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Healthcare Interview Prep

NHS INTERVIEW PREPARATION

Psychiatry - Learning Disability Interview Questions & Answers

40 NHS interview questions with model answers · 8 free to read

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About this NHS interview question bank

To prepare for a learning disability psychiatry NHS interview, expect questions on diagnostic overshadowing, assessing mental illness in people who communicate without many words, behaviours that challenge and positive behaviour support, STOMP and psychotropic prescribing, epilepsy, autism, the Mental Capacity Act and keeping people out of hospital through Care (Education) and Treatment Reviews. Build short spoken answers around real cases from your practice, and know the GMC's Good Medical Practice, the NHS values, LeDeR and Building the Right Support before you walk in.

This bank contains 40 original practice questions with first-person model answers written for doctors applying to learning disability psychiatry posts, pitched mainly at Clinical Fellow and Specialty Doctor level, with a selection aimed at Specialist and Consultant interviews. It covers community learning disability teams, inpatient and assessment settings, and the interface with families, paid carers, GPs and acute hospitals. Every question explains what the panel is really assessing, the points you must hit, the mistakes to avoid and the frameworks worth reading, so you can practise answers that sound like a thoughtful, safe psychiatrist rather than a textbook.

 

What this question bank covers

  • Motivation for learning disability psychiatry
  • NHS values and health inequalities
  • Diagnostic overshadowing
  • Assessing mental illness with limited verbal communication
  • Behaviours that challenge and positive behaviour support
  • STOMP and psychotropic prescribing
  • Epilepsy and mental health
  • Autism
  • Dementia in Down syndrome
  • Mental Capacity Act and best interests
  • Mental Health Act and learning disability
  • Transforming Care, Building the Right Support and C(E)TRs
  • LeDeR
  • Working with families and paid carers
  • Reasonable adjustments and annual health checks
  • Safeguarding adults and children
  • Confidentiality and record keeping
  • Patient safety and learning
  • Leadership at Specialty Doctor, Specialist and Consultant level
  • Resilience and wellbeing

 

40 NHS interview questions with full model answers. The first 8 are free to read below. Unlock the remaining 32 for £2.99 (12 months' access).

These are original practice questions written to reflect how NHS interviews are run. They are not leaked or official questions, and Healthcare Interview Prep is independent of the NHS.

 

 

Free NHS interview questions and model answers

 

 

Question 1: Why do you want to work in the psychiatry of learning disability?

Motivation question  ·  Motivation

 

What the interview panel is assessing

The panel wants a genuine, personal reason rather than a line about liking a quieter specialty. They are listening for an understanding of the health inequalities people with a learning disability face, and for realism about the slower, relationship-based nature of the work.

 

Model answer

I can point to the patient who changed my thinking. During a general adult rotation I was asked to see a man in his forties with a moderate learning disability who'd been referred because he'd "become aggressive" at his supported living house. The referral asked for something to calm him down. When I sat with him and his support worker, he kept pressing his hand against his jaw. Nobody had joined those dots. He had a dental abscess, and once that was treated the so-called aggression stopped.

That stayed with me, because it could so easily have ended with an antipsychotic and a label. It showed me that in this specialty the psychiatry is only part of the job. You're a detective, a translator and quite often an advocate, and you have to keep asking whether what you're seeing is mental illness, physical pain, an environment that isn't working, or simply someone trying to tell you something.

I also like the pace and the relationships. You might know a patient and their family for years. You work closely with nurses, psychologists, speech and language therapists, occupational therapists and behaviour specialists, and the best outcomes come from that team thinking together rather than from a prescription.

I'm realistic about the hard parts. People with a learning disability still die younger than the general population, often from things that could have been prevented, and services can be stretched. Some of the decisions around capacity, restriction and admission are genuinely difficult. That doesn't put me off. It's exactly why I want to be a doctor in this field, and why I'd like to build my career here rather than pass through it.

 

Why this answer works

The answer opens with a concrete clinical story that shows diagnostic overshadowing without lecturing about it. It demonstrates an understanding of the multidisciplinary, long-term nature of the work and acknowledges health inequalities honestly, which signals commitment rather than convenience.

 

Key points to include

  • A specific moment or patient that shaped your interest
  • Recognition that behaviour change may have a physical or environmental cause
  • Valuing the multidisciplinary team and long-term relationships
  • Awareness of health inequalities and premature mortality
  • Commitment to the specialty, not just the post

 

Common mistakes to avoid

  • Implying the specialty is easier or less acute than general adult psychiatry
  • Speaking about patients in a pitying or patronising way
  • Giving a generic answer that could apply to any psychiatry post
  • Ignoring families, carers and the wider team

 

NHS values and standards

Compassion; Everyone counts; Improving lives; GMC Good Medical Practice: patients, partnership and communication

 

Further reading

  • GMC Good Medical Practice
  • Royal College of Psychiatrists: Faculty of Psychiatry of Intellectual Disability resources
  • LeDeR (Learning from lives and deaths) annual reports
  • NHS Constitution for England

 

 

Question 2: Which NHS value matters most to you in learning disability psychiatry, and can you give an example of living it?

NHS Values question  ·  NHS Values

 

What the interview panel is assessing

The panel is checking you know the NHS values and can link one to everyday behaviour in this specialty. They want a real example, ideally showing how easily people with a learning disability can be overlooked, and what you did about it.

 

Model answer

The six NHS values are working together for patients, respect and dignity, commitment to quality of care, compassion, improving lives, and everyone counts. In this specialty I keep coming back to everyone counts, because the evidence from programmes like LeDeR shows that people with a learning disability are too often treated as if their symptoms are just part of their disability.

A while ago I was covering a community clinic and saw a young woman with a severe learning disability and very little speech. Her mum said she'd been crying at night and pulling at her clothes for several weeks. The previous letter said "behavioural, likely sensory, review in six months." Something didn't sit right with me. I asked about her periods, her bowels, her sleep and whether anything had changed at home or at day services. Mum mentioned the crying seemed worse around her period, and she hadn't opened her bowels properly for days at a time.

I didn't want to start a psychotropic for something that might be pain. I wrote to the GP asking for a physical review, including constipation and menstrual pain, and suggested a simple diary that mum and the day centre could both fill in. We used a distress assessment tool so we had a baseline of what "content" and "distressed" looked like for her. Once her constipation was treated and her GP discussed options for period pain, the night-time distress settled a great deal.

What I took from it is that "everyone counts" isn't a poster on the wall. It means giving someone who can't tell you what's wrong the same careful thinking you'd give anyone else, and not accepting "it's just her learning disability" as an explanation.

 

Why this answer works

The candidate names the values accurately, picks one and grounds it in a believable case of diagnostic overshadowing. The answer shows practical steps, joint working with family and GP, and avoidance of unnecessary medication, which ties the value to safe practice.

 

Key points to include

  • Name the NHS values accurately
  • Choose one and explain why it matters in this specialty
  • A specific example where someone could have been overlooked
  • Practical actions: physical health review, diary, distress tool, joint working
  • Reflection on what the value means day to day

 

Common mistakes to avoid

  • Listing all the values without an example
  • Choosing a value but describing generic kindness
  • Jumping to medication in the example
  • Not involving the family or GP

 

NHS values and standards

Everyone counts; Respect and dignity; Compassion; GMC Good Medical Practice

 

Further reading

  • NHS Constitution for England
  • LeDeR (Learning from lives and deaths) reports
  • NICE guideline: Mental health problems in people with learning disabilities
  • Disability Distress Assessment Tool (DisDAT) guidance

 

 

Question 3: How would you assess for a mental illness in someone with a severe learning disability who has very limited verbal communication?

Communication question  ·  Communication

 

What the interview panel is assessing

This tests whether you can adapt a psychiatric assessment when the usual tools of interview and self-report are not available. The panel wants to hear about observation, informants, baselines, physical causes and the multidisciplinary team, and an awareness of diagnostic overshadowing.

 

Model answer

The first thing I remind myself is that I can't rely on the person telling me about low mood, voices or worries, so I have to build the picture from several sources and from change over time.

I'd start with the people who know them best: family, paid carers, day service staff. My key question is always "what's different from their usual self?" So I'd want to know their baseline in detail: sleep, appetite, weight, how they spend the day, what they enjoy, how they usually show they're unhappy. Then I'd look for change. Withdrawal from things they used to love, loss of skills, new self-injury, changes in sleep or eating, crying, agitation or a sudden drop in self-care can all point towards depression, for example, even when the person can't say they feel low.

I'd also meet the person somewhere familiar where possible, with someone they trust, and use whatever communication they do use: objects of reference, signing, pictures or a communication passport. A speech and language therapist can be invaluable here. I'd observe them over more than one visit, because one snapshot can be misleading.

Alongside that I'd think hard about physical causes, because pain and illness often present as behaviour change. Constipation, dental problems, reflux, infections, epilepsy, thyroid problems, menstrual pain and medication side effects all need ruling out with the GP. And I'd look at the environment: a change of staff, a bereavement, a move or a noisy new housemate.

To make the assessment more objective I'd use structured observation, such as sleep and mood charts, and adapted diagnostic criteria like DC-LD as a guide, being careful not to over-interpret. Finally, I'd discuss it with the multidisciplinary team and my consultant, because these are often complex formulations and it's safer to share the thinking than to rush to a diagnosis or a prescription.

 

Why this answer works

The answer is structured around informants, baseline and change, communication adaptations, physical health, environment and structured tools. It shows awareness of diagnostic overshadowing and the value of the MDT, and it ends with appropriate senior discussion rather than a quick prescription.

 

Key points to include

  • Collateral history focused on baseline and change
  • Adapting communication, involving speech and language therapy
  • Systematic exclusion of physical causes such as pain and epilepsy
  • Considering environmental and life-event triggers
  • Structured observation and adapted diagnostic criteria
  • MDT formulation and senior discussion

 

Common mistakes to avoid

  • Treating behaviour change as automatically psychiatric
  • Relying on a single appointment in clinic
  • Not asking what the person is usually like
  • Forgetting medication side effects and epilepsy

 

NHS values and standards

Compassion; Commitment to quality of care; Everyone counts; GMC Good Medical Practice: knowledge, skills and development

 

Further reading

  • NICE guideline: Mental health problems in people with learning disabilities: prevention, assessment and management
  • Royal College of Psychiatrists: DC-LD (Diagnostic Criteria for Psychiatric Disorders for Use with Adults with Learning Disabilities)
  • Mental Capacity Act 2005 Code of Practice
  • Accessible Information Standard

 

 

Question 4: Tell us about how you work with a community learning disability team. What does a good MDT bring to your patients?

Teamwork question  ·  Teamwork

 

What the interview panel is assessing

The panel wants to know that you see the psychiatrist as one member of a team, not the person who simply prescribes. They are looking for respect for other professions and a concrete example where joint working changed an outcome.

 

Model answer

In a community learning disability team the psychiatrist is one voice among many, and honestly some of my best decisions have come from a nurse or therapist pointing out something I'd missed.

One example that stays with me was a young man with autism and a moderate learning disability whose placement was at risk because of hitting out at staff. The provider was pushing for an increase in his risperidone. At our weekly allocation meeting I suggested we didn't do anything to the medication until we had a shared picture. The community nurse visited and did a physical health check and found he'd lost weight. The speech and language therapist realised staff were using long verbal instructions he couldn't process. Our occupational therapist did a sensory assessment and found the communal lounge was overwhelming in the evenings. The behaviour practitioner started ABC charts, which showed most incidents happened at shift change around teatime.

Putting that together, it wasn't a mental illness getting worse. He was hungry, overloaded and confused by inconsistent routines. The team worked with the provider on a positive behaviour support plan, a visual schedule, a quieter space and a snack before shift change. Incidents dropped considerably and, a few months later, I was able to start slowly reducing his risperidone with his family's agreement.

My part was to hold the medical overview: rule out physical illness, review the medication properly, and give the family and provider a clear explanation of the plan. But the plan itself belonged to the whole team. I try to make sure I listen at MDT meetings, share my reasoning openly, and write letters that everyone, including the person and their family, can understand.

 

Why this answer works

The example shows each professional's unique contribution and how combining them led to a better formulation. It positions the psychiatrist as holding the medical overview while valuing others, and links teamwork to a reduction in medication, which fits STOMP.

 

Key points to include

  • The psychiatrist's role within the MDT, not above it
  • A concrete example showing different professions' input
  • Use of ABC charts, sensory and communication assessments
  • Shared formulation leading to a positive behaviour support plan
  • Linking good teamwork to reduced reliance on medication

 

Common mistakes to avoid

  • Describing the MDT only as people you refer to
  • Taking sole credit for a team outcome
  • Not naming specific professions or their roles
  • Giving an example with no clear outcome

 

NHS values and standards

Working together for patients; Respect and dignity; Improving lives; GMC Good Medical Practice: working collaboratively with colleagues

 

Further reading

  • NICE guideline: Challenging behaviour and learning disabilities: prevention and interventions
  • NICE guideline: Learning disabilities and behaviour that challenges: service design and delivery
  • Royal College of Psychiatrists guidance on the role of the psychiatrist in learning disability services
  • STOMP (Stopping over-medication of people with a learning disability, autism or both)

 

 

Question 5: During a home visit to a supported living service you notice bruises on a patient's arms, and staff give vague explanations. What do you do?

Safeguarding question  ·  Safeguarding

 

What the interview panel is assessing

This is a core adult safeguarding scenario. The panel wants to see that you act on concern rather than certainty, keep the person safe, follow the Care Act 2014 process and local policy, and do not try to investigate alone.

 

Model answer

My first priority would be the person in front of me. I'd want to know whether they're in immediate danger and whether they need medical attention. If they could communicate, I'd try to speak with them privately, in a way they understand, without leading questions. If they couldn't, I'd observe how they are with different staff, and whether they seem frightened or withdrawn.

I'd examine the bruises with consent, or in their best interests if they lacked capacity for that decision, and document carefully: size, shape, colour and location, with a body map, and exactly what each staff member said, in their own words. Bruises on the upper arms can suggest grip marks, so the pattern matters. I'd also think about other explanations, such as falls related to epilepsy, anticoagulants or a blood disorder, and ask the GP for review if needed. But I'd be clear in my own mind that I don't have to be certain abuse has happened to raise a concern. Reasonable cause to suspect is enough.

If there was immediate risk, I'd contact the police or arrange for the person to be somewhere safe. Otherwise I'd discuss with my consultant and the trust safeguarding lead the same day, and make a referral to the local authority adult safeguarding team in line with the Care Act and local procedures. I wouldn't confront staff or tell the provider manager in a way that could put the person at risk or compromise any enquiry.

Wherever possible I'd involve the person and think about what they'd want, which is the idea behind Making Safeguarding Personal. I'd consider whether other residents could be at risk too, because in closed environments problems are rarely limited to one person. Finally, I'd record clearly what I saw, what I did and who I told, and follow up to make sure action had actually been taken.

 

Why this answer works

The answer prioritises immediate safety and medical needs, uses careful documentation and keeps an open mind about alternative explanations without dismissing concern. It follows the correct escalation route under the Care Act and recognises the risk of closed cultures in care settings.

 

Key points to include

  • Immediate safety and medical needs first
  • Speak to the person where possible; observe if not
  • Accurate documentation with body map and verbatim accounts
  • Reasonable suspicion is enough to refer; do not investigate alone
  • Escalate to consultant, safeguarding lead and local authority
  • Consider other residents and closed cultures

 

Common mistakes to avoid

  • Waiting for certainty before raising a concern
  • Confronting staff or the provider directly
  • Accepting vague explanations at face value
  • Forgetting to involve the person or consider their wishes

 

NHS values and standards

Respect and dignity; Compassion; Everyone counts; GMC Good Medical Practice: safeguarding vulnerable people

 

Further reading

  • Care Act 2014 and statutory guidance
  • Making Safeguarding Personal
  • Mental Capacity Act 2005 Code of Practice
  • GMC guidance: Protecting children and young people and adult safeguarding duties
  • Local multi-agency safeguarding adults procedures

 

 

Question 6: A GP asks you to review a man with a moderate learning disability who has been on an antipsychotic for ten years with no diagnosis of psychosis. How would you approach this?

Clinical Scenario question  ·  Clinical Scenario

 

What the interview panel is assessing

This tests your knowledge of STOMP and your ability to review psychotropic medication safely. The panel wants a careful, collaborative approach rather than abrupt withdrawal, with attention to capacity, families, side effects and monitoring.

 

Model answer

This is exactly the kind of referral STOMP was set up for, so I'd welcome it, but I'd approach it carefully rather than just stopping the tablet.

First I'd find out why the antipsychotic was started. I'd go through the GP and hospital records, old clinic letters and speak to family and carers. Often it was started for behaviours that challenge during a crisis, a move or a hospital admission, and never reviewed. I'd want to know what the behaviour was then, what it's like now, and what else has changed.

Then I'd meet him with the people who know him best. I'd assess for any underlying mental illness that might genuinely need treatment, and I'd look for side effects: weight gain, sedation, constipation, swallowing problems, movement disorders, raised prolactin. I'd check whether he's had recent bloods, an ECG if indicated, and his annual health check. I'd assess his capacity to make decisions about his medication and, if he lacks it, make a best interests decision with his family, carers and the GP, involving an advocate if appropriate.

If there's no clear ongoing indication, I'd suggest a slow, planned reduction, rather than stopping abruptly, with agreed monitoring. That means behaviour charts, sleep and a named contact if things go wrong. Withdrawal effects and rebound symptoms can look like a return of the original behaviour, so I'd explain that to everyone in advance. I'd also want support in place, ideally a positive behaviour support plan, so that we're replacing the medication with something better, not just removing it.

Sometimes a reduction doesn't work and we agree the lowest effective dose. That's fine as long as it's a thought-through decision. Throughout, I'd document the rationale clearly, keep the GP informed and review regularly with my consultant.

 

Why this answer works

The answer shows clear STOMP principles: establishing the original indication, assessing for side effects and illness, involving the person and those close to them, applying the Mental Capacity Act and planning a gradual, monitored reduction with behavioural support. It is realistic that withdrawal is not always possible.

 

Key points to include

  • Establish the original reason for prescribing
  • Assess for mental illness and side effects, including physical monitoring
  • Capacity assessment and best interests involvement
  • Slow, planned reduction with monitoring and a contingency plan
  • Put positive behaviour support in place alongside
  • Clear documentation and communication with the GP

 

Common mistakes to avoid

  • Stopping the antipsychotic abruptly
  • Assuming all antipsychotic use is inappropriate
  • Not involving family, carers or an advocate
  • Forgetting withdrawal effects and how they can look like relapse

 

NHS values and standards

Commitment to quality of care; Improving lives; Working together for patients; GMC Good Practice in prescribing and managing medicines and devices

 

Further reading

  • STOMP (Stopping over-medication of people with a learning disability, autism or both)
  • NICE guideline: Challenging behaviour and learning disabilities: prevention and interventions
  • Mental Capacity Act 2005 Code of Practice
  • GMC Good Practice in prescribing and managing medicines and devices
  • Royal College of Psychiatrists guidance on psychotropic drug prescribing for people with intellectual disability

 

 

Question 7: You receive a referral for a young woman with autism and a learning disability whose self-injury has increased. Her care home asks for medication. What is your approach?

Clinical Scenario question  ·  Clinical Scenario

 

What the interview panel is assessing

The panel wants to hear that you see behaviours that challenge as communication and that you look for causes before prescribing. They are listening for functional assessment, positive behaviour support, physical health, and a proportionate, safe role for medication.

 

Model answer

My starting point is that self-injury is telling us something, and my job is to help work out what before reaching for a prescription.

I'd begin with a thorough history from the home staff and her family. When did it increase? What does it look like? Is she hitting her head, biting her hand, picking her skin? Where, when and with whom does it happen, and what happens straight afterwards? I'd ask for ABC charts if they're not already in place, and look at any recent changes: new staff, a housemate moving in, a change in day activities, a missed family visit.

Head-hitting in particular makes me think about pain, so I'd want a physical review: ears, teeth, headaches, constipation, reflux, menstrual problems, urinary infections and seizures. I'd check her medication for side effects too. I'd also screen for mental illness, because self-injury can increase with depression or anxiety, and autistic people often find changes in routine and sensory overload really distressing.

At the same time I'd look at immediate risk. If she's injuring her head or eyes I'd want a plan to reduce harm now, agreed with the home and the team, avoiding unnecessary restriction.

Then I'd bring in the MDT. Our behaviour specialist or psychologist would lead a functional assessment and work with the home on a positive behaviour support plan. That means changing the environment, teaching other ways to communicate and having a clear, calm response when she's distressed. Speech and language therapy and occupational therapy might look at communication and sensory needs.

I wouldn't rule medication out entirely. If there's a treatable mental illness, or the risk is high and other approaches aren't enough on their own, a time-limited trial might be appropriate, with clear goals, monitoring and a review date. But it would be alongside behavioural support, never instead of it, and I'd discuss it with my consultant and with her or her family.

 

Why this answer works

The answer frames self-injury as communication, uses functional assessment, prioritises physical causes and immediate safety, and describes a proper positive behaviour support pathway. It places medication accurately as a possible, time-limited adjunct consistent with NICE and STOMP.

 

Key points to include

  • Behaviour as communication; look for function and triggers
  • Physical causes, especially pain, and medication side effects
  • Screen for mental illness, including anxiety and depression
  • Immediate harm-reduction plan with least restriction
  • Functional assessment and positive behaviour support led by the MDT
  • Medication only as a reviewed, time-limited adjunct where indicated

 

Common mistakes to avoid

  • Agreeing to prescribe straight away because the home has asked
  • Ignoring physical pain as a cause
  • Using restriction without considering least restrictive options
  • Forgetting the autistic person's sensory and routine needs

 

NHS values and standards

Compassion; Respect and dignity; Improving lives; GMC Good Medical Practice

 

Further reading

  • NICE guideline: Challenging behaviour and learning disabilities: prevention and interventions
  • STOMP (Stopping over-medication of people with a learning disability, autism or both)
  • Positive Behaviour Support Competence Framework
  • Restraint Reduction Network Training Standards
  • NICE guideline: Autism spectrum disorder in adults: diagnosis and management

 

 

Question 8: How do you keep your knowledge up to date in learning disability psychiatry, and how does that feed into revalidation?

Professional Development question  ·  Professional Development

 

What the interview panel is assessing

The panel is checking that you take ownership of your learning and understand the GMC's revalidation requirements. They want specific, relevant activities linked to the specialty rather than a vague list of courses.

 

Model answer

I try to make my learning match the patients I'm actually seeing, rather than collecting certificates.

Day to day, I use case-based learning. If I see something unfamiliar, like a rare genetic syndrome with a particular behavioural profile, I'll read up on it that week and bring it to our team's case discussion. I attend our local academic programme and the Faculty of Psychiatry of Intellectual Disability events when I can, and I keep an eye on new NICE guidance and the yearly LeDeR reports, because they tell us very directly where people are being let down.

I've completed the Oliver McGowan Mandatory Training on Learning Disability and Autism, and it was genuinely useful. Hearing directly from people with lived experience changes how you think in a way a textbook doesn't. I also do regular reflective practice. After a difficult case, like a placement breakdown or an admission I wasn't sure about, I'll write a short reflection on what I'd do differently.

For revalidation, I keep my portfolio organised around the GMC's requirements: continuing professional development, quality improvement activity, significant events, feedback from colleagues and patients, and compliments and complaints. In this specialty, getting meaningful patient feedback takes some thought, so I've used easy-read feedback forms and asked families and carers too. I'm also involved in a prescribing audit linked to STOMP, which counts as quality improvement.

I use my appraisal to set a personal development plan. At the moment my goals include strengthening my skills in autism diagnostic assessment and developing my understanding of the Mental Health Act reforms as they come into force. I find supervision with my consultant is where a lot of real learning happens, so I protect that time.

 

Why this answer works

The answer links learning to real clinical work and names specialty-relevant sources such as LeDeR, NICE and the Oliver McGowan training. It shows clear understanding of revalidation and appraisal and gives sensible adaptations, such as easy-read patient feedback.

 

Key points to include

  • Case-based, specialty-relevant learning
  • Awareness of LeDeR, NICE and RCPsych faculty resources
  • Oliver McGowan Mandatory Training and learning from lived experience
  • Understanding of GMC revalidation and annual appraisal
  • Adapting patient feedback to be accessible
  • A clear personal development plan

 

Common mistakes to avoid

  • Listing courses with no link to practice
  • Not knowing the elements of revalidation
  • Forgetting how to gather feedback from people with communication needs
  • Having no specific development goals

 

NHS values and standards

Commitment to quality of care; Improving lives; GMC Good Medical Practice: developing and maintaining your professional performance

 

Further reading

  • GMC Good Medical Practice
  • GMC guidance on supporting information for appraisal and revalidation
  • Oliver McGowan Mandatory Training on Learning Disability and Autism
  • Royal College of Psychiatrists CPD policy
  • LeDeR annual reports

 

 

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To prepare for a learning disability psychiatry NHS interview, expect questions on diagnostic overshadowing, assessing mental illness in people who communicate without many words, behaviours that challenge and positive behaviour support, STOMP and psychotropic prescribing, epilepsy, autism, the Mental Capacity Act and keeping people out of hospital through Care (Education) and Treatment Reviews. Build short spoken answers around real cases from your practice, and know the GMC's Good Medical Practice, the NHS values, LeDeR and Building the Right Support before you walk in.

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