Barriers to cognitive behavioural therapy for insomnia (CBTi)

Barriers to embedding CBTi in primary care are three‑fold:6

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Treatment priorities6

GPs’ perception of the patient6

Lack of confidence or experience7

Lack of time or resources6

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Lack of knowledge or awareness6

Time constraints6

Unable to fully engage6

Waiting times and accessibility6

Pharmacological treatment

If CBTi is not sufficiently effectiveunavailable or inappropriate for your patient, it is recommended that patients and their treating physicians should come to a shared decision about whether or not medication should be initiated.5 Many patients with chronic insomnia may feel like they have already exhausted options for behavioural modification, whether or not formal CBTi has been undertaken, and thus would prefer medical prescription at this stage.10

Traditional hypnotics, such as benzodiazepines and Z‑drugs are effective for the short‑term treatment of insomnia (3-7 days), however are not recommended for the long‑term management of chronic insomnia due to side effects with prolonged use.2,5,11,12

Prolonged-release melatonin is indicated as monotherapy for those ≥55 years with persistent insomnia.13 The recommended initial duration of treatment is 3 weeks and if the patient responds well, to continue for a further 10 weeks only. The risks associated with melatonin treatment in the elderly (including falls and fractures) must be assessed and discussed with the patient.2

QUVIVIQ™ is a dual orexin receptor antagonist (DORA) licensed to treat chronic insomnia in the UK.

DORAs

The introduction of DORAs can be considered the most significant recent development in the pharmacological management of insomnia.5 QUVIVIQ™ works differently to other hypnotics, reducing overactive wake-signalling and allowing restorative sleep to occur without altering the proportion of sleep stages.11,15-20

QUVIVIQ™ is NICE-recommended for treating insomnia in adults with symptoms lasting for 3 nights or more per week for at least 3 months, and whose daytime functioning is considerably affected, only if:14

The length of treatment should be as short as possible. Treatment with daridorexant (QUVIVIQ™) should be assessed within 3 months of starting and should be stopped in people whose long-term insomnia has not responded adequately. If treatment is continued, assess whether it is still working at regular intervals.14

QUVIVIQ™ does not appear to precipitate withdrawal symptoms or rebound insomnia upon discontinuation in clinical trials with up to 12 months of continuous treatment.5,11,15

DORA: dual orexin receptor antagonist; Z-drugs: zopiclone and zolpidem

QUVIVIQ™ is indicated for the treatment of adult patients with insomnia characterised by symptoms present for at least 3 months and considerable impact on daytime functioning.15

This information is intended for UK healthcare professionals.

This medicine is subject to additional monitoring.

Adverse events must be reported. Healthcare professionals are asked to report any suspected adverse reactions via www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in Google Play or Apple App Store. Adverse events should also be reported to ds.safety.uk@idorsia.com

References

  1. Morin C M, Drake C L et al. Insomnia disorder. Nat Rev Dis Primers 2015;1:15026
  2. National Institute for Health and Care Excellence (NICE). Clinical knowledge summary. Insomnia. Scenario: managing long-term insomnia (more than 3 months duration), May 2025. Available at: cks.nice.org.uk. Accessed August 2025
  3. Walker J, Muench A et al. Cognitive behavioral therapy for insomnia (CBT-I): a primer. Klin Spec Psihol 2022;11(2):123-137
  4. Rossman J. Cognitive-behavioral therapy for insomnia: an effective and underutilized treatment for insomnia. Am J Lifestyle Med 2019;13(6):544-547
  5. Riemann D, Espie C A et al. The European Insomnia Guideline: an update on the diagnosis and treatment of insomnia 2023. J Sleep Res 2023;32(6):e14035
  6. Koffel E, Bramoweth A D, Ulmer C S. Increasing access to and utilization of cognitive behavioral therapy for insomnia (CBT-I): a narrative review. J Gen Intern Med 2018;33(6):955-962
  7. Davy Z, Middlemass J, Siriwardena A N. Patients’ and clinicians’ experiences and perceptions of the primary care management of insomnia: qualitative study. Health Expect 2015;18(5):1371-1383
  8. M3 Idorsia insomnia market research. May 2022 GP Omnibus results (N=1, 002 UK GPs; update 22 June 2022)
  9. Espie C A, Henry A L. Disseminating cognitive behavioural therapy (CBT) for insomnia at scale: capitalising on the potential of digital CBT to deliver clinical guideline care. J Sleep Res 2023;32(6):e14025
  10. O’Regan D, Garcia-Borreguero D et al. Mapping the insomnia patient journey in Europe and Canada. Front Public Health 2023;11:1233201
  11. Mignot E, Mayleben D et al. Safety and efficacy of daridorexant in patients with insomnia disorder: results from two multicentre, randomised, double-blind, placebo-controlled, phase 3 trials. Lancet Neurol 2022;21(2):125-139
  12. National Institute for Health and Care Excellence (NICE). Clinical knowledge summary. Insomnia. Scenario: managing short-term insomnia (less than 3 months duration), May 2025. Available at: cks.nice.org.uk. Accessed August 2025
  13. Prolonged-release melatonin Summary of Product Characteristics
  14. National Institute for Health and Care Excellence (NICE). Technology appraisal guidance 922. Daridorexant for treating long‑term insomnia, 18 October 2023. Available at: nice.org.uk. Accessed August 2025
  15. QUVIVIQ™ Idorsia Pharmaceuticals Ltd, Summary of Product Characteristics

© NICE 2023 Daridorexant for treating long-term insomnia. Available from www.nice.org.uk/guidance/ta922. All rights reserved. Subject to Notice of rights.

NICE guidance is prepared for the National Health Service in England. All NICE guidance is subject to regular review and may be updated or withdrawn. NICE accepts no responsibility for the use of its content in this product/ publication.

UK-DA-00656 | Date of preparation: September 2025

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