01Purpose and principlesWhat the treatment does and how it fits into care.
Start by calculating sleep opportunity and likely total sleep rather than asking only whether the child sleeps well. Record usual wake time, bedtime, lights out, estimated sleep onset, awakenings, final waking and naps on weekdays and weekends. Ask what happens at each transition and who must be present. Large weekend catch-up suggests insufficient weekday sleep; a child placed in bed far before biological sleep time may appear to have insomnia.
Behavioural insomnia includes sleep-onset-association and limit-setting patterns. A child who falls asleep only while fed, rocked or beside a caregiver may need the same conditions after normal night arousals. In a limit-setting pattern, inconsistent or unenforceable boundaries prolong bedtime. These descriptions guide support and are not judgments about parenting. Illness, housing, shift work, disability, sibling care and cultural routines determine what is feasible.
Circadian delay produces late sleep and late waking with relatively normal quality when allowed the preferred schedule. It becomes prominent in adolescence and differs from anxious lying awake throughout the night. Morning light, fixed wake time and a gradual phase advance are central; an abrupt very early bedtime often increases wakefulness. Specialist input is appropriate for severe delay, school absence or consideration of timed melatonin.
Parasomnias arise from transitions between sleep states. Confusional arousals, sleepwalking and night terrors usually occur from deep non-REM sleep in the first third or half of the night. The child appears distressed or active but is difficult to console and typically has no clear memory. Nightmares arise later from REM sleep, wake the child fully and are remembered. Sleep deprivation, fever, stress and irregular schedule increase parasomnias.
Obstructive sleep apnoea in children often presents with loud snoring, gasping, unusual sleep positions, sweating, mouth breathing, enuresis, morning headache, irritability or hyperactivity rather than reported sleepiness. Examine tonsils, nasal airway, craniofacial anatomy, growth and blood pressure and consider obesity, neuromuscular weakness and Down syndrome. Absence of obvious tonsillar enlargement does not exclude obstruction.
Restless legs syndrome causes an urge or unpleasant sensation in the legs during rest, worse in the evening and relieved by movement. Children may describe tickling, pain or a need to run, and younger children may simply leave bed repeatedly. Ask about iron-deficient diet, heavy menstrual bleeding, coeliac symptoms and family history. Check FBC and ferritin when the clinical pattern or iron risk supports it, then treat deficiency through paediatric guidance rather than empirically giving iron indefinitely.
A 2-week sleep diary is usually the most useful first investigation. It reveals variability, opportunity and the relation between intervention and outcome. Actigraphy can estimate rest–activity timing over longer periods in specialist circadian or insomnia assessment but cannot identify every sleep stage or replace respiratory studies. Polysomnography records sleep, breathing, oxygenation, carbon dioxide, cardiac and movement signals and is the reference standard for obstructive sleep apnoea.
Behavioural treatment works through predictable cues, appropriate timing and consistent responses. Agree one achievable change at a time. Positive routines pair calm repeated activities with sleep; bedtime fading builds rapid sleep onset; graduated checking increases intervals between brief reassuring checks; and consistent return-to-bed reduces rewarding nighttime interaction. The family should understand the plan, anticipate a temporary increase in protest and know when to pause for illness or distress.
Extinction-based approaches are not mandatory and must never mean locking a child alone, ignoring illness or withholding comfort. Some families prefer caregiver fading, where the adult gradually moves farther away, or a visual schedule and reward plan. For neurodivergent children use concrete language, sensory adjustment and slower change. Review barriers without blame, particularly when overcrowding, caregiver mental health or domestic risk affects implementation.
Medicine has a narrow role. Modified-release melatonin can be considered within its licensed neurodevelopmental indications after sleep-hygiene and behavioural measures have been insufficient, with specialist diagnosis, an explicit target and periodic reassessment. Product formulation and timing determine effect; an immediate-release preparation is not automatically equivalent to a prolonged-release tablet. Routine antihistamines, benzodiazepines, antipsychotics or clonidine are not treatments for uncomplicated childhood insomnia.
Key points
- First-line assessment is a sleep history plus a 2-week diary recording sleep opportunity, estimated sleep, awakenings, naps, events, caffeine, screens and daytime effects.
- Set one consistent wake time every day, provide age-appropriate sleep opportunity, use morning light and daytime activity, and build a predictable calm wind-down.
- For behavioural insomnia, first-line management is a collaboratively chosen routine plus behavioural strategy such as bedtime fading, graduated checking or consistent low-interaction return to bed.
- Bedtime fading starts near the time the child actually falls asleep, then advances earlier in 5–15-minute steps once sleep onset is reliably quick.
- Typical night terrors occur from deep sleep in the first part of the night with autonomic distress, poor responsiveness and no next-day memory; protect from injury and do not force awakening.
- Polysomnography is the reference-standard test for suspected obstructive sleep apnoea, but referral and local prioritisation depend on clinical severity and service pathway.
- Melatonin is not first-line for ordinary bedtime resistance. Consider it only after behavioural and environmental work when a specialist indication and product-specific plan are clear.
02Indications, selection and cautionsWho may benefit, who needs urgent treatment and important alternatives.
A late bedtime or early required waking limits duration, with weekend catch-up, irritability or sleepiness despite no primary inability to sleep.
The child requires a specific caregiver, feeding, movement or setting to fall asleep and seeks the same condition after normal arousals.
Bedtime requests, leaving the room and delayed settling persist where expectations are unclear, inconsistent or impossible for the household to maintain.
Sleep begins and ends late but is relatively normal on a preferred schedule, with difficulty advancing to school or family timing.
A first-half-of-night episode has autonomic arousal, confused behaviour, limited responsiveness and little or no recall the next morning.
Habitual snoring, gasping, pauses, restless sleep, mouth breathing and daytime behavioural or learning effects suggest sleep-disordered breathing.
Events are brief, highly stereotyped or clustered and may include focal posturing, rhythmic movement, tongue injury or postictal change.
An evening urge or unpleasant leg sensation appears at rest and improves temporarily with movement, often disrupting sleep onset.
03Assessment before treatmentTests and checks that guide safe selection.
Read from the initial assessment onwards. Tests may run in parallel in urgent care; first-line, preferred, confirmatory, definitive and gold-standard labels appear only when the chapter explicitly states them.
- 01
First-line: 2-week sleep diaryFirst stepFirst line - Why
- Quantify schedule, opportunity, latency, waking, naps, events, triggers and daytime function before and during intervention.
- Interpretation and limitations
- Look for variability, weekend catch-up, bedtime placed before physiological sleep and response to routine; estimates need not be minute-perfect.
- 02
Sleep and medical history with examination - Why
- Identify behavioural pattern, respiratory obstruction, restless legs, pain, mental health, medicine effects and environmental barriers.
- Interpretation and limitations
- Examine growth, BMI, tonsils, nasal airway, blood pressure and neurology according to findings; urgent features override routine diary completion.
- 03
Reference standard: polysomnography for obstructive sleep apnoeaReference standard - Why
- Measure sleep state, airflow, respiratory effort, gas exchange, heart rhythm and movements when sleep-disordered breathing is suspected.
- Interpretation and limitations
- Severity is interpreted with paediatric criteria and clinical risk; local services may use limited studies for triage, but oximetry alone can miss obstruction.
- 04
Caregiver event video - Why
- Capture timing, responsiveness, breathing, movement pattern and duration of a recurrent nocturnal event when safe.
- Interpretation and limitations
- Useful collateral for parasomnia versus seizure, but never delay emergency action or physically restrain the child to obtain a recording.
- 05
Actigraphy - Why
- Estimate longitudinal rest–activity timing and variability in specialist assessment of circadian disorder or persistent insomnia.
- Interpretation and limitations
- It infers sleep from movement and requires a concurrent diary; it does not diagnose respiratory events or reliably distinguish all sleep stages.
- 06
FBC and ferritin - Why
- Identify iron deficiency when restless legs features, restrictive diet, bleeding or another iron-risk history is present.
- Interpretation and limitations
- Interpret ferritin with inflammation and laboratory range; use paediatric iron guidance and investigate the cause rather than applying an unverified universal target.
- 07
Targeted EEG or video telemetry - Why
- Investigate stereotyped, focal, clustered or otherwise seizure-suggestive nocturnal events after neurological review.
- Interpretation and limitations
- Not indicated for typical parasomnia and a normal routine EEG does not exclude epilepsy; event capture may be required.
04Treatment approachPreparation, options, escalation and aftercare.
01AssessmentClassify before interveningFirst stepSleep timing, night events or daytime function concerns the family.+
- 1Screen for respiratory compromise, seizure, acute mental-health risk, overdose, regression and safeguarding or supervision danger.
- 2Take an age-appropriate sleep, health, medicine and environmental history and start a 2-week diary with wake time, naps and events.
- 3Classify behavioural, circadian, respiratory, movement, parasomnia or neurological pattern and investigate only what the clinical question requires.
02FoundationStabilise timing and cuesNo emergency or untreated medical cause prevents behavioural work.+
- 1Agree a consistent daily wake time, appropriate sleep opportunity, morning light and activity, and age-appropriate nap timing.
- 2Create a repeatable 20–30-minute low-stimulation wind-down and reduce bright screens and caffeine before bed.
- 3Treat pain, itch, cough, constipation, anxiety and medication timing and adapt the bedroom for sensory, temperature, light and safety needs.
03Behavioural treatmentChoose one feasible methodSleep-onset association or bedtime behaviour perpetuates difficulty.+
- 1For late sleep onset, set bedtime near actual sleep time and advance it by 5–15 minutes after several reliably quick nights.
- 2Choose graduated brief checks, caregiver fading or consistent low-interaction return to bed, explain each response and use positive reinforcement for achievable steps.
- 3EscalationReview the diary after about 2–4 weeks, troubleshoot feasibility and strengthen consistency before adding or escalating treatment.
04ParasomniaProtect, reassure and reduce triggersA typical confusional arousal, sleepwalking episode or night terror occurs.+
- 1Secure doors, windows, stairs and hazards; guide gently without force and avoid trying to wake the child fully during an episode.
- 2Increase sleep opportunity and regularity and address fever, stress, obstructive breathing or medicines that increase arousals.
- 3If episodes are predictably timed and frequent, consider scheduled awakening before the usual event; refer when onset age, persistence, injury or seizure features are atypical.
05Specialist escalationInvestigate respiratory or neurological diseaseEscalationRed flags or persistent severe impairment remains.+
- 1Refer habitual snoring with apnoeas or risk factors to paediatric respiratory or ENT services for appropriate sleep study and airway management.
- 2Refer seizure-suggestive events, narcolepsy features or atypical parasomnia to paediatric neurology or sleep medicine with diary and safe video when available.
- 3For refractory insomnia, reassess diagnosis and behavioural implementation before a specialist considers timed melatonin within a licensed or clearly governed indication.
06Medicine reviewUse melatonin only with explicit goalsA specialist starts modified-release melatonin after behavioural measures are insufficient.+
- 1Confirm the exact licensed indication, formulation, dose timing, food instructions, interactions and target such as latency or night waking.
- 2Continue the behavioural plan and monitor diary outcomes, daytime sedation, mood, seizures, growth and adherence during titration.
- 3Evaluate after at least 3 months and stop if there is no clinically relevant response; reassess the continuing need periodically, including supervised treatment interruption when appropriate.
05Regimens, contraindications and interactionsTreatment details and the circumstances that modify them.
Melatonin prolonged-release tablets, Slenyto
Licensed paediatric indications: start 2 mg once daily, 30–60 minutes before bedtime and with or after food. If response is inadequate, increase to 5 mg and then maximum 10 mg daily according to the SmPC and specialist review.Swallow whole; do not crush or substitute another release profile. Review somnolence, headache, mood or behavioural change and seizure control. Check hepatic or renal disease, pregnancy potential in adolescents, CYP1A2 interactions including fluvoxamine, and smoking exposure. Evaluate after at least 3 months and stop if no clinically relevant effect; review at least every 6 months.
06Complications, monitoring and follow-upAdverse effects, response and longer-term review.
- Use the same 2-week diary variables after each change: wake time, bedtime, sleep-onset estimate, awakenings, naps, event frequency and daytime function.
- Review after approximately 2–4 weeks of a behavioural plan to check consistency, feasibility, distress and whether the original sleep classification remains correct.
- For snoring or suspected obstruction, monitor breathing events, growth, blood pressure, behaviour and learning while awaiting specialist assessment and escalate deterioration.
- For parasomnias, record timing, duration, injury and stereotypy; reassess when the pattern changes, persists beyond the expected age or develops neurological features.
- When treating iron deficiency, repeat blood tests and clinical review according to the paediatric regimen and investigate ongoing dietary, gastrointestinal or menstrual loss.
- With melatonin, monitor latency, total sleep, waking, daytime sedation, mood, seizure pattern, growth, interactions and adherence to the exact formulation.
- Evaluate melatonin after at least 3 months and discontinue when no clinically relevant benefit is demonstrated; after benefit is established, review the need at least every 6 months.
07Special situationsVariants, exceptions and circumstances that change the usual approach.
Wake time anchors the clock
A consistent morning wake time and light exposure usually shifts circadian timing more reliably than forcing an early bedtime.
Bedtime can be too early
Long wakefulness in bed strengthens frustration; bedtime fading first aligns bed with actual sleep, then advances gradually.
Night terror differs from nightmare
Night terrors arise early with poor responsiveness and amnesia, whereas nightmares occur later and are vividly recalled after full waking.
Melatonin timing matters
It is a chronobiotic as well as a sedative signal; indication, release profile, meal relation and clock time determine the effect.
08Common pitfallsFrequent interpretation and management errors.
- 01
Do not call every night waking behavioural before assessing breathing, pain, seizures, mental health and medicines.
- 02
Do not equate night terrors with nightmares or repeatedly force an aroused child awake.
- 03
Do not use normal overnight oximetry alone to exclude clinically suspected obstructive sleep apnoea.
- 04
Do not recommend punitive isolation, locked doors or an extinction method that prevents response to illness or danger.
- 05
Do not blame a family when housing, disability, caregiver mental health or shift work makes a standard routine unworkable.
- 06
Do not use sedating antihistamines, benzodiazepines, antipsychotics or clonidine routinely for uncomplicated insomnia.
- 07
Do not treat low ferritin indefinitely without a weight-appropriate regimen, monitoring and investigation of cause.
- 08
Do not start or continue melatonin without a defined target, behavioural plan, product-specific instructions and scheduled review.