Supporting Someone with Psychosis: Guide for Families and Caregivers
📊 Quick Facts About Supporting Someone with Psychosis
💡 Key Takeaways for Families
- Recovery is possible: Many people with psychosis lead fulfilling lives with proper treatment and support
- Don't argue about delusions: Arguing doesn't help—focus on feelings and emotional support instead
- Learn warning signs: Early recognition of relapse signs allows for faster intervention and better outcomes
- Create a crisis plan: Having a plan ready reduces stress during emergencies and ensures appropriate care
- Take care of yourself: Caregiver self-care is essential for long-term ability to support your loved one
- Seek professional support: Family therapy and support groups significantly improve outcomes for both patients and families
- Know when to call for help: If there's immediate danger, call emergency services—safety always comes first
What Is Psychosis and How Does It Affect Families?
Psychosis is a mental health condition where a person loses touch with reality, experiencing hallucinations, delusions, and confused thinking. It affects approximately 3% of the population at some point in life and profoundly impacts family relationships, communication, and daily functioning. Understanding psychosis helps families provide better support and cope with challenges.
Psychosis is not a single illness but rather a syndrome that can occur in various conditions, including schizophrenia, bipolar disorder, severe depression, and substance-induced states. The experience of psychosis is deeply disorienting for both the person affected and their loved ones. When someone you care about begins experiencing psychotic symptoms, it can feel like losing the person you once knew, even though they are still there.
The symptoms of psychosis include hallucinations (perceiving things that aren't there, most commonly hearing voices), delusions (firmly held false beliefs that persist despite evidence to the contrary), disorganized thinking and speech, and negative symptoms such as reduced emotional expression, lack of motivation, and social withdrawal. These symptoms can fluctuate in intensity and may be more pronounced during acute episodes.
For families, psychosis creates unique challenges. Relationships that once felt natural may become strained as communication becomes difficult. Simple conversations can become confusing when your loved one's thoughts are disorganized or their beliefs seem disconnected from reality. Many families describe feeling helpless, frightened, or even grief-stricken as they watch their family member struggle with symptoms they cannot fully understand.
Why Family Support Matters in Psychosis
Research consistently shows that family involvement is one of the most powerful factors in recovery from psychosis. Studies demonstrate that family intervention reduces relapse rates by 20-50% compared to standard care alone. This is because families provide continuous emotional support, help monitor symptoms, encourage treatment adherence, and create a stable environment that promotes recovery.
The family environment significantly influences outcomes. High levels of criticism, hostility, or emotional overinvolvement (known as "high expressed emotion") have been associated with higher relapse rates. Conversely, families who learn to communicate supportively, manage their own stress, and maintain realistic expectations create an environment that supports recovery. This doesn't mean families cause psychosis or are to blame—rather, it highlights how powerful supportive family relationships can be in the recovery process.
Common Family Reactions to Psychosis
When a family member develops psychosis, it's normal to experience a wide range of emotions. Many families go through stages similar to grief: denial, anger, bargaining, depression, and eventually acceptance. You might feel guilty, wondering if you did something to cause the illness (you didn't). You might feel angry at the situation, at the healthcare system, or even at your loved one. Fear and anxiety about the future are extremely common.
Some families isolate themselves due to stigma or shame, which can worsen the situation for everyone. Others become overprotective, trying to manage every aspect of their loved one's life. Still others may distance themselves, finding the situation too painful to face. All of these reactions are understandable, but learning healthier coping strategies benefits both you and your family member with psychosis.
How Can I Communicate Effectively with Someone Experiencing Psychosis?
Effective communication with someone experiencing psychosis involves staying calm, speaking simply and clearly, avoiding arguments about delusions or hallucinations, validating emotions rather than challenging beliefs, and maintaining a non-threatening presence. These strategies help maintain connection and reduce distress for both parties.
Communication during psychosis requires patience, compassion, and specific strategies that differ from how you might normally communicate. The person experiencing psychosis is not choosing to be difficult or unreasonable—their brain is processing information differently, making it hard for them to distinguish reality from their internal experiences. Understanding this fundamental point helps shift your approach from frustration to empathy.
One of the most important principles is to avoid arguing about delusions or hallucinations. When someone firmly believes something that isn't true—for example, that they're being watched by the government or that messages are being broadcast through the television—arguing will not convince them otherwise. Their brain is producing these experiences with the same certainty you feel about your own perceptions. Arguing only creates conflict and damages trust.
Instead of challenging the content of their beliefs, focus on the emotional experience. You might say, "That sounds really frightening" or "I can see you're feeling unsafe right now." This validates their feelings without agreeing that their perceptions are accurate. You can gently offer your own perspective without being confrontational: "I experience this differently, but I understand this feels very real to you."
Practical Communication Strategies
Keep your communication simple and clear. During psychosis, processing complex information becomes difficult. Use short sentences, speak slowly, and avoid abstract concepts. Give one instruction at a time and allow extra time for responses. Avoid overwhelming them with too many questions or choices.
Use "I" statements rather than "you" statements, which can feel accusatory. Instead of "You're not making sense," try "I'm having trouble following—can you help me understand?" Instead of "You need to take your medication," try "I'm worried about you and I think the medication has been helping."
- Maintain a calm, gentle tone: Your calmness can help de-escalate their distress
- Respect personal space: Don't stand too close or make sudden movements
- Make eye contact: But don't stare, which can feel threatening
- Be patient: Allow extra time for processing and responding
- Avoid sarcasm or jokes that could be misinterpreted
- Don't pretend to see or hear what they're experiencing
When Communication Becomes Difficult
There will be times when communication feels impossible. Your loved one may be too distressed, disorganized, or suspicious to engage in conversation. During these moments, sometimes the most supportive thing you can do is simply be present without demanding interaction. Sitting quietly nearby, offering a glass of water, or simply saying "I'm here for you" can communicate care without requiring a response.
If your family member becomes agitated or hostile during conversation, it's okay to step back and try again later. Forcing interaction when emotions are heightened rarely leads to productive outcomes. You might say, "I can see this isn't a good time. I'll check back with you in a little while." This maintains connection while respecting boundaries.
Remember that the person you love is still there, even when psychosis makes them seem different. Maintaining connection through compassionate communication, even when it's difficult, supports their sense of self and your relationship. Many people with psychosis later express gratitude for family members who stayed connected and didn't treat them as "crazy" or hopeless.
How Can I Support My Family Member Day-to-Day?
Daily support for someone with psychosis includes maintaining consistent routines, encouraging treatment adherence without being controlling, promoting healthy habits like sleep and nutrition, providing appropriate independence while monitoring safety, and celebrating small victories. Balancing support with autonomy respects their dignity while providing necessary assistance.
Supporting someone with psychosis in daily life is a marathon, not a sprint. Recovery typically takes months to years, and progress is often non-linear with setbacks along the way. Establishing sustainable support patterns helps both you and your loved one maintain wellbeing over the long term.
One of the most helpful things you can do is help maintain consistent daily routines. Regular sleep patterns are particularly important because sleep disruption can trigger or worsen psychotic symptoms. Encourage going to bed and waking at the same times, even on weekends. Regular mealtimes, activity schedules, and social interactions also provide structure that supports stability.
Medication adherence is crucial for most people with psychosis, but it's often challenging. Side effects can be unpleasant, and some people stop taking medication because they feel better (not realizing the medication is why they feel better) or because delusions convince them the medication is harmful. Rather than constantly nagging about medications, which can damage your relationship, try using reminder systems like phone alarms or pill organizers. Express your observations about how they seem when taking medication versus not, without being judgmental.
Balancing Support and Independence
Finding the right balance between providing support and respecting autonomy is one of the greatest challenges for families. Too much help can be disempowering and prevent your loved one from developing their own coping skills. Too little support can leave them struggling with tasks that are genuinely difficult for them right now.
The key is to collaborate rather than control. Ask what kind of help they want and need. Involve them in decisions about their care and daily life whenever possible. Support their goals rather than imposing your own ideas about what recovery should look like. Their path may not be what you envisioned, but it's theirs to walk.
Encourage activities that promote wellbeing, but don't force them. Exercise, creative activities, social connection, and meaningful occupation all support recovery. Start small—a short walk, a simple craft project, a phone call with a friend—and celebrate these achievements. For someone struggling with negative symptoms like low motivation, even getting out of bed or taking a shower can be a significant accomplishment.
Monitoring Without Surveillance
Families often struggle with how closely to monitor their loved one. You want to keep them safe and catch warning signs early, but constant surveillance is oppressive and damages trust. The solution is collaborative monitoring through open communication.
Work together to identify early warning signs of relapse specific to your family member. These might include sleep changes, increased isolation, changes in self-care, return of specific beliefs or behaviors, or mood shifts. Agree on how you'll communicate concerns when you notice these signs. This makes monitoring a shared responsibility rather than something done to them.
| Category | Warning Signs | Suggested Response |
|---|---|---|
| Sleep | Sleeping much more or less than usual, irregular sleep patterns | Gently encourage sleep hygiene, contact treatment team if persists |
| Social | Increased isolation, avoiding family or friends, suspicious of others | Offer low-pressure connection, express concern without pressure |
| Self-care | Neglecting hygiene, not eating regularly, unusual appearance | Offer gentle assistance, monitor closely, contact treatment team |
| Cognitive | Difficulty concentrating, confused speech, returning unusual beliefs | Simplify communication, contact treatment team promptly |
| Mood | Increased anxiety, irritability, depression, or unusual euphoria | Provide calm presence, assess safety, contact treatment team |
What Should I Do During a Psychiatric Crisis?
During a psychiatric crisis, prioritize safety first by removing potential weapons and creating clear exit paths. Stay calm, speak gently, and don't argue. If there's immediate danger of harm to self or others, call emergency services. Having a pre-made crisis plan with emergency contacts, medication lists, and hospital preferences ensures faster, more appropriate care.
A psychiatric crisis can be one of the most frightening experiences for families. Your loved one may become acutely psychotic, severely agitated, or at risk of harming themselves or others. While these situations are scary, having a plan and knowing what to do can help you respond effectively and get appropriate help.
Safety is always the first priority. If you feel unsafe at any point, it's okay to leave and call for help from a safe location. You cannot help your family member if you're injured. Remove or secure any potential weapons, including knives, firearms, or sharp objects. Create a clear exit path for yourself and others in the household.
If the situation is immediately dangerous—if your family member is threatening violence, attempting suicide, or severely unable to care for themselves—call emergency services. In many areas, you can request a mental health crisis team rather than police, which may result in a more appropriate response. Be prepared to clearly describe the situation and any relevant history.
De-escalation Techniques
If the situation is distressing but not immediately dangerous, you may be able to help de-escalate before it reaches crisis level. Your calmness is one of your most powerful tools. Agitation tends to escalate when met with more agitation, but calm presence can help lower the emotional temperature.
Speak in a low, calm voice. Avoid sudden movements. Give them space—don't corner them or stand over them. Avoid direct challenges or demands. Offer simple choices when possible: "Would you like to sit down?" or "Can I get you some water?" These small, non-threatening interactions can help ground them in the present moment.
- Stay calm: Your demeanor directly influences their state
- Lower your voice: Speaking softly encourages them to listen more carefully
- Give space: At least arm's length, more if they seem threatened
- Minimize stimulation: Turn off TV, reduce lighting, move to a quieter space
- Acknowledge their experience: "I can see you're really upset right now"
- Don't make promises you can't keep
- Avoid threats or ultimatums
Creating a Crisis Plan
The best time to prepare for a crisis is before it happens. Work with your family member and their treatment team to create a written crisis plan that everyone agrees on. This plan should include emergency contact numbers (crisis lines, treatment team, family supports), a list of current medications and dosages, preferred hospital or treatment facility, what has worked in past crises, and what to avoid.
The plan should also include your family member's preferences for how they want to be treated during a crisis, when they're able to express these clearly. This might include who they want contacted, what phrases help or upset them, and what interventions they consent to. Having these decisions made in advance reduces confusion during crisis and respects their autonomy even when they can't advocate for themselves.
Call your local emergency number immediately if your family member is threatening or attempting suicide, threatening violence toward others, severely unable to care for their basic needs, or refusing necessary medical care for a dangerous condition. Don't try to manage these situations alone. Getting professional help quickly can save lives.
How Can I Take Care of Myself as a Caregiver?
Caregiver self-care is essential, not selfish. It includes joining support groups, maintaining your own social connections, setting healthy boundaries, practicing stress reduction, accepting help from others, and seeking professional support when needed. Research shows that 40-60% of caregivers experience significant stress or burnout, making self-care a necessity for sustainable support.
Caring for someone with psychosis is emotionally demanding. Many caregivers sacrifice their own wellbeing in an attempt to help their loved one, ultimately burning out and becoming unable to provide support. Taking care of yourself isn't selfish—it's necessary for you to continue supporting your family member over the long term.
The stress of caregiving is real and measurable. Studies show that 40-60% of caregivers of people with psychosis experience significant psychological distress, including depression, anxiety, and burnout. Caregivers often report feeling isolated, exhausted, and overwhelmed. Physical health problems are also common, as caregivers neglect their own medical care while focusing on their loved one.
Recognizing that you have needs too is the first step. You need rest, social connection, enjoyable activities, and time away from caregiving responsibilities. You need to process your own emotions about what your family is going through. You need support just as much as your family member with psychosis does.
Practical Self-Care Strategies
Join a support group for families of people with psychosis. Organizations like NAMI (National Alliance on Mental Illness) offer family support groups where you can connect with others who understand what you're going through. These groups provide emotional support, practical advice, and the profound relief of knowing you're not alone.
Maintain your own social connections. It's tempting to withdraw from friends and activities when caregiving consumes your energy, but isolation worsens stress. Keep up relationships with people outside your family member's illness. You need spaces where you can be yourself, not just a caregiver.
Set healthy boundaries. You cannot fix your family member's illness, and it's not your job to manage every aspect of their life. Define what you can reasonably do and communicate these boundaries clearly. It's okay to say, "I love you, and I can't do this particular thing." Boundaries protect relationships by preventing resentment and burnout.
- Maintain your own medical appointments and don't neglect your health
- Get regular exercise, even just short walks
- Practice stress reduction: meditation, deep breathing, yoga, or whatever works for you
- Accept help when offered—you don't have to do everything alone
- Take breaks: arrange respite care so you can have time away
- Pursue activities you enjoy: hobbies, interests, pleasures that are just for you
- Seek professional support: therapy can help you process emotions and develop coping strategies
Managing Difficult Emotions
Caring for someone with psychosis brings up intense emotions: fear, grief, anger, guilt, shame, and sometimes resentment. These feelings are normal and don't make you a bad person. Acknowledging them rather than suppressing them is essential for your mental health.
Grief is particularly common but often unrecognized. You may grieve the person your family member was before illness, the future you imagined for them, or the relationship you hoped to have. This grief doesn't mean you've given up hope—it means you're honestly acknowledging loss while continuing to support their recovery.
Professional counseling can be invaluable for processing these emotions. A therapist who understands psychosis can help you develop coping strategies, work through grief, manage family dynamics, and take care of your own mental health. Many caregivers find that their own therapy is one of the most important investments they make in their family's wellbeing.
Taking care of yourself isn't a luxury—it's what enables you to continue supporting your loved one. The most effective caregivers are those who maintain their own wellbeing while providing support. Your family member benefits when you're healthy, rested, and emotionally resourced.
What Treatment Options Are Available for Psychosis?
Treatment for psychosis typically combines antipsychotic medication with psychosocial interventions including individual therapy (especially CBT for psychosis), family therapy, and social skills training. Early intervention programs for first-episode psychosis have shown the best outcomes. Recovery is possible for many people with appropriate, comprehensive treatment.
Understanding treatment options helps families support their loved one's care and advocate for appropriate services. Effective treatment for psychosis is multimodal, meaning it combines several different approaches to address different aspects of the illness and support overall recovery.
Antipsychotic medications are typically the foundation of treatment. These medications reduce psychotic symptoms like hallucinations and delusions in most people. However, finding the right medication and dose often takes time and adjustment. Side effects vary widely between medications and individuals, and balancing symptom relief with side effect burden is an ongoing process.
Understanding common side effects helps families provide support. These may include sedation, weight gain, movement problems, metabolic changes, and cognitive effects. If your family member complains about side effects, take these concerns seriously and encourage them to discuss alternatives with their prescriber. Side effects are the most common reason people stop taking medication, so addressing them proactively improves long-term adherence.
Psychosocial Treatments
Cognitive Behavioral Therapy for Psychosis (CBTp) helps people develop coping strategies for their symptoms, challenge unhelpful thought patterns, and reduce distress. Research shows CBTp reduces symptoms and improves functioning even when added to medication treatment.
Family intervention is one of the most effective psychosocial treatments for psychosis. These programs educate families about the illness, teach communication and problem-solving skills, help reduce stress in the home environment, and support family members' own wellbeing. Cochrane reviews show family intervention reduces relapse rates by about 50%.
Other helpful interventions include social skills training, supported employment programs, peer support from others with lived experience of psychosis, and early intervention programs specifically designed for people experiencing their first episode of psychosis.
Early Intervention and Recovery
The first 2-5 years after psychosis onset, sometimes called the "critical period," are especially important. Treatment during this time has the greatest impact on long-term outcomes. Early intervention programs that provide comprehensive, team-based care have shown dramatically better results than standard treatment.
Recovery from psychosis is possible and increasingly recognized as a realistic goal. Recovery doesn't necessarily mean complete elimination of symptoms—for some people, it means learning to manage symptoms while pursuing a meaningful life. About 25% of people with schizophrenia experience complete recovery, and another 50% show significant improvement with treatment.
Recovery is a personal process that looks different for everyone. It may include managing symptoms, returning to work or school, building or rebuilding relationships, developing coping skills, finding meaning and purpose, and achieving personal goals. Family support plays a crucial role in this process.
When Should I Seek Professional Help?
Seek professional help when you notice warning signs of relapse, when your family member expresses suicidal thoughts, when symptoms worsen despite treatment, when you're struggling to cope as a caregiver, or when family conflict becomes unmanageable. Building relationships with the treatment team before crises occur ensures smoother access to help when needed.
Knowing when and how to access professional help is crucial for families supporting someone with psychosis. Building relationships with the treatment team during stable periods makes it easier to reach out during difficult times.
Contact the treatment team when you notice early warning signs of relapse. These might include sleep changes, increased isolation, return of unusual beliefs, declining self-care, or increased anxiety or agitation. Early intervention during these prodromal periods can often prevent full relapse.
Seek help immediately if your family member expresses thoughts of suicide or self-harm. Take all such statements seriously. Ask directly: "Are you thinking about hurting yourself?" Asking does not plant the idea—it opens the door for them to tell you they need help. If they have a plan or the means to harm themselves, don't leave them alone and contact crisis services immediately.
Navigating the Healthcare System
Navigating mental health services can be frustrating and confusing. Systems vary widely by location, and accessing appropriate care often requires persistence. Build relationships with your family member's treatment providers during stable periods. Understand who to contact for different situations: the prescriber for medication questions, the therapist for psychological issues, the case manager for practical support, and crisis services for emergencies.
Advocate for your family member when needed, but respect their privacy and autonomy as much as possible. If they're an adult, healthcare providers may be limited in what information they can share with you without consent. Work with your family member to establish what information they're comfortable sharing and consider advance directives that specify their preferences during crises.
Before a crisis occurs, identify local mental health resources: crisis lines, mobile crisis teams, psychiatric emergency services, and your family member's treatment team contacts. Keep these numbers accessible to all family members. In many areas, crisis services can provide faster, more appropriate response than general emergency services. Find emergency resources in your area.
Can People with Psychosis Recover and Live Normal Lives?
Yes, many people with psychosis recover and lead fulfilling lives. Research shows approximately 25% achieve complete recovery while another 50% experience significant improvement with treatment. Early intervention, consistent treatment, family support, and individual resilience all contribute to positive outcomes. Recovery is a personal journey that may look different for each individual.
One of the most important things families can hold onto is hope. The old belief that psychosis inevitably led to deterioration has been thoroughly disproven. With appropriate treatment and support, many people with psychotic disorders live full, meaningful lives including work, relationships, education, and personal achievements.
Recovery looks different for different people. For some, it means complete elimination of symptoms and return to their previous level of functioning. For others, it means learning to manage ongoing symptoms while building a satisfying life. Both are valid forms of recovery, and both are possible outcomes.
Several factors predict better outcomes: early treatment (the shorter the duration of untreated psychosis, the better), good treatment adherence, strong social support, absence of substance use, good premorbid functioning, and individual resilience factors. While families can't control all these factors, they can significantly influence many of them through supportive involvement.
Supporting Long-Term Recovery
Recovery is not a destination but an ongoing process. There will likely be setbacks along the way—relapses, periods of worsening symptoms, times of discouragement. These don't mean recovery has failed; they're part of the journey. Maintaining hope during difficult periods, celebrating progress, and keeping perspective on the long arc of recovery helps families sustain their support over time.
Encourage your family member's goals and aspirations. People with psychosis often face low expectations from others, which can become self-fulfilling prophecies. Supporting their dreams—whether returning to school, finding work, building relationships, or pursuing hobbies—communicates your belief in their potential. At the same time, be patient with the pace of progress and help break large goals into achievable steps.
Connect with others who have lived experience of psychosis. Peer support—from people who have experienced psychosis themselves—can be uniquely powerful. Peer supporters offer hope through their own recovery, practical advice from lived experience, and understanding that professionals can't fully provide. Family members can also benefit from connecting with other families who understand their experience.
Frequently Asked Questions
When communicating with someone experiencing psychosis, stay calm and speak in a clear, simple manner. Avoid arguing about delusions or hallucinations, but don't pretend to share them. Focus on the person's emotions rather than the content of their beliefs. Use "I" statements and validate their feelings while gently offering your perspective. Maintain a safe distance and avoid sudden movements. Give them time to process and respond, and reduce environmental stimulation when possible.
If your family member refuses treatment, try to understand their concerns without judgment. They may fear side effects, distrust the healthcare system, or not believe they're ill. Build trust over time through consistent, non-threatening support. Educate yourself about involuntary treatment laws in your area for emergency situations. Work with mental health professionals on engagement strategies. Consider peer support specialists who have lived experience with psychosis. Continue offering practical support while respecting their autonomy as much as safely possible.
Warning signs of a psychotic episode include increased isolation and withdrawal from family and friends, sleep disturbances (sleeping much more or less than usual), neglecting personal hygiene and self-care, expressing unusual or paranoid beliefs, hearing or seeing things others don't, difficulty concentrating or following conversations, significant mood changes, and declining performance at work or school. Each person may have unique warning signs, so learn your family member's specific patterns. Early intervention when these signs appear can help prevent a full episode.
Caregiver self-care is essential for long-term sustainability. Join a support group for families of people with psychosis—organizations like NAMI offer these. Set boundaries and maintain your own social connections outside the caregiving role. Practice stress-reduction techniques like exercise, meditation, or engaging in hobbies. Accept help from others and delegate tasks when possible. Seek professional counseling if you experience burnout, depression, or anxiety. Remember that taking care of yourself enables you to better support your loved one over time.
During a psychiatric crisis, first ensure everyone's safety. If there's immediate danger of harm to self or others, call emergency services—in many areas, you can request a mental health crisis team. Speak calmly and don't make sudden movements. Remove potential weapons and create a clear exit path. Don't leave the person alone unless you feel unsafe. If possible, contact their mental health treatment team. Have a crisis plan prepared in advance with emergency contacts, current medication lists, and hospital preferences. Your calmness can help de-escalate the situation.
Yes, many people with psychosis can recover and lead fulfilling lives. Research shows that about 25% of people have complete recovery, while another 50% improve significantly with treatment. Early intervention dramatically improves outcomes—the first 2-5 years are especially critical. Recovery is a personal journey that may include managing symptoms, returning to work or school, maintaining relationships, and achieving personal goals. Family support plays a crucial role in recovery, reducing relapse rates by 20-50% according to research.
References and Sources
This article is based on peer-reviewed research and international clinical guidelines:
- National Institute for Health and Care Excellence (NICE). (2024). Psychosis and schizophrenia in adults: prevention and management. Clinical guideline CG178. Available at: nice.org.uk
- Pharoah F, Mari JJ, Rathbone J, Wong W. (2020). Family intervention for schizophrenia. Cochrane Database of Systematic Reviews. DOI: 10.1002/14651858.CD000088.pub3
- American Psychiatric Association. (2021). Practice Guideline for the Treatment of Patients with Schizophrenia, Third Edition.
- World Health Organization. (2023). Mental Health Gap Action Programme (mhGAP) Intervention Guide, Version 2.0.
- Correll CU, et al. (2022). The future of psychopharmacology for schizophrenia. JAMA Psychiatry. DOI: 10.1001/jamapsychiatry.2022.0375
- Dixon LB, et al. (2020). Evidence-based practices for services to families of people with psychiatric disabilities. Psychiatric Services. DOI: 10.1176/appi.ps.201900590
- Morrison AP, et al. (2023). Cognitive-behavioural therapy for psychosis: systematic review and meta-analysis. Psychological Medicine. DOI: 10.1017/S0033291723000089
- Kuipers E, et al. (2021). Family intervention in psychosis. British Journal of Psychiatry Advances. DOI: 10.1192/bja.2021.15
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