Tilbage til forskningsbiblioteket
Original publikation
Udvidelse af koordineret specialiseret behandling til tidlig bipolar lidelse: Udvikling og implementering af STRIDE-modellen
Artiklen beskriver udviklingen og implementeringen af STRIDE-modellen, som er en tilpasset udgave af NAVIGATE-modellen for koordineret specialiseret behandling. Modellen er rettet mod tidlig bipolar lidelse og bygger på principperne fra den gældende standardbehandling for skizofrenispektrede lidelser.
Titel og resumé er skrevet på dansk med AI ud fra den originale publikation. Originalteksten står nedenfor.
Miley K, Coudray C, Bond D, Meyer-Kalos P. · Early intervention in psychiatry · 2026
AI-billedeCC BY 4.0 · © 2026 The Author(s). Early Intervention in Psychiatry published by John Wiley & Sons Australia, Ltd.
Teksten oversættes automatisk og kan indeholde fejl. Originalteksten på engelsk er den gældende. Oversættelsen er ikke medicinsk rådgivning.
Expanding Coordinated Specialty Care to Early‐Stage Bipolar Disorder: Development and Implementation of the STRIDE Model
Original dokumenttekst
ABSTRACT
Background
Coordinated specialty care (CSC) is the gold‐standard early intervention model for schizophrenia‐spectrum disorders. Similar models for bipolar disorder (BD) are lacking. This paper describes the development and implementation of STRIDE, an adaptation of the NAVIGATE CSC model for early‐stage BD.
Methods
Adaptations were developed based on literature review, international expert consultation and engagement with patient, family and clinician advisory groups. STRIDE was designed to be integrated with schizophrenia‐spectrum CSC services to build on existing expertise and infrastructure. Demographic and clinical data were collected at enrollment to characterise an initial STRIDE cohort of 19 participants between October 2023–June 2025.
Results
A detailed model of CSC for BD was developed and implemented. Many components of NAVIGATE, including a recovery focus, shared decision making and the coordinated services of individual psychotherapy, medication management, family psychoeducation and supported education and employment were maintained. Key adaptations for BD included modification of individual psychotherapy modules to address prevention and treatment of mood episodes, addition of modules on circadian and social rhythms, affect regulation and managing common psychiatric comorbidities, development of an early‐stage BD prescriber's manual and tailored family psychoeducation. Of 19 patients in the STRIDE cohort (mean age 25 years, 52.6% female), 89.5% were diagnosed with bipolar 1 disorder and 94.7% had a history of psychosis. Anxiety, depression, functional impairment and sleep disturbances were commonly reported at baseline.
Conclusions
STRIDE is a comprehensive adaptation of CSC for early‐stage BD. Further work is needed to assess STRIDE's feasibility, acceptability and effectiveness.
1 Introduction
Bipolar disorder (BD) is a common and disabling mood disorder which affects at least 37 million people worldwide (Ferrari et al. 2024). BD is the 4th leading cause of disability in young people (GBD 2019 Mental Disorders Collaborators 2022), driven by recurrent episodes of depression and mania/hypomania, which have devastating impacts on functioning and place patients at high risk for suicide (Plans et al. 2019; Simon et al. 2007). Clinical staging models conceptualise BD as a progressive condition beginning with an asymptomatic phase (stage 0), progressing to a first episode of threshold mood symptoms (stage 2) and for some individuals, multiple relapses and treatment resistance (stage 4) (Berk et al. 2007; Kapczinski et al. 2014). In line with the staging model, early diagnosis and treatment of BD are needed to prevent it from becoming more severe and disabling (Berk et al. 2010; Kozicky et al. 2016; Ratheesh et al. 2023; Swann et al. 1999). Some evidence suggests that pharmacological and behavioural treatments have greater efficacy when started early in the illness (Ratheesh et al. 2023), pointing to a potential critical period of intervention, consistent with the critical period hypothesis of psychosis (Birchwood et al. 1998). However, significant treatment delays exist, averaging up to 6–10 years and are associated with more time in mood episodes, psychiatric hospitalizations, self‐harm and functional decline (Buoli et al. 2021; Scott et al. 2022).
Young individuals with early‐stage BD have many treatment needs that must be addressed to achieve symptomatic and functional recovery. The onset of BD in the late adolescent to young adult years interrupts important developmental milestones such as accomplishing work, school and relationship goals (Coello et al. 2024; Sletved et al. 2022). Following an initial diagnosis of BD, relapse rates into mood episodes in those receiving medication treatment are 40% at 1 year and 60% at 4 years (Gignac et al. 2015b). Even after recovery from mood episodes, subthreshold mood symptoms and comorbid psychiatric conditions like anxiety disorders and ADHD are common and further impair functioning (Marangell et al. 2009; Perlis et al. 2006; Sentissi et al. 2008; Spoorthy et al. 2019; Tohen et al. 2003). Many other factors, such as developing psychological and behavioural symptom management strategies, avoiding substance use, regulating sleep, managing comorbid medical conditions and developing a support network are needed to help individuals with BD stay well and meet their life goals (Burdick et al. 2022; Gimenez‐Palomo et al. 2024).
Comprehensive BD early intervention programs to ensure early, accurate diagnoses and meet all of these needs are critically important to promote sustained recovery but are scarce. There is no defined standard of care for early‐stage BD and treatment guidelines are lacking (Chia et al. 2019). While some novel multidisciplinary early intervention programs for BD are emerging (Kessing et al. 2013; Ratheesh et al. 2025), most individuals are likely to receive treatment from fragmented clinical services in community settings from clinicians who are not specialists in BD. In contrast, a large evidence base has established coordinated specialty care (CSC) as the gold standard for individuals experiencing early‐stage schizophrenia spectrum disorders (SSDs) (Fusar‐Poli et al. 2017). CSC programs typically include up to 2 years of multidisciplinary services and have been shown to improve treatment engagement, psychiatric symptoms, hospitalisation rates, work and school participation and quality of life compared to usual care (Correll et al. 2018; Kane et al. 2016). NAVIGATE is a CSC model that was studied in the Recovery After an Initial Episode of Schizophrenia (RAISE) trial. NAVIGATE includes recovery‐focused psychotherapy, medication management, family education and school and education supports (Kane et al. 2016; Mueser, Penn, et al. 2015). RAISE demonstrated the effectiveness and feasibility of CSC in the United States health care landscape (Dixon et al. 2015; Kane et al. 2016), leading to the extensive implementation of schizophrenia‐spectrum CSC programs nationally (George et al. 2022).
There is an untapped opportunity to leverage the evidence base and infrastructure of schizophrenia‐spectrum CSC to develop and rapidly scale early intervention for BD. BD and SSDs are first diagnosed in young people and lead to many of the same developmental challenges and treatment needs. Yet, critical adaptations to schizophrenia‐spectrum CSC models are needed to address the unique clinical and functional needs of early‐stage BD. We developed STRIDE, an adaptation of the NAVIGATE CSC model, extensively tailored to early‐stage BD. STRIDE was designed to be integrated into existing early‐stage schizophrenia‐spectrum CSC teams to extend the reach of these services to those with BD. The purpose of this paper is to describe the development and intervention components of STRIDE, its initial clinical implementation and baseline characteristics and clinical profiles of the first cohort of enrolled patients. The feasibility, acceptability and preliminary outcomes of STRIDE will be described in a future report.
2 Methods
2.1 Intervention Development
STRIDE was developed by a team of investigators with expertise in early‐stage BD (DJB, KMM) and the NAVIGATE model for SSDs (PSM‐K, KMM) between November 2021 and June 2023. The Minnesota Department of Human Services funded its development due to a recognised need for early intervention in BD and to expand the capacity of NAVIGATE teams to better serve rural communities with a lower census of individuals with SSDs. We first brainstormed key needs of people with early‐stage BD that were not met by the existing NAVIGATE intervention, informed by extensive literature review. We then selected a group of internationally recognised experts in BD (N = 16) to provide feedback on the new or modified intervention components. To ensure STRIDE addressed all domains important to people living with BD and their families, we conducted 10 meetings with a patient advisory board of five BD patients and two meetings with family members and community clinicians. International experts with specific domain expertise worked with us to finalize the intervention components of STRIDE. Patients, family and community clinicians reviewed and contributed to select content areas included in the individual therapy and family psychoeducation modules, including a general overview of the STRIDE model and treatment components and specific feedback on intervention content spanning health and wellness, peer support, dialectical behaviour therapy (DBT), wellness planning and substance use. Patient and family advisors also contributed personal stories to be used in therapy modules focused on processing the first episode(s) for mania. STRIDE was so named by the patient advisory board to represent ‘hitting your stride’ and thriving with BD.
2.2 Target Population and Setting
STRIDE is designed for individuals aged 15–40 years who have received no more than 1 year of treatment for BD. The age range was chosen to align with the NAVIGATE inclusion criteria (Kane et al. 2016) and broadly captures the typical age of onset for bipolar spectrum disorders (Baldessarini et al. 2010; Bolton et al. 2021). It was developed to treat the entire range of bipolar‐spectrum disorders, including bipolar 1, bipolar 2 and other specified BD, with or without a history of psychosis. The program is intended to be implemented within existing NAVIGATE CSC teams in community settings. Integrating STRIDE within NAVIGATE CSC programs allows teams to build on existing expertise in providing recovery‐centred, team‐based care to young individuals with SMIs and leverages the existing infrastructure that supports team‐based care. Furthermore, the underlying diagnosis at enrollment into CSC is often not definitive. In situations where the diagnosis is not clear, decisions can be made about whether a patient should start with STRIDE or standard NAVIGATE based on team, patient and family consensus. Integration of STRIDE within a CSC program facilitates coordination or transition of care between STRIDE and NAVIGATE to best align with evolving clinical presentations. Like NAVIGATE, individuals may initiate services with STRIDE via referral from community clinicians, inpatient facilities or by self‐referral.
2.3 Clinical Program: Baseline Characteristics and Symptom Profiles
To assess the preliminary feasibility of extending NAVIGATE services to early‐stage BD, STRIDE was implemented as a pilot program in October 2023 at the University of Minnesota outpatient psychiatry clinic in a NAVIGATE‐informed CSC service. Demographic and clinical data were collected at enrollment from clinical interviews and electronic health records. Additional self‐report measures were completed via participation in the University of Minnesota's Early Psychosis Intervention Network (EPINET) study, EPI‐MINN. Self‐report measures included (1) the 10‐item Drug Abuse Screening Test (DAST‐10) (Skinner 1982), (2) the 3‐item Alcohol Use Disorders Identification Test (AUDIT‐C) (Barbor et al. 1992), (3) the 8‐item Patient Reported Outcomes Measures Information System (PROMIS) sleep disturbance short form (Yu et al. 2012) and (4) the Minnesota Symptom Severity Scale, which assesses the presence of a range of psychiatric symptoms and functional needs rated on a 0 (absent, not at all) to 4 (severe, nearly every day) scale. The University of Minnesota Institutional Review Board approved the implementation of STRIDE under a quality improvement designation and approved all EPI‐MINN activities. Patients enrolled in EPI‐MINN provided authorization to use their clinically‐obtained data for research purposes using an IRB‐approved form. Descriptive statistics were used to characterise the initial cohort of STRIDE participants who enrolled between October 2023–June 2025.
3 Results
3.1 Intervention Description
As with NAVIGATE, three conceptual frameworks, which are relevant to both young individuals with BD and SSDs, guided the development of STRIDE: the recovery model, the stress‐vulnerability model and psychiatric rehabilitation (Mueser, Gottlieb, et al. 2015). STRIDE is tailored to the unique needs and developmental stage of adolescents and young adults with BD. Treatment is aligned with goals related to individuation in relationships, vocational or educational pursuits, fostering self‐management of symptoms based on understanding the illness and individual risk and resiliency factors and facilitating self‐determination to counter the psychological impacts of living with a chronic illness (Mueser, Penn, et al. 2015).
Individuals with SSDs and early‐stage BD share many clinical characteristics already addressed by NAVIGATE, including high risk for problematic substance use (Duffy et al. 2014; Goldstein et al. 2013), suicidality (Simon et al. 2007) and decline in social and occupational functioning (Gignac et al. 2015a; Tohen et al. 2003). These components of NAVIGATE required no or limited adaptations for STRIDE. For example, the STRIDE Prescriber's Manual, like the NAVIGATE Prescriber's Manual (Robinson et al. 2018), emphasises shared decision‐making, improving adherence, ensuring medication tolerability and mitigating long‐term health risks and closely integrating with other team members and supports. STRIDE individual therapy maintains NAVIGATE's focus on psychoeducation, increasing resiliency and meeting personal goals, increasing natural supports and evidence‐based therapeutic skills such as cognitive‐behavioural therapy (Mueser, Penn, et al. 2015). Supported Employment and Education (SEE) services is a key NAVIGATE intervention that is transdiagnostic and was not modified for STRIDE (Mueser, Penn, et al. 2015).
However, STRIDE incorporates several key differences that are critical for recovery in BD (Tables 1 and 2). BD and SSD have different primary symptoms, different rates of comorbidities and distinct drivers of functional impairment. BD is predominantly a mood disorder and threshold and subthreshold mood symptoms, particularly depression and comorbid psychiatric illnesses like anxiety disorders and ADHD are the primary drivers of functional impairment (Burdick et al. 2022). In contrast, positive symptoms, negative symptoms and cognitive impairments predominate and drive poor functioning in SSDs (Santesteban‐Echarri et al. 2017). To address these differences, medication management, psychoeducation and therapeutic skills in STRIDE extend to managing the full range of symptoms in BD (depression, (hypo)mania, mixed episodes, subthreshold mood symptoms), addressing common negative schemas specific to BD (Ball et al. 2003; Macneil 2009), the addition of DBT skills with evidence for improving emotion regulation and addressing suicidality in BD (Goldstein et al. 2024; Jones et al. 2023), an emphasis on stabilising circadian and social rhythms (Frank et al. 1994; Goldstein et al. 2014; Hlastala et al. 2010; Inder et al. 2015) and management of key psychiatric comorbidities including anxiety, posttraumatic stress symptoms and ADHD (Léda‐Rêgo et al. 2024).
3.2 STRIDE Treatment Team and Intervention Components
In line with NAVIGATE (Kane et al. 2016), STRIDE includes four core interventions delivered by a coordinated team of clinicians with training in early‐stage BD: personalised medication management guided by the STRIDE Prescriber's Manual, resilience‐focused individual therapy (Increasing Resiliency in Life; IRL), family psychoeducation and SEE services. Two additional recommended intervention components have been added: peer support and health promotion. A program director coordinates referrals and services and all clinicians meet weekly for individual treatment planning. By extending CSC to early‐stage BD, teams can better utilise their clinician resources, especially in rural areas with lower rates of SSDs and BD (Powell et al. 2021). For this pilot, existing CSC clinicians were utilised without adding additional staff time. While there is expected variation in staffing needs based on regional population characteristics and catchment area size, we describe estimated staffing needs for teams in the Supporting Information. Initial length of treatment for STRIDE is conceptualised as up to 3 years to allow treatment flexibility based on individual remission and recurrence patterns.
3.2.1 Personalised Medication Management
STRIDE patients have frequent visits with a prescriber with training in the pharmacotherapy of early‐stage BD. The STRIDE Prescriber's Manual provides evidence‐based and expert‐informed guidance on pharmacotherapy for bipolar depression, mania, mixed states, maintenance treatment, common psychiatric comorbidities, side effect management, principles of health promotion and reproductive considerations. Due to the diagnostic instability of early‐stage BD patients, we also included a brief section on the pharmacological treatment of major depressive disorder with psychotic features. Initial medication doses and titration schedules are tailored to early‐stage patients. Principles of shared decision‐making (Farkas 2007; Towle et al. 1999) are followed and there is an emphasis on evidence‐based medications for BD, especially lithium (Ketter et al. 2006; Ratheesh et al. 2023; Swann et al. 1999; Yatham et al. 2018).
3.2.2 Increasing Resiliency in Life (IRL)
IRL is a manualized individual therapy that supports patients in recovery goals, provides education about BD and its treatment, promotes resiliency, improves self‐management and helps patients develop tools to prevent and manage symptoms. Following the NAVIGATE model, IRL is a recovery‐oriented psychotherapy rooted in cognitive behavioural therapy, illness management and recovery and motivational enhancement (Mueser, Penn, et al. 2015). It comprises 16 skills‐focused modules spanning BD symptom management, stress and resiliency, healthy lifestyles, relapse prevention and planning, processing mood episodes, DBT skills for BD, addressing symptoms and problems associated with trauma, decreasing substance use, stabilising circadian and social rhythms and improving interpersonal skills. STRIDE IRL clinicians receive training in these evidence‐based treatments and tailor the duration or depth of each module to individuals' specific needs. Some content areas are integrated throughout several IRL manuals. For example, content on stabilising circadian and social rhythms is included in the modules on managing stress and building resiliency, healthy lifestyles, cognitive approaches to sleep and coping with sleep problems (see Table 2 and the Supporting Information for further IRL module descriptions). The typical duration is 6–12 months. IRL is delivered by masters‐level clinicians.
3.2.3 Family Support & Education
STRIDE family supports aim to establish collaborative relationships between patients, their families and the treatment team, teach family members about BD and equip families with skills to assist their loved ones with their goals. Family education includes a 10–12 session curriculum covering BD symptoms, treatment and course; relapse prevention planning with family and patient; developing family resiliency; problem solving and communication strategies; and stress reduction skills. Family education is typically provided by the program director, a masters‐level clinician (Mueser, Penn, et al. 2015).
3.2.4 Supported Education and Employment (SEE)
The goal of SEE is to assist patients in achieving their educational and employment goals. A SEE specialist, typically a bachelor's‐level clinician, engages the patient in goal setting and provides practical assistance in job and educational program searching, obtaining work‐ and school‐related accommodations and identifying strategies to improve work and school performance (Mueser, Penn, et al. 2015; Rosenheck et al. 2017).
3.2.5 Additional Recommended Interventions
In addition to the standard NAVIGATE interventions, we recommend that STRIDE CSC teams include a peer support specialist who can meet individually with STRIDE patients. Peer support specialists can improve engagement, benefit recovery outcomes, reduce crisis service and inpatient admissions and increase self‐efficacy in people with SMIs (Fuhr et al. 2014; King and Simmons 2018; White et al. 2020). The peer specialist provides STRIDE patients with supports grounded in their own recovery journey and provides a valuable perspective to the treatment team. To address cardiometabolic health disparities faced by young individuals with BD (Chan et al. 2022; Miley et al. 2023), STRIDE includes a health promotion intervention which extends the health promotion content in the Prescriber's Guide and IRL therapy. It includes (1) a health promotion group curriculum drawn from evidence‐based interventions for BD with a focus on behaviour change and motivation enhancement for increasing physical activity and improving nutrition (Green et al. 2015; Sylvia 2015; Yarborough et al. 2016) and (2) recommendations for individual health coaching delivered by a registered nurse or health coach and individually tailored to assist patients with goal setting, treatment planning, accountability of lifestyle modifications and liaising with clinicians.
3.3 STRIDE Team Training
NAVIGATE clinicians receive extensive training in engaging and treating individuals with SSDs. To extend this expertise to early‐stage BD, additional training in BD assessment, course and treatment is needed. Recommended training includes an overview for all team members on the bipolar prodrome, pathways to care in BD, challenges to engagement in treatment and diagnostic considerations (including differential assessment between BD and non‐affective psychotic disorders and assessment of psychiatric comorbidities using recommended assessment scales provided in the program manual; see Supporting Information for more detail). To foster engagement of diverse populations, STRIDE includes an updated Assessment and Initial Goal setting module which includes questions to elicit information about individuals' background, race, ethnicity and cultural experiences and how they may or may not interact with illness. This assessment is intended to support the provision of culturally competent care, foster treatment alliance and reduce disengagement (Powell et al. 2021). Individual therapists, family clinicians and program directors attend a subsequent training providing an overview of BD education and treatment approaches in the IRL and family education manuals. Medication training for BD is divided into two sessions. The first training is attended by all team members and provides an overview of medications used to treat BD, common side effects, assessment and treatment of common psychiatric comorbidities and strategies to improve health monitoring and health promotion. Prescribers attend an additional training that provides a more detailed overview of the recommended medication guidelines. Following the training, two consultation call groups are provided, one for all team members and one for prescribers and team leaders, to discuss and problem‐solve any challenges.
3.4 Baseline Characteristics and Self‐Reported Measures
Nineteen patients enrolled in STRIDE between October 2023–June 2025 and provided authorization and consent for data collection. STRIDE patients had a mean age of 25 years and 52.6% identified as female (Table 3). At enrollment, 89.5% of patients were diagnosed with bipolar 1 disorder and 10.5% were diagnosed with bipolar 2 disorder or other BD. The most common mood state at enrollment was depressed (57.9%) (mean PHQ‐9 score 7.6 (SD 3.9)), with the remaining patients euthymic. Most patients (94.7%) had a history of psychosis. The mean number of medications prescribed was 2.5 (1.2), with 42.1% of patients prescribed 3 or more medications. 68.4% of patients were working or in school. The majority (73.7%) reported symptoms of at least one psychiatric comorbidity or substance use problem. Problematic drug use was self‐reported by 41.1% of patients, while 11.8% reported problematic alcohol use. Common self‐reported symptoms included anxiety (64.7%), depression (64.7%), difficulty functioning at work or school (58.8%) and sleep disturbance (41.2%). No patients reported current psychosis symptoms at enrollment.
4 Discussion
In this report, we describe STRIDE, an adaptation of NAVIGATE CSC (Kane et al. 2016) for early‐stage BD and the baseline characteristics of the initial cohort of STRIDE patients. Our initial implementation and enrollment data show that patients with early‐stage BD will seek care in CSC programs. Our assessment of baseline characteristics of the initial STRIDE cohort suggests that the intervention components are aligned with identified clinical domains. Further evaluation of the feasibility, acceptability and effectiveness of STRIDE is needed.
STRIDE demonstrates that the NAVIGATE CSC model for SSD can be adapted for people with early‐stage BD. Several CSC intervention components and treatment tenets—including a focus on recovery and shared decision‐making, along with SEE services—are transdiagnostic and require little modification. Other intervention components required significant adaptations to adequately target the treatment needs of young individuals with BD. Key modifications addressed the full range of mood symptoms in BD (depression, (hypo)mania, mixed episodes), inter‐episode emotion regulation, negative schemas, suicidality and comorbidities including anxiety, PTSD, ADHD and circadian rhythm disturbances. Due to the extensive differences in prescribing for SSDs and BD (Robinson et al. 2018; Yatham et al. 2018), the STRIDE Prescriber's Manual was created anew, although a focus on shared decision‐making, promoting adherence and enhancing tolerability of medications was maintained.
Consistent with research in first‐episode mania cohorts (Gignac et al. 2015b), we identified many potential treatment needs in our early‐stage BD cohort. At enrollment, STRIDE patients tended to have threshold or subthreshold depression symptoms. A large portion had psychiatric or substance use comorbidities and polypharmacy was common. The most common self‐reported symptoms were depression, anxiety, sleep disturbances and impairment in psychosocial functioning. While STRIDE intervention components address each of these areas, longitudinal evaluation will be needed to understand how well STRIDE leads to improvements in symptoms and functioning.
Few evidence‐based, multidisciplinary early intervention programs for BD exist. Kessing et al. (2013) found that 2 years of care in a specialised mood disorder clinic in Denmark, including evidence‐based pharmacologic treatment and group psychoeducation, led to reduced hospitalizations, increased use of mood stabilisers and increased care satisfaction compared to treatment as usual. Analysis of outcomes at a 16‐year follow‐up suggested promising long‐term effects on suicidality and found that the intervention was associated with fewer (but not statistically significant) psychiatric admissions, lower costs and increased use of lithium and antipsychotics (Munkholm and Kessing 2024). Ratheesh et al. (2025) developed BLEND, a 6‐month early intervention program with components of guideline‐concordant pharmacotherapy, a blended in‐person individual therapy combined with digital therapeutic content and digital relapse monitoring. In a sample of 21 young people, BLEND was found to be feasible, acceptable and led to improvements in suicidality. STRIDE contains similar components to these models, but the specific team structure and integration with schizophrenia‐spectrum CSC distinguish STRIDE from existing early‐intervention models. Although digital interventions are an emerging area for early intervention, they are not yet standard of care in most CSC programs and incorporation of a digital component for STRIDE was not feasible during initial intervention development.
STRIDE was designed to be integrated with SSD CSC programs to leverage existing resources and clinical expertise in treating early‐stage SMIs. As such, it can be readily deployed and scaled as an extension of the more than 350 CSC programs in the United States, of which NAVIGATE is the most common treatment model (Kazandjian et al. 2022). However, integrating STRIDE with SSD CSC services may also present some challenges. First, it may be challenging to reach people experiencing BD without psychosis, as indicated by the high proportion of patients enrolled into STRIDE with a history of psychosis. The best way to reach people with BD without psychosis, including those with bipolar 2 disorder and other specified BDs, requires further study and may require active community outreach and engagement with existing mental health services. It is also unknown how the care pathways and service use of CSC interventions will differ among those with BD compared to SSDs (Phalen et al. 2025; Polillo et al. 2023). It is possible that the frequency of engagement and the length of care required to achieve recovery in BD differs from that in SSDs. For example, due to the episodic nature of mood episodes in BD, CSC for early‐stage BD may benefit from more flexible enrollment periods with the ability of patients to step up or down in service intensity or to return to services after discharge in the early illness phases, as needed. Additionally, functional impairments associated with early‐stage BD may differ compared to SSDs and may result in different SEE needs. Racial and socioeconomic disparities in access, engagement and outcomes associated with CSC have been identified (Bennett and Rosenheck 2021; Moe et al. 2024; van der Ven et al. 2022). In our initial STRIDE implementation, most enrolled patients were White and further efforts to understand how STRIDE can equitably reach those from diverse sociodemographic backgrounds are critical. There is currently no consensus definition of early‐stage BD and how to best operationalise this for clinical services like STRIDE remains an open question. Whether existing CSC teams have the capacity to extend their reach to those with BD is not completely understood. While equipping teams to treat early‐stage BD may enhance the sustainability of programs with lower census, such as those in rural areas, the demand for SSD CSC care is high and not fully met by current services in more populated areas (Kazandjian et al. 2022; Powell et al. 2021). The expansion of CSC to young individuals with BD will likely require support from healthcare funders to ensure access (Dixon 2017; George et al. 2022). We did not systematically collect STRIDE referral data to understand overall program demand and reach and such data would inform broader implementation feasibility. Finally, while CSC is the gold standard treatment model for first episode SSDs, it is unknown whether it is the optimal model for early‐stage BD and further research is needed to confirm whether the known benefits of CSC extend to those with early‐stage BD.
5 Conclusions
We developed and implemented STRIDE, an extension of the NAVIGATE CSC model for first episode SSDs tailored to early‐stage BD. By leveraging the extensive CSC infrastructure, STRIDE has the potential to be rapidly scaled in real‐world settings to fill a critical gap in early intervention for BD. Further research is needed to evaluate STRIDE's feasibility and effectiveness.
Funding
This work was supported by the Minnesota Department of Human Services.
Ethics Statement
The University of Minnesota Institutional Review Board approved implementation of STRIDE under a quality improvement designation and approved all EPI‐MINN study activities. Patients enrolled in EPI‐MINN provided authorization to use their clinically‐obtained data for research purposes using an IRB‐approved form. When a patient was under the age of 18, a parent or guardian co‐signed the authorization form; similarly, if the patient was an adult who had a legal guardian make medical decisions on their behalf, their guardian co‐signed. Analytic methods, study materials and data may be made available upon request to the corresponding author.
Conflicts of Interest
Piper Meyer‐Kalos, Kathleen Miley and David Bond provide training and consultation about implementing STRIDE that can include compensation.
Referencer citeret i publikationen
- Amerio, A. , D. Russo , N. Miletto , et al. 2021. “Polypharmacy as Maintenance Treatment in Bipolar Illness: A Systematic Review.” Acta Psychiatrica Scandinavica 144, no. 3: 259–276. 10.1111/acps.13312.33960396 PMC8453557
- Baldessarini, R. J. , L. Bolzani , N. Cruz , et al. 2010. “Onset‐Age of Bipolar Disorders at Six International Sites.” Journal of Affective Disorders 121, no. 1–2: 143–146. 10.1016/j.jad.2009.05.030.19560827
- Baldessarini, R. J. , and L. Tondo . 2000. “Does Lithium Treatment Still Work? Evidence of Stable Responses Over Three Decades.” Archives of General Psychiatry 57, no. 2: 187–190. 10.1001/archpsyc.57.2.187.10665622
- Ball, J. , P. Mitchell , G. Malhi , A. Skillecorn , and M. Smith . 2003. “Schema‐Focused Cognitive Therapy for Bipolar Disorder: Reducing Vulnerability to Relapse Through Attitudinal Change.” Australian and New Zealand Journal of Psychiatry 37, no. 1: 41–48. 10.1046/j.1440-1614.2003.01098.x.12534655
- Barbor, T. , J. De La Fuente , J. Saunders , and M. Grant . 1992. AUDIT: The Alcohol Use Disorders Identification Test: Guidelines for Use in Primary Health Care. World Health Organization.
- Bennett, D. , and R. Rosenheck . 2021. “Socioeconomic Status and the Effectiveness of Treatment for First‐Episode Psychosis.” Health Services Research 56, no. 3: 409–417. 10.1111/1475-6773.13606.33231881 PMC8143679
- Berk, M. , P. Conus , N. Lucas , et al. 2007. “Setting the Stage: From Prodrome to Treatment Resistance in Bipolar Disorder.” Bipolar Disorders 9, no. 7: 671–678. 10.1111/j.1399-5618.2007.00484.x.17988356
- Berk, M. , R. Daglas , O. Dandash , et al. 2017. “Quetiapine v. Lithium in the Maintenance Phase Following a First Episode of Mania: Randomised Controlled Trial.” British Journal of Psychiatry 210, no. 6: 413–421. 10.1192/bjp.bp.116.186833.28254958
- Berk, M. , K. Hallam , G. S. Malhi , et al. 2010. “Evidence and Implications for Early Intervention in Bipolar Disorder.” Journal of Mental Health 19, no. 2: 113–126. 10.3109/09638230903469111.20433320
- Birchwood, M. , P. Todd , and C. Jackson . 1998. “Early Intervention in Psychosis. The Critical Period Hypothesis.” British Journal of Psychiatry. Supplement 172, no. 33: 53–59.9764127
- Bolton, S. , J. Warner , E. Harriss , J. Geddes , and K. E. A. Saunders . 2021. “Bipolar Disorder: Trimodal Age‐At‐Onset Distribution.” Bipolar Disorders 23, no. 4: 341–356. 10.1111/bdi.13016.33030292 PMC8359178
- Buoli, M. , B. M. Cesana , A. Fagiolini , et al. 2021. “Which Factors Delay Treatment in Bipolar Disorder? A Nationwide Study Focussed on Duration of Untreated Illness.” Early Intervention in Psychiatry 15, no. 5: 1136–1145.33058435 10.1111/eip.13051
- Burdick, K. E. , C. E. Millett , A. K. Yocum , et al. 2022. “Predictors of Functional Impairment in Bipolar Disorder: Results From 13 Cohorts From Seven Countries by the Global Bipolar Cohort Collaborative.” Bipolar Disorders 24, no. 7: 709–719. 10.1111/bdi.13208.35322518 PMC9500115
- Chan, J. K. N. , C. H. Y. Tong , C. S. M. Wong , E. Y. H. Chen , and W. C. Chang . 2022. “Life Expectancy and Years of Potential Life Lost in Bipolar Disorder: Systematic Review and Meta‐Analysis.” British Journal of Psychiatry 221, no. 3: 567–576. 10.1192/bjp.2022.19.35184778
- Chen, P. H. , S. Y. Tsai , P. Y. Chen , et al. 2023. “Mood Stabilizers and Risk of All‐Cause, Natural, and Suicide Mortality in Bipolar Disorder: A Nationwide Cohort Study.” Acta Psychiatrica Scandinavica 147, no. 3: 234–247. 10.1111/acps.13519.36367926
- Chia, M. F. , S. Cotton , K. Filia , et al. 2019. “Early Intervention for Bipolar Disorder–Do Current Treatment Guidelines Provide Recommendations for the Early Stages of the Disorder?” Journal of Affective Disorders 257: 669–677.31377603 10.1016/j.jad.2019.07.062
- Coello, K. , C. Stanislaus , S. Stanislaus , et al. 2024. “Socio‐Economic Status, Functioning and Cognition in Young Versus Adult Patients Newly Diagnosed With Bipolar Disorder and Their Unaffected Relatives; Results From a Cross‐Sectional Study.” Journal of Affective Disorders 351: 458–471. 10.1016/j.jad.2024.01.174.38266931
- Correll, C. U. , B. Galling , A. Pawar , et al. 2018. “Comparison of Early Intervention Services vs Treatment as Usual for Early‐Phase Psychosis: A Systematic Review, Meta‐Analysis, and Meta‐Regression.” JAMA Psychiatry 75, no. 6: 555–565. 10.1001/jamapsychiatry.2018.0623.29800949 PMC6137532
- Deckersbach, T. , L. Eisner , and L. Sylvia . 2016. “Cognitive Behavioral Therapy for Bipolar Disorder.” In The Massachusetts General Hospital Handbook of Cognitive Behavioral Therapy, edited by T. Deckersbach , A. S. Bratiotis , S. E. Stewart , and G. Steketee , 87–103. Springer.
- DeCou, C. R. , K. A. Comtois , and S. J. Landes . 2019. “Dialectical Behavior Therapy Is Effective for the Treatment of Suicidal Behavior: A Meta‐Analysis.” Behavior Therapy 50, no. 1: 60–72.30661567 10.1016/j.beth.2018.03.009
- Dixon, L. 2017. “What It Will Take to Make Coordinated Specialty Care Available to Anyone Experiencing Early Schizophrenia: Getting Over the Hump.” JAMA Psychiatry 74, no. 1: 7–8. 10.1001/jamapsychiatry.2016.2665.27851843
- Dixon, L. , H. H. Goldman , M. E. Bennett , et al. 2015. “Implementing Coordinated Specialty Care for Early Psychosis: The RAISE Connection Program.” Psychiatric Services 66, no. 7: 691–698. 10.1176/appi.ps.201400281.25772764 PMC5637730
- Duffy, A. , J. Horrocks , S. Doucette , C. Keown‐Stoneman , S. McCloskey , and P. Grof . 2014. “The Developmental Trajectory of Bipolar Disorder.” British Journal of Psychiatry 204, no. 2: 122–128. 10.1192/bjp.bp.113.126706.24262817
- Farkas, M. 2007. “The Vision of Recovery Today: What It Is and What It Means for Services.” World Psychiatry 6, no. 2: 68–74.18235855 PMC2219905
- Ferrari, A. J. , D. F. Santomauro , A. Aali , et al. 2024. “Global Incidence, Prevalence, Years Lived With Disability (YLDs), Disability‐Adjusted Life‐Years (DALYs), and Healthy Life Expectancy (HALE) for 371 Diseases and Injuries in 204 Countries and Territories and 811 Subnational Locations, 1990–2021: A Systematic Analysis for the Global Burden of Disease Study 2021.” Lancet 403, no. 10440: 2133–2161.38642570 10.1016/S0140-6736(24)00757-8PMC11122111
- Frank, E. , D. Kupfer , C. Ehlers , and T. Monk . 1994. “Interpersonal and Social Rhythm Therapy for Bipolar Disorder: Integrating Interpersonal and Behavioral Approaches.” Behavior Therapist 17: 143–143.
- Frank, E. , H. Swartz , and D. Kupfer . 2019. “Interpersonal and Social Rhythm Therapy: Managing the Chaos of Bipolar Disorder.” In Bipolar Disorder: The Science of Mental Health, edited by S. E. Hyman , 257–268. Routledge.10.1016/s0006-3223(00)00969-011018230
- Fuhr, D. C. , T. T. Salisbury , M. J. De Silva , et al. 2014. “Effectiveness of Peer‐Delivered Interventions for Severe Mental Illness and Depression on Clinical and Psychosocial Outcomes: A Systematic Review and Meta‐Analysis.” Social Psychiatry and Psychiatric Epidemiology 49, no. 11: 1691–1702. 10.1007/s00127-014-0857-5.24632847 PMC4167169
- Fusar‐Poli, P. , P. D. McGorry , and J. M. Kane . 2017. “Improving Outcomes of First‐Episode Psychosis: An Overview.” World Psychiatry 16, no. 3: 251–265. 10.1002/wps.20446.28941089 PMC5608829
- GBD 2019 Mental Disorders Collaborators . 2022. “Global, Regional, and National Burden of 12 Mental Disorders in 204 Countries and Territories, 1990–2019: A Systematic Analysis for the Global Burden of Disease Study 2019.” Lancet Psychiatry 9, no. 2: 137–150.35026139 10.1016/S2215-0366(21)00395-3PMC8776563
- George, P. , S. S. Ghose , H. H. Goldman , et al. 2022. “Growth of Coordinated Specialty Care in the United States With Changes in Federal Funding Policies: 2014‐2018.” Psychiatric Services 73, no. 12: 1346–1351. 10.1176/appi.ps.202100600.35707858 PMC9722492
- Gignac, A. , A. McGirr , R. W. Lam , and L. N. Yatham . 2015a. “Course and Outcome Following a First Episode of Mania: Four‐Year Prospective Data From the Systematic Treatment Optimization Program (STOP‐EM).” Journal of Affective Disorders 175: 411–417. 10.1016/j.jad.2015.01.032.25678174
- Gignac, A. , A. McGirr , R. W. Lam , and L. N. Yatham . 2015b. “Recovery and Recurrence Following a First Episode of Mania: A Systematic Review and Meta‐Analysis of Prospectively Characterized Cohorts.” Journal of Clinical Psychiatry 76, no. 9: 1241–1248. 10.4088/JCP.14r09245.25845021
- Gimenez‐Palomo, A. , H. Andreu , L. Olivier , et al. 2024. “Clinical, Sociodemographic and Environmental Predicting Factors for Relapse in Bipolar Disorder: A Systematic Review.” Journal of Affective Disorders 360: 276–296. 10.1016/j.jad.2024.05.064.38797389
- Goldstein, B. I. , M. Strober , D. Axelson , et al. 2013. “Predictors of First‐Onset Substance Use Disorders During the Prospective Course of Bipolar Spectrum Disorders in Adolescents.” Journal of the American Academy of Child and Adolescent Psychiatry 52, no. 10: 1026–1037. 10.1016/j.jaac.2013.07.009.24074469 PMC3787940
- Goldstein, T. R. , R. Fersch‐Podrat , D. A. Axelson , et al. 2014. “Early Intervention for Adolescents at High Risk for the Development of Bipolar Disorder: Pilot Study of Interpersonal and Social Rhythm Therapy (IPSRT).” Psychotherapy (Chicago, Ill.) 51, no. 1: 180–189. 10.1037/a0034396.24377402
- Goldstein, T. R. , J. Merranko , N. Rode , et al. 2024. “Dialectical Behavior Therapy for Adolescents With Bipolar Disorder: A Randomized Clinical Trial.” JAMA Psychiatry 81, no. 1: 15–24. 10.1001/jamapsychiatry.2023.3399.37703037 PMC10500432
- Green, C. A. , B. J. Yarborough , M. C. Leo , et al. 2015. “The STRIDE Weight Loss and Lifestyle Intervention for Individuals Taking Antipsychotic Medications: A Randomized Trial.” American Journal of Psychiatry 172, no. 1: 71–81. 10.1176/appi.ajp.2014.14020173.25219423 PMC4282602
- Hafeman, D. M. , K. D. Chang , A. S. Garrett , E. M. Sanders , and M. L. Phillips . 2012. “Effects of Medication on Neuroimaging Findings in Bipolar Disorder: An Updated Review.” Bipolar Disorders 14, no. 4: 375–410. 10.1111/j.1399-5618.2012.01023.x.22631621
- Harvey, A. G. , A. M. Soehner , K. A. Kaplan , et al. 2015. “Treating Insomnia Improves Mood State, Sleep, and Functioning in Bipolar Disorder: A Pilot Randomized Controlled Trial.” Journal of Consulting and Clinical Psychology 83, no. 3: 564–577. 10.1037/a0038655.25622197 PMC4446240
- Hlastala, S. A. , J. S. Kotler , J. M. McClellan , and E. A. McCauley . 2010. “Interpersonal and Social Rhythm Therapy for Adolescents With Bipolar Disorder: Treatment Development and Results From an Open Trial.” Depression and Anxiety 27, no. 5: 457–464. 10.1002/da.20668.20186968 PMC4318681
- Inder, M. L. , M. T. Crowe , S. E. Luty , et al. 2015. “Randomized, Controlled Trial of Interpersonal and Social Rhythm Therapy for Young People With Bipolar Disorder.” Bipolar Disorders 17, no. 2: 128–138. 10.1111/bdi.12273.25346391
- Jones, B. D. M. , M. Umer , M. E. Kittur , et al. 2023. “A Systematic Review on the Effectiveness of Dialectical Behavior Therapy for Improving Mood Symptoms in Bipolar Disorders.” International Journal of Bipolar Disorders 11, no. 1: 6. 10.1186/s40345-023-00288-6.36739574 PMC9899872
- Kane, J. M. , D. G. Robinson , N. R. Schooler , et al. 2016. “Comprehensive Versus Usual Community Care for First‐Episode Psychosis: 2‐Year Outcomes From the NIMH RAISE Early Treatment Program.” American Journal of Psychiatry 173, no. 4: 362–372. 10.1176/appi.ajp.2015.15050632.26481174 PMC4981493
- Kapczinski, F. , P. V. Magalhaes , V. Balanza‐Martinez , et al. 2014. “Staging Systems in Bipolar Disorder: An International Society for Bipolar Disorders Task Force Report.” Acta Psychiatrica Scandinavica 130, no. 5: 354–363. 10.1111/acps.12305.24961757
- Kazandjian, M. , K. Neylon , S. Ghose , et al. 2022. State Snapshot 2021–2022: Early Psychosis Programming Across the United States. https://nationalepinet.org/.
- Keepers, G. A. , L. J. Fochtmann , J. M. Anzia , et al. 2020. “The American Psychiatric Association Practice Guideline for the Treatment of Patients With Schizophrenia.” American Journal of Psychiatry 177, no. 9: 868–872.32867516 10.1176/appi.ajp.2020.177901
- Kessing, L. V. , H. V. Hansen , A. Hvenegaard , et al. 2013. “Treatment in a Specialised Out‐Patient Mood Disorder Clinic v. Standard Out‐Patient Treatment in the Early Course of Bipolar Disorder: Randomised Clinical Trial.” British Journal of Psychiatry 202, no. 3: 212–219. 10.1192/bjp.bp.112.113548.23349295
- Ketter, T. A. , J. P. Houston , D. H. Adams , et al. 2006. “Differential Efficacy of Olanzapine and Lithium in Preventing Manic or Mixed Recurrence in Patients With Bipolar I Disorder Based on Number of Previous Manic or Mixed Episodes.” Journal of Clinical Psychiatry 67, no. 1: 95–101. 10.4088/jcp.v67n0113.16426094
- King, A. J. , and M. B. Simmons . 2018. “A Systematic Review of the Attributes and Outcomes of Peer Work and Guidelines for Reporting Studies of Peer Interventions.” Psychiatric Services 69, no. 9: 961–977. 10.1176/appi.ps.201700564.29962310
- Kothgassner, O. D. , A. Goreis , K. Robinson , M. M. Huscsava , C. Schmahl , and P. L. Plener . 2021. “Efficacy of Dialectical Behavior Therapy for Adolescent Self‐Harm and Suicidal Ideation: A Systematic Review and Meta‐Analysis.” Psychological Medicine 51, no. 7: 1057–1067. 10.1017/S0033291721001355.33875025 PMC8188531
- Kozicky, J. M. , A. McGirr , D. J. Bond , et al. 2016. “Neuroprogression and Episode Recurrence in Bipolar I Disorder: A Study of Gray Matter Volume Changes in First‐Episode Mania and Association With Clinical Outcome.” Bipolar Disorders 18, no. 6: 511–519. 10.1111/bdi.12437.27759214
- Léda‐Rêgo, G. , P. Studart‐Bottó , P. Abbade , et al. 2024. “Lifetime Prevalence of Psychiatric Comorbidities in Patients With Bipolar Disorder: A Systematic Review and Meta‐Analysis.” Psychiatry Research 337: 115953. 10.1016/j.psychres.2024.115953.38763079
- Linehan, M. M. , K. A. Comtois , A. M. Murray , et al. 2006. “Two‐Year Randomized Controlled Trial and Follow‐Up of Dialectical Behavior Therapy vs Therapy by Experts for Suicidal Behaviors and Borderline Personality Disorder.” Archives of General Psychiatry 63, no. 7: 757–766. 10.1001/archpsyc.63.7.757.16818865
- Macneil, C. A. 2009. Bipolar Disorder in Young People: A Psychological Intervention Manual. Cambridge University Press.
- Malhi, G. S. , E. Bell , M. Jadidi , M. Gitlin , and M. Bauer . 2023. “Countering the Declining Use of Lithium Therapy: A Call to Arms.” International Journal Bipolar Disorders 11, no. 1: 30. 10.1186/s40345-023-00310-x.PMC1046032737633877
- Marangell, L. B. , E. B. Dennehy , S. Miyahara , et al. 2009. “The Functional Impact of Subsyndromal Depressive Symptoms in Bipolar Disorder: Data From STEP‐BD.” Journal of Affective Disorders 114, no. 1–3: 58–67. 10.1016/j.jad.2008.07.006.18708263 PMC2704060
- Melo, M. C. A. , R. L. C. Abreu , V. B. Linhares Neto , P. F. C. de Bruin , and V. M. S. de Bruin . 2017. “Chronotype and Circadian Rhythm in Bipolar Disorder: A Systematic Review.” Sleep Medicine Reviews 34: 46–58. 10.1016/j.smrv.2016.06.007.27524206
- Miley, K. M. , S. A. Hooker , A. L. Crain , et al. 2023. “30‐Year Cardiovascular Disease Risk for Young Adults With Serious Mental Illness.” General Hospital Psychiatry 85: 139–147. 10.1016/j.genhosppsych.2023.10.015.38487652 PMC10936711
- Moe, A. M. , E. Llamocca , H. M. Wastler , et al. 2024. “Racial and Ethnic Disparities in the Diagnosis and Early Treatment of First‐Episode Psychosis.” Schizophrenia Bulletin Open 5, no. 1: sgae019. 10.1093/schizbullopen/sgae019.39206276 PMC11350282
- Mueser, K. T. , J. D. Gottlieb , H. Xie , et al. 2015. “Evaluation of Cognitive Restructuring for Post‐Traumatic Stress Disorder in People With Severe Mental Illness.” British Journal of Psychiatry 206, no. 6: 501–508. 10.1192/bjp.bp.114.147926.PMC445021925858178
- Mueser, K. T. , D. L. Penn , J. Addington , et al. 2015. “The NAVIGATE Program for First‐Episode Psychosis: Rationale, Overview, and Description of Psychosocial Components.” Psychiatric Services 66, no. 7: 680–690. 10.1176/appi.ps.201400413.25772766 PMC4490051
- Munkholm, K. , and L. V. Kessing . 2024. “Early Specialised Treatment for Bipolar Disorder: Long‐Term Follow‐Up From the Early Intervention in Affective Disorders (EIA) Randomised Controlled Trial.” Acta Psychiatrica Scandinavica 150, no. 3: 138–147. 10.1111/acps.13716.38825333
- Murray, G. , M. Suto , R. Hole , S. Hale , E. Amari , and E. E. Michalak . 2011. “Self‐Management Strategies Used by 'high Functioning' Individuals With Bipolar Disorder: From Research to Clinical Practice.” Clinical Psychology & Psychotherapy 18, no. 2: 95–109. 10.1002/cpp.710.20572206
- Nishith, P. , K. T. Mueser , and G. A. Morse . 2015. “A Brief Intervention for Posttraumatic Stress Disorder in Persons With a Serious Mental Illness.” Psychiatric Rehabilitation Journal 38, no. 4: 314–319. 10.1037/prj0000158.26414747
- Otto, M. W. , C. A. Perlman , R. Wernicke , H. E. Reese , M. S. Bauer , and M. H. Pollack . 2004. “Posttraumatic Stress Disorder in Patients With Bipolar Disorder: A Review of Prevalence, Correlates, and Treatment Strategies.” Bipolar Disorders 6, no. 6: 470–479. 10.1111/j.1399-5618.2004.00151.x.15541062
- Ozdel, K. , A. Kart , and M. H. Turkcapar . 2021. “Cognitive Behavioral Therapy in Treatment of Bipolar Disorder.” Nöro Psikiyatri Arşivi 58, no. Suppl 1: S66–S76. 10.29399/npa.27419.34658638 PMC8498810
- Pavlova, B. , R. H. Perlis , M. Alda , and R. Uher . 2015. “Lifetime Prevalence of Anxiety Disorders in People With Bipolar Disorder: A Systematic Review and Meta‐Analysis.” Lancet Psychiatry 2, no. 8: 710–717. 10.1016/S2215-0366(15)00112-1.26249302
- Perlis, R. H. , M. J. Ostacher , J. K. Patel , et al. 2006. “Predictors of Recurrence in Bipolar Disorder: Primary Outcomes From the Systematic Treatment Enhancement Program for Bipolar Disorder (STEP‐BD).” American Journal of Psychiatry 163, no. 2: 217–224. 10.1176/appi.ajp.163.2.217.16449474
- Phalen, P. L. , W. R. Smith , N. Jones , et al. 2025. “Reasons for Discharge in a National Network of Early Psychosis Intervention Programs.” Schizophrenia Bulletin 51, no. 3: 722–729. 10.1093/schbul/sbae100.39030696 PMC12077663
- Plans, L. , C. Barrot , E. Nieto , et al. 2019. “Association Between Completed Suicide and Bipolar Disorder: A Systematic Review of the Literature.” Journal of Affective Disorders 242: 111–122. 10.1016/j.jad.2018.08.054.30173059
- Polillo, A. , G. Foussias , W. Wang , et al. 2023. “Care Pathways and Initial Engagement in Early Psychosis Intervention Services Among Youths and Young Adults.” JAMA Network Open 6, no. 9: e2333526. 10.1001/jamanetworkopen.2023.33526.37703014 PMC10500372
- Powell, A. L. , C. Hinger , E. D. Marshall‐Lee , T. Miller‐Roberts , and K. Phillips . 2021. “Implementing Coordinated Specialty Care for First Episode Psychosis: A Review of Barriers and Solutions.” Community Mental Health Journal 57, no. 2: 268–276. 10.1007/s10597-020-00644-1.32472286
- Ratheesh, A. , J. Gates , D. Hammond , et al. 2025. “Bipolar Early Intervention Using New Digital Technologies (BLEND): A Pilot Randomised Controlled Trial of a Novel Blended‐Digital Early Intervention Model of Care for Youth With Bipolar Disorder I or II.” Early Intervention in Psychiatry 19, no. 6: e70060. 10.1111/eip.70060.40539376 PMC12179817
- Ratheesh, A. , D. Hett , J. Ramain , et al. 2023. “A Systematic Review of Interventions in the Early Course of Bipolar Disorder I or II: A Report of the International Society for Bipolar Disorders Taskforce on Early Intervention.” International Journal of Bipolar Disorders 11, no. 1: 1. 10.1186/s40345-022-00275-3.36595095 PMC9810772
- Robinson, D. G. , N. R. Schooler , C. U. Correll , et al. 2018. “Psychopharmacological Treatment in the RAISE‐ETP Study: Outcomes of a Manual and Computer Decision Support System Based Intervention.” American Journal of Psychiatry 175, no. 2: 169–179. 10.1176/appi.ajp.2017.16080919.28945118 PMC5794655
- Rodrigues Cordeiro, C. , B. R. Corte‐Real , R. Saraiva , B. N. Frey , F. Kapczinski , and T. de Azevedo Cardoso . 2023. “Triggers for Acute Mood Episodes in Bipolar Disorder: A Systematic Review.” Journal of Psychiatric Research 161: 237–260. 10.1016/j.jpsychires.2023.03.008.36940629
- Rosenheck, R. , K. T. Mueser , K. Sint , et al. 2017. “Supported Employment and Education in Comprehensive, Integrated Care for First Episode Psychosis: Effects on Work, School, and Disability Income.” Schizophrenia Research 182: 120–128. 10.1016/j.schres.2016.09.024.27667369
- Sandstrom, A. , N. Perroud , M. Alda , R. Uher , and B. Pavlova . 2021. “Prevalence of Attention‐Deficit/Hyperactivity Disorder in People With Mood Disorders: A Systematic Review and Meta‐Analysis.” Acta Psychiatrica Scandinavica 143, no. 5: 380–391. 10.1111/acps.13283.33528847
- Santesteban‐Echarri, O. , M. Paino , S. Rice , et al. 2017. “Predictors of Functional Recovery in First‐Episode Psychosis: A Systematic Review and Meta‐Analysis of Longitudinal Studies.” Clinical Psychology Review 58: 59–75. 10.1016/j.cpr.2017.09.007.29042139
- Scott, J. , A. Graham , A. Yung , C. Morgan , F. Bellivier , and B. Etain . 2022. “A Systematic Review and Meta‐Analysis of Delayed Help‐Seeking, Delayed Diagnosis and Duration of Untreated Illness in Bipolar Disorders.” Acta Psychiatrica Scandinavica 146, no. 5: 389–405. 10.1111/acps.13490.36018259
- Sentissi, O. , J. C. Navarro , H. De Oliveira , et al. 2008. “Bipolar Disorders and Quality of Life: The Impact of Attention Deficit/Hyperactivity Disorder and Substance Abuse in Euthymic Patients.” Psychiatry Research 161, no. 1: 36–42. 10.1016/j.psychres.2007.06.016.18786727
- Simon, G. E. , E. Hunkeler , B. Fireman , J. Y. Lee , and J. Savarino . 2007. “Risk of Suicide Attempt and Suicide Death in Patients Treated for Bipolar Disorder.” Bipolar Disorders 9, no. 5: 526–530. 10.1111/j.1399-5618.2007.00408.x.17680924
- Skinner, H. A. 1982. Guide for Using the Drug Abuse Screening Test (DAST). Centre for Addiction and Mental Health.
- Sletved, K. S. O. , K. Coello , S. Stanislaus , et al. 2022. “Socio‐Economic Status and Functioning in Patients Newly Diagnosed With Bipolar Disorder and Their Unaffected Siblings ‐ Results From a Cross‐Sectional Clinical Study.” Journal of Affective Disorders 310: 404–411. 10.1016/j.jad.2022.05.023.35561888
- Smith, K. A. , and A. Cipriani . 2017. “Lithium and Suicide in Mood Disorders: Updated Meta‐Review of the Scientific Literature.” Bipolar Disorders 19, no. 7: 575–586. 10.1111/bdi.12543.28895269
- Spoorthy, M. S. , S. Chakrabarti , and S. Grover . 2019. “Comorbidity of Bipolar and Anxiety Disorders: An Overview of Trends in Research.” World Journal of Psychiatry 9, no. 1: 7–29. 10.5498/wjp.v9.i1.7.30631749 PMC6323556
- Swann, A. C. , C. L. Bowden , J. R. Calabrese , S. C. Dilsaver , and D. D. Morris . 1999. “Differential Effect of Number of Previous Episodes of Affective Disorder on Response to Lithium or Divalproex in Acute Mania.” American Journal of Psychiatry 156, no. 8: 1264–1266. 10.1176/ajp.156.8.1264.10450271
- Sylvia, L. G. 2015. The Wellness Workbook for Bipolar Disorder: Your Guide to Getting Healthy and Improving Your Mood. New Harbinger Publications.
- Tohen, M. , C. A. Zarate Jr. , J. Hennen , et al. 2003. “The McLean‐Harvard First‐Episode Mania Study: Prediction of Recovery and First Recurrence.” American Journal of Psychiatry 160, no. 12: 2099–2107. 10.1176/appi.ajp.160.12.2099.14638578
- Towle, A. , T. Greenhalgh , J. Gambrill , and W. Godolphin . 1999. “Framework for Teaching and Learning Informed Shared Decision makingCommentary: Competencies for Informed Shared Decision makingCommentary: Proposals Based on Too Many Assumptions.” BMJ 319, no. 7212: 766–771.10488010 10.1136/bmj.319.7212.766PMC1116602
- van der Ven, E. , N. Jones , N. Bareis , et al. 2022. “An Intersectional Approach to Ethnoracial Disparities in Pathways to Care Among Individuals With Psychosis in Coordinated Specialty Care.” JAMA Psychiatry 79, no. 8: 790–798. 10.1001/jamapsychiatry.2022.1640.35767311 PMC9244772
- White, S. , R. Foster , J. Marks , et al. 2020. “The Effectiveness of One‐To‐One Peer Support in Mental Health Services: A Systematic Review and Meta‐Analysis.” BMC Psychiatry 20, no. 1: 534. 10.1186/s12888-020-02923-3.33176729 PMC7657356
- Yarborough, B. J. , M. C. Leo , M. T. Yarborough , et al. 2016. “Improvement in Body Image, Perceived Health, and Health‐Related Self‐Efficacy Among People With Serious Mental Illness: The STRIDE Study.” Psychiatric Services 67, no. 3: 296–301. 10.1176/appi.ps.201400535.26522674 PMC7104613
- Yatham, L. N. , S. H. Kennedy , S. V. Parikh , et al. 2018. “Canadian Network for Mood and Anxiety Treatments (CANMAT) and International Society for Bipolar Disorders (ISBD) 2018 Guidelines for the Management of Patients With Bipolar Disorder.” Bipolar Disorders 20, no. 2: 97–170. 10.1111/bdi.12609.29536616 PMC5947163
- Yu, L. , D. J. Buysse , A. Germain , et al. 2012. “Development of Short Forms From the PROMIS Sleep Disturbance and Sleep‐Related Impairment Item Banks.” Behavioral Sleep Medicine 10, no. 1: 6–24.10.1080/15402002.2012.636266PMC326157722250775
Til din tryghed. MitLivMed er et fællesskab. Vi yder ikke krisestøtte eller medicinsk rådgivning og erstatter ikke din behandler. Fortællinger og mestringsforslag er medlemmernes egne erfaringer. Er du i krise? Find akut hjælp her.