baseline and longitudinal brain volume changes between CHRs and HCs and explored the relationship between AP treatment and brain structural changes in CHR. At baseline, CHRs showed enlarged third and inferior lateral ventricles compared to HCs. Within CHRs, larger ventricular, as well as smaller hippocampus and amygdala volumes, were associated with more severe symptoms and poorer functioning. No cortical volume differences were observed between groups at baseline, nor were cortical volumes related to clinical symptoms. After 2-month AP treatment, CHRs exhibited continued ventricular enlargement, reduced accumbens volume, and widespread cortical volume loss relative to HCs. Notably, cortical volume reductions were dose-dependent, with higher AP dose correlating with more pronounced cortical reductions. Additionally, cortical volume changes were linked to treatment response, with high-dose responders showing more significant HC-referenced changes compared to high-dose non-responders, low-dose responders, and low-dose non-responders. Our findings underscore the complex, region-specific, and clinically relevant neuroanatomical changes in CHR individuals, emphasizing the critical need to account for AP exposure in CHR neuroimaging studies.
This systematic review evaluates specialized psychosocial and complex interventions for early bipolar disorder (BD), early borderline personality disorder (BPD), early depression, early psychosis, and first-episode mental illness in general (FEMI).
Methods
We included systematic reviews and randomized controlled trials (RCTs) of interventions with psychosocial components, excluding trials that focused on pharmacological-only interventions and stand-alone psychotherapies. Searches were conducted in January 2023 across five databases. Review quality was assessed using AMSTAR-2 and risk of bias for RCTs using the Cochrane tool.
Results
Ten studies met the inclusion criteria: seven reviews and three RCTs. High-to moderate-quality evidence supports complex psychosocial interventions combined with pharmacotherapy for early psychosis. The most robust effects were reductions in relapse and improvements in psychosocial functioning; additional benefits were observed for symptom burden, remission, treatment discontinuation, and hospital admissions. Benefits were most sustained in longer-duration, community-based programs. For early BD, limited evidence suggests that combining pharmacotherapy with family-focused therapy or structured psychoeducation may improve the course of illness and treatment satisfaction. One RCT in early BPD reported improved engagement with a developmentally tailored program. Two FEMI RCTs found that nurse-led psychoeducation and psychosocial programs improved in-patient duration, symptoms, insight, self-efficacy, quality of life, and engagement. No eligible studies addressed early-stage depression, indicating a notable evidence gap for multimodal psychosocial interventions.
Conclusions
Complex psychosocial interventions are strongly supported for early psychosis. Preliminary data in BD, BPD, and FEMI suggest consistent benefits for engagement, but further rigorous trials – especially in early depression – focusing on different outcomes – are required.