Free DHA Psychiatry mock test
25 original exam-style questions from our Psychiatry bank, timed at the exam’s own pace, scored against the 65% DHA pass mark. They span 13 of the 13 blueprint domains, so you will see exactly where you are weakest - free, no sign-up.
Sit 25 original exam-style questions at real exam pace
These are 25 original questions taken from our Psychiatry bank, spread across 13 of the 13 domains of the published blueprint. You get 72 seconds per question, which is exactly the pace of the real PSY5961 exam (30 minutes for 25). At the end you will see which domains you are weakest in, and the full worked reasoning for every question.
- 25
- questions
- 30:00
- time limit
- 65%
- DHA pass mark
A short diagnostic cannot predict whether you will pass - only the real exam does that. It will show you, honestly, where you currently stand.
What the real Psychiatry licensing exam looks like
Candidates for a Psychiatry licence in the UAE sit a computer-based multiple-choice examination - DHA exam code PSY5961, delivered through Prometric for DHA, MOHAP and SHA, and through Pearson VUE for DOH Abu Dhabi. The DHA pass mark is 65% (DHA CBT Guideline, May 2026); other authorities set their own, so confirm yours before booking. The result is reported to you as pass or fail only - your score is never released.
Pass marks at a glance: DHA exam codes and pass marks for all written exams in one sourced table.
The paper is built to a published blueprint, which is why a domain-by-domain diagnostic is more useful than a raw percentage. Your questions above were drawn from across Consultation-Liaison (Psychosomatic) Psychiatry, Somatic Symptom & Neurocognitive Disorders, Child & Adolescent Psychiatry and Neurodevelopmental Disorders, Psychopharmacology & Somatic Therapies (ECT and Neuromodulation), Depressive, Bipolar & Related Disorders and 9 more - the same areas the real paper weights.
Before you can book the exam at all you need Dataflow primary source verification of your degree, licence and experience, which typically runs several weeks. Candidates routinely underestimate this and end up sitting the exam sooner after study than they planned. Check where you stand with our free eligibility checker or confirm whether your title even requires an exam using the Prometric exam checker.
You get three attempts in total across all UAE authorities - not three each - under the Unified Professional Qualification Requirements. At roughly AED 1,030 per attempt, plus the licensing delay each failure adds to your visa and start date, the cost of going in underprepared is not really the exam fee.
What is on the Psychiatry exam: the full blueprint
The published blueprint splits into 13 domains and 235 testable sub-topics. The diagnostic above samples across them, which is why its breakdown maps onto the structure the real paper is built from.
- Foundations: Neuroscience, Basic Psychology, Psychiatric Assessment & Classification~13%18 topics
est.; SCFHS Final blueprint gives 11% for Basic Sciences/Essential Topics plus 5% for Patient Evaluation/Descriptive Psychopathology
- Schizophrenia Spectrum & Other Psychotic Disorders~7%18 topics
est.; SCFHS Final blueprint 5%, DHA Exam Coverage names this domain explicitly
- Depressive, Bipolar & Related Disorders~8%18 topics
est.; SCFHS Final blueprint 5%, DHA Exam Coverage names this domain explicitly; commonly over-represented in licensure papers
- Anxiety, Obsessive-Compulsive & Related, Trauma- and Stressor-Related & Dissociative Disorders~8%18 topics
est.; SCFHS Final blueprint 5%, DHA Exam Coverage groups these together explicitly
- Personality, Impulse-Control, Feeding & Eating, Sleep-Wake, Sexual & Reproductive Psychiatry~6%18 topics
est.; SCFHS Final blueprint gives 5% to personality/trauma/dissociative, 5% to sleep-wake, 5% to sexuality/gender/reproductive; DHA names Personality Disorders explicitly
- Substance-Related & Addictive Disorders~9%18 topics
est.; SCFHS blueprint 10% in BOTH Part One and Final, DHA Exam Coverage names it explicitly - a high-yield domain
- Psychopharmacology & Somatic Therapies (ECT and Neuromodulation)~11%18 topics
est.; SCFHS Final blueprint 17% for Therapeutic Interventions shared with psychotherapy; DHA lists 'Basic Psychopharmacology / Physical Therapy (ECT and others)' explicitly
- Psychotherapy & Psychosocial Interventions~6%18 topics
est.; part of SCFHS 'Therapeutic Interventions' 17%; DHA lists 'Psychotherapy / Psychosocial Interventions' explicitly
- Consultation-Liaison (Psychosomatic) Psychiatry, Somatic Symptom & Neurocognitive Disorders~9%18 topics
est.; SCFHS Final blueprint 12% combined with geriatric; DHA lists 'Psychosomatic Medicine (Consultation-Liaison Psychiatry) / Somatic Symptom and Related Disorders' explicitly
- Child & Adolescent Psychiatry and Neurodevelopmental Disorders~9%18 topics
est.; SCFHS blueprint 10%, DHA Exam Coverage lists 'Child and Adolescent Psychiatry' explicitly
- Geriatric, Public/Community & Cross-Cultural Psychiatry~5%18 topics
est.; SCFHS pairs geriatric with C-L psychiatry; DHA Exam Coverage lists 'Public Psychiatry / Geriatric Psychiatry' explicitly
- Emergency Psychiatry, Risk Assessment & Crisis Management~5%18 topics
est.; SCFHS blueprint 5% in both Part One and Final; DHA Exam Coverage lists 'Emergency Psychiatry' explicitly
- Forensic Psychiatry, Mental Health Law, Ethics, Professionalism & Patient Safety~4%19 topics
est.; SCFHS notes ethics, professionalism and patient safety are embedded across domains; DHA Exam Coverage lists 'Forensic Psychiatry' and 'Patient Safety & Professionalism and Ethics' as separate explicit bullets, and this is the ORAL exam's graded third pillar
- Questions
- ~150 (DHA Specialist Psychiatry = 150 VERIFIED; QCHP specialty paper = 150; MOHAP = 150; OMSB written ~100; DOH ~100-150 unverified). DHA Consultant Psychiatry has NO MCQ paper - it is an oral assessment of not less than 5 clinical scenarios.
- Duration
- 3 hours (DHA Specialist Psychiatry = 3 hrs VERIFIED, inclusive of registration and process introduction; QCHP = 3 hrs; MOHAP = 3 hrs; NHRA = 3 hrs seating / 2.5 hrs testing; OMSB written = 2 hrs 30 min). Oral route: 20-30 minutes minimum, extendable (DHA); SCFHS consultant interview reported as 2 x 30 min sessions.
- Pass mark
- 65% (DHA Specialist Psychiatry PSY5961 - VERIFIED from the May 2026 CBT Guideline; note this differs from the 70% used for some other DHA specialty papers); 65% (QCHP specialty papers, OMSB written); 60% (MOHAP, NHRA physicians); 60-70% (DOH, unverified). For reference the SCFHS Saudi Board Psychiatry Final written exam uses 70% with a compensatory floor of 65%, and Part One uses 65% with a floor of 60%.
Single-best-answer MCQs, clinical-vignette dominant, computer-delivered, no negative marking; papers typically embed up to 10% unscored pretest/calibration items (explicitly stated in the SCFHS psychiatry blueprints). DHA exam code for Specialist Psychiatry is PSY5961, fee USD 280. Delivery: DHA / MOHAP / QCHP / NHRA / SCFHS via Prometric; DOH Abu Dhabi via Pearson VUE; OMSB via Pearson Professional Assessments (previously Prometric) plus an in-person viva in Muscat. DHA releases PASS/FAIL only in Sheryan and does not share the numeric score. An Eligibility ID must be generated by the authority (Sheryan for DHA, the NHRA online system for Bahrain, Mumaris+ for SCFHS) before booking, and DataFlow primary source verification is mandatory for QCHP from 01 Jan 2026. Attempts: DHA three; MOHAP three; NHRA four consecutive within three years. DHA's published reference list for Specialist Psychiatry is Kaplan and Sadock's Comprehensive Textbook of Psychiatry (latest edition), the New Oxford Textbook of Psychiatry (Gelder, Andreasen, Lopez-Ibor, Geddes), Essentials of Patient Safety (SCHS) and the SCFHS Professionalism and Ethics Handbook for Residents - write items to DSM-5-TR nomenclature and to those references. Domain weights below are anchored to the official SCFHS Saudi Board Psychiatry Final Examination blueprint and the DHA Exam Coverage bullets.
A worked Psychiatry exam question
Every question in the diagnostic and in the paid bank is written to this standard: a clinical stem, four plausible options and the reasoning for the answer, with its source.
Consultation-Liaison (Psychosomatic) Psychiatry, Somatic Symptom & Neurocognitive Disorders
A delirious postoperative patient with fluctuating cognition is refusing an urgently needed blood transfusion at 2 a.m. He had agreed to it four hours earlier when lucid. Which is the most appropriate action?
- AAccept the refusal as a valid advance decision
- BDocument that he lacks capacity at this moment because of delirium and, where the intervention is urgent and life-saving, proceed in his best interests, taking account of his previously expressed wishesCorrect
- CWait until the delirium resolves regardless of the urgency
- DSedate him covertly and record that consent was obtained
Why: Capacity is time-specific and can fluctuate, so a refusal made during an episode of impaired attention and awareness is not a capacitous decision, and for an urgent life-saving intervention the clinician acts in the patient's best interests while giving weight to his previously stated wishes. A refusal made without capacity cannot constitute a valid advance decision. Waiting could be fatal, and covert sedation with falsified documentation is both unlawful and a serious professional breach.
Source: UK Mental Capacity Act 2005 and Code of Practice; Appelbaum, New England Journal of Medicine (2007)
Psychiatry sample questions with answers
10 more original exam-style Psychiatry questions, worked in full. They are not real or recalled exam questions, and none of them is in the diagnostic above, so sit that first if you have not.
Question 1 · Psychopharmacology & Somatic Therapies (ECT and Neuromodulation)
A 38-year-old woman with refractory depression has failed fluoxetine 60 mg daily and is to be switched to phenelzine. Fluoxetine was stopped today. What is the minimum recommended interval before phenelzine can be started safely?
- A24 hours
- B1 week
- C2 weeks
- D5 weeks
Show answer and explanation
Correct answer: D. 5 weeks
Fluoxetine's active metabolite norfluoxetine has a half-life of one to two weeks, so a washout of at least five weeks is required before starting an MAOI to avoid fatal serotonin syndrome. Two weeks is the standard washout for most other SSRIs and SNRIs, and 24 hours or one week is grossly inadequate for fluoxetine.
Reference: Fluoxetine and phenelzine Summaries of Product Characteristics (EMA/MHRA); Maudsley Prescribing Guidelines in Psychiatry, 14th edition, 2021
Question 2 · Consultation-Liaison (Psychosomatic) Psychiatry, Somatic Symptom & Neurocognitive Disorders
A 44-year-old man on thrice-weekly haemodialysis repeatedly leaves sessions early and exceeds fluid limits, presenting recurrently with pulmonary oedema. He says he feels trapped and hopeless and can see no future. Which is the most appropriate initial response from the liaison psychiatrist?
- AAssess for and treat depression, and explore the meaning of non-adherence with a collaborative behavioural plan agreed with the renal team
- BRecommend that the renal team declare him non-compliant and withdraw dialysis
- CAssess capacity and, if capacitous, take no further action
- DStart lithium to stabilise his mood and reduce impulsivity
Show answer and explanation
Correct answer: A. Assess for and treat depression, and explore the meaning of non-adherence with a collaborative behavioural plan agreed with the renal team
Depression is highly prevalent in end-stage renal disease and is an independent predictor of dialysis non-adherence, hospitalisation and mortality, so identifying and treating it while addressing the behaviour collaboratively is the correct first step. Withdrawing dialysis in response to non-adherence is neither clinically nor ethically justified at this stage. A capacity assessment alone abandons a treatable disorder, and lithium is hazardous and complex to dose in dialysis and is not indicated here.
Reference: Kimmel et al., Kidney International (2000); KDIGO and Renal Association guidance on psychosocial care in end-stage kidney disease
Question 3 · Depressive, Bipolar & Related Disorders
A 25-year-old man with bipolar I disorder relapses repeatedly after discharge. He lives with parents who are highly critical and over-involved, frequently arguing about his medication. He is adherent to lithium at therapeutic levels. Which psychosocial intervention has the strongest evidence for reducing relapse in this specific situation?
- AFamily-focused therapy
- BLong-term individual psychoanalytic psychotherapy
- CNon-directive supportive counselling for the patient alone
- DInterpersonal and social rhythm therapy for the parents
Show answer and explanation
Correct answer: A. Family-focused therapy
Family-focused therapy combines psychoeducation, communication enhancement training and problem-solving skills with the patient and relatives, and randomised trials show it reduces relapse and hospitalisation in bipolar disorder, especially in households with high expressed emotion (criticism, hostility and emotional over-involvement). Long-term psychoanalytic therapy and non-directive individual counselling lack comparable relapse-prevention evidence in bipolar disorder. Interpersonal and social rhythm therapy is an evidence-based bipolar treatment but is delivered to the patient to stabilise daily routines, not to the parents.
Reference: Miklowitz DJ et al., Family-focused treatment for bipolar disorder, Archives of General Psychiatry / JAMA Psychiatry meta-analysis 2021; CANMAT/ISBD Guidelines, 2018
Question 4 · Schizophrenia Spectrum & Other Psychotic Disorders
A 33-year-old woman admitted in catatonic stupor has been receiving lorazepam 6 mg daily for 48 hours with minimal benefit. She now has a temperature of 39.2°C, pulse 132/min, labile blood pressure, profuse diaphoresis, rigidity and creatine kinase of 4,200 U/L. She has received no antipsychotic. Which is the most appropriate definitive management?
- AUrgent electroconvulsive therapy alongside intensive supportive care and continued benzodiazepine
- BStart haloperidol to control the underlying psychosis
- CStart dantrolene and bromocriptine and discharge to the psychiatric ward
- DSwitch lorazepam to clonazepam and reassess in 72 hours
Show answer and explanation
Correct answer: A. Urgent electroconvulsive therapy alongside intensive supportive care and continued benzodiazepine
Fever, autonomic instability, rigidity and raised creatine kinase in a catatonic patient indicate malignant catatonia, a life-threatening emergency; when benzodiazepines fail, urgent bilateral ECT is the definitive treatment and should not be delayed. Antipsychotics, particularly high-potency agents such as haloperidol, can precipitate or worsen malignant catatonia and neuroleptic malignant syndrome. Dantrolene and bromocriptine target neuroleptic malignant syndrome and are adjunctive at best here, and simply changing benzodiazepine wastes critical time in a condition with high mortality if untreated.
Reference: Sienaert et al., Frontiers in Psychiatry (2014), clinical review of the treatment of catatonia; APA Practice Guideline for the Treatment of Patients with Schizophrenia, 3rd edition (2020)
Question 5 · Psychotherapy & Psychosocial Interventions
A community mental health service is deciding which patients to allocate to its assertive community treatment team. Which patient is most likely to benefit from this model?
- AA woman with a first episode of moderate depression who has attended every clinic appointment
- BA man with panic disorder who wishes to reduce his benzodiazepine use
- CA woman with generalised anxiety disorder awaiting CBT
- DA man with schizophrenia and cannabis use who has had five admissions in two years, disengages from clinic follow-up and is repeatedly homeless
Show answer and explanation
Correct answer: D. A man with schizophrenia and cannabis use who has had five admissions in two years, disengages from clinic follow-up and is repeatedly homeless
Assertive community treatment, with its small shared caseloads, assertive outreach and in-vivo delivery, shows benefit mainly for patients with severe mental illness who have high service use and poor engagement, reducing admissions and improving housing stability and retention in care. Patients with common mental disorders who attend appointments reliably gain nothing from this resource-intensive model and are better served by standard outpatient or stepped care.
Reference: Marshall M, Lockwood A, Cochrane Database of Systematic Reviews (assertive community treatment for severe mental disorders), 2011; NICE CG178, 2014
Question 6 · Emergency Psychiatry, Risk Assessment & Crisis Management
A 52-year-old man with decompensated alcoholic cirrhosis, jaundice and a prolonged INR is admitted in alcohol withdrawal with tremor, sweating and a rising CIWA-Ar score. Which benzodiazepine regimen is most appropriate?
- AChlordiazepoxide in a high fixed-dose schedule
- BLong-acting diazepam at high dose to prevent seizures
- CLorazepam or oxazepam, cautiously titrated to symptoms
- DAvoid benzodiazepines entirely and use haloperidol as the primary agent
Show answer and explanation
Correct answer: C. Lorazepam or oxazepam, cautiously titrated to symptoms
Lorazepam and oxazepam undergo glucuronidation without hepatic oxidative metabolism and have no active metabolites, so they do not accumulate in significant liver impairment. Chlordiazepoxide and diazepam are long-acting oxidatively metabolised drugs that accumulate and can precipitate hepatic encephalopathy. Benzodiazepines remain the treatment of choice for withdrawal because they prevent seizures and delirium tremens; haloperidol lowers the seizure threshold and is only an adjunct for persistent hallucinations or agitation.
Reference: NICE CG100 (2010); American Society of Addiction Medicine Clinical Practice Guideline on Alcohol Withdrawal Management (2020)
Question 7 · Foundations: Neuroscience, Basic Psychology, Psychiatric Assessment & Classification
Which statement best characterises the Research Domain Criteria (RDoC) framework?
- AIt is a research framework organising study of psychopathology across functional domains and units of analysis, independent of DSM/ICD categories
- BIt is a replacement diagnostic manual intended for routine clinical coding and billing
- CIt defines new categorical disorders based on genome-wide association findings
- DIt abolishes dimensional measurement in favour of strictly categorical constructs
Show answer and explanation
Correct answer: A. It is a research framework organising study of psychopathology across functional domains and units of analysis, independent of DSM/ICD categories
RDoC, launched by the US National Institute of Mental Health, is explicitly a research framework that organises investigation around functional domains such as negative valence, positive valence, cognitive, social processes, arousal/regulatory and sensorimotor systems, each studied across units of analysis from genes and circuits to behaviour and self-report. It is deliberately not a clinical diagnostic system and is not used for coding or billing, does not define new categorical disorders, and is dimensional rather than categorical in its approach.
Reference: Insel et al., Research Domain Criteria (RDoC), Am J Psychiatry (2010); NIMH RDoC framework documentation
Question 8 · Substance-Related & Addictive Disorders
In the three-stage model of addiction (binge/intoxication, withdrawal/negative affect, preoccupation/anticipation), which neural substrate is most responsible for the dysphoria, anxiety and irritability that dominate the withdrawal/negative affect stage?
- ANigrostriatal dopaminergic projections to the putamen
- BIncreased glutamatergic drive from the dorsolateral prefrontal cortex to the hippocampus
- CCholinergic projections from the nucleus basalis of Meynert to the neocortex
- DRecruitment of corticotropin-releasing factor and dynorphin systems in the extended amygdala
Show answer and explanation
Correct answer: D. Recruitment of corticotropin-releasing factor and dynorphin systems in the extended amygdala
Koob and Volkow attribute the withdrawal/negative affect stage to 'anti-reward' recruitment of stress systems in the extended amygdala, principally corticotropin-releasing factor and dynorphin acting at kappa-opioid receptors, together with reduced accumbens dopamine. The preoccupation/anticipation stage is the prefrontal-cortical (executive/craving) stage, while nigrostriatal and basal-forebrain cholinergic systems mediate motor and attentional/memory functions rather than withdrawal dysphoria.
Reference: Koob GF, Volkow ND, Neurobiology of Addiction: A Neurocircuitry Analysis, Lancet Psychiatry, 2016
Question 9 · Child & Adolescent Psychiatry and Neurodevelopmental Disorders
A 4-year-old boy has had 12 hospital admissions for recurrent, unexplained hypoglycaemia and seizures. Investigations are always normal, episodes only ever occur when his mother is present, and she is unusually knowledgeable and comfortable on the ward. A nurse finds insulin in her handbag. Which is the most appropriate formulation and immediate action?
- ASomatic symptom disorder in the child; reassure and discharge
- BFactitious disorder imposed on another; ensure the child's immediate safety, involve child protection and separate the child from the suspected perpetrator pending investigation
- CMaternal generalised anxiety disorder; refer her for CBT and continue joint admissions
- DMalingering by the mother for financial gain; confront her in the ward round
Show answer and explanation
Correct answer: B. Factitious disorder imposed on another; ensure the child's immediate safety, involve child protection and separate the child from the suspected perpetrator pending investigation
Recurrent unexplained illness occurring only in a caregiver's presence, with normal investigations and physical evidence of induction, is factitious disorder imposed on another (medical child abuse) - a form of child abuse that carries substantial mortality. The priority is the child's immediate safety through child protection referral and separation pending multi-agency investigation, not immediate confrontation, which risks flight or escalation. Somatic symptom disorder and maternal anxiety do not explain injected insulin, and malingering requires an external incentive that is not the defining feature here.
Reference: American Psychiatric Association, DSM-5-TR (2022); Royal College of Paediatrics and Child Health, Perplexing Presentations and Fabricated or Induced Illness guidance (2021)
Question 10 · Anxiety, Obsessive-Compulsive & Related, Trauma- and Stressor-Related & Dissociative Disorders
The same 8-year-old boy has a positive throat culture for group A streptococcus and severe, functionally impairing obsessive-compulsive symptoms. What is the most appropriate initial management?
- AIntravenous immunoglobulin as first-line therapy for all such cases
- BIndefinite prophylactic penicillin for every child with abrupt-onset OCD, regardless of streptococcal status
- CTherapeutic plasma exchange before any psychiatric treatment
- DAntibiotic eradication of the confirmed streptococcal infection together with standard OCD treatment (CBT with exposure and response prevention, plus a low, slowly titrated SSRI if needed)
Show answer and explanation
Correct answer: D. Antibiotic eradication of the confirmed streptococcal infection together with standard OCD treatment (CBT with exposure and response prevention, plus a low, slowly titrated SSRI if needed)
Consensus treatment guidance is to treat the confirmed active streptococcal infection with an appropriate antibiotic while simultaneously delivering standard, evidence-based OCD care, namely CBT with exposure and response prevention and, for moderate-to-severe symptoms, an SSRI started at a low dose and titrated slowly because these children are prone to behavioural activation. Immunomodulatory treatments such as IVIG and plasma exchange are reserved for severe, refractory, clearly immune-mediated cases in specialist settings, not for routine first-line use. Long-term antibiotic prophylaxis is not recommended indiscriminately and lacks supporting evidence in the absence of documented recurrent streptococcal infection.
Reference: Thienemann et al., PANS/PANDAS Consensus Treatment Guidelines Part I-III, J Child Adolesc Psychopharmacol (2017); NICE CG31 (2005, reviewed)
How to use this diagnostic properly
- 1Sit it cold, once. Do not look anything up. A diagnostic you help yourself through tells you nothing. The number you get is only useful if it is honest.
- 2Read every rationale - especially the ones you got right. Getting a question right by elimination is not the same as knowing it. The worked reasoning is free above, whether or not you buy anything.
- 3Work weakest domain first. The breakdown orders your domains worst-first for exactly this reason. Studying what you are already good at feels productive and moves nothing.
- 4Re-sit under full exam conditions later. The real paper is far longer than this and stamina matters. Full-length timed papers are what the paid bank is for.