Randomized controlled trial of digital cognitive behavior therapy for prenatal insomnia symptoms: effects on postpartum insomnia and mental health.

Jennifer N Felder, Elissa S Epel, John Neuhaus, Andrew D Krystal, Aric A Prather
Author Information
  1. Jennifer N Felder: Osher Center for Integrative Health, University of California, San Francisco, CA, USA. ORCID
  2. Elissa S Epel: Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, CA, USA.
  3. John Neuhaus: Department of Epidemiology and Biostatistics, University of California, San Francisco, CA, USA.
  4. Andrew D Krystal: Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, CA, USA.
  5. Aric A Prather: Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, CA, USA.

Abstract

STUDY OBJECTIVES: To evaluate the effects of digital cognitive behavior therapy for insomnia (dCBT-I) delivered during pregnancy on subjective sleep outcomes, depressive symptoms, and anxiety symptoms through 6 months postpartum.
METHODS: People up to 28 weeks gestation (N = 208) with insomnia were randomized to 6 weekly sessions of dCBT-I or standard care. We report follow-up data at 3 and 6 months postpartum. The primary outcome was insomnia symptom severity. Secondary sleep outcomes included global sleep quality and insomnia caseness. Mental health outcomes included depressive and anxiety symptom severity. We evaluated between-condition differences in change from baseline for each postpartum timepoint and categorical outcomes.
RESULTS: dCBT-I participants did not experience significantly greater improvements in insomnia symptom severity relative to standard care participants, but they did experience higher rates of insomnia remission and lower rates of insomnia caseness at 6 months postpartum. dCBT-I participants experienced greater improvements in depressive symptom severity from baseline to both postpartum timepoints, and in anxiety symptom severity from baseline to 3 months postpartum. The proportion of participants with probable major depression at 3 months postpartum was significantly higher among standard care (18%) than dCBT-I (4%, p = 0.006) participants; this between-condition difference was pronounced among the subset (n = 143) with minimal depressive symptoms at baseline (18% vs 0%).
CONCLUSION: dCBT-I use during pregnancy leads to enduring benefits for postpartum insomnia remission. Findings provide strong preliminary evidence that dCBT-I use during pregnancy may prevent postpartum depression and anxiety, which is notable when considering the high frequency and importance of these problems.Clinical Trials: ClinicalTrials.gov, https://clinicaltrials.gov/ct2/show/NCT02805998, NCT02805998.

Keywords

Associated Data

ClinicalTrials.gov | NCT02805998

References

  1. Behav Sleep Med. 2021 May-Jun;19(3):395-406 [PMID: 32496138]
  2. Psychiatr Serv. 2008 Apr;59(4):429-32 [PMID: 18378843]
  3. Obstet Gynecol. 2017 Sep;130(3):573-581 [PMID: 28796676]
  4. Birth. 2006 Dec;33(4):323-31 [PMID: 17150072]
  5. Behav Sleep Med. 2021 Mar 15;:1-20 [PMID: 33719795]
  6. Br J Psychiatry. 1987 Jun;150:782-6 [PMID: 3651732]
  7. Sleep. 2012 Jun 01;35(6):769-81 [PMID: 22654196]
  8. J Sleep Res. 2018 Jun;27(3):e12643 [PMID: 29193493]
  9. Obstet Gynecol. 2005 Nov;106(5 Pt 1):1071-83 [PMID: 16260528]
  10. Sleep. 2021 Jun 11;44(6): [PMID: 33837426]
  11. Obstet Gynecol. 2019 May;133(5):911-919 [PMID: 30969203]
  12. J Pediatr Health Care. 2014 Jul-Aug;28(4):313-21 [PMID: 24007974]
  13. JAMA. 2019 Feb 12;321(6):580-587 [PMID: 30747971]
  14. J Clin Psychiatry. 2017 Sep/Oct;78(8):1110-1116 [PMID: 28297589]
  15. Arch Intern Med. 2006 May 22;166(10):1092-7 [PMID: 16717171]
  16. J Clin Psychiatry. 2012 Dec;73(12):e1478-84 [PMID: 23290331]
  17. JAMA Psychiatry. 2020 May 1;77(5):484-492 [PMID: 31968068]
  18. Psychiatry Res. 1989 May;28(2):193-213 [PMID: 2748771]
  19. Psychol Med. 2021 Jul 07;:1-11 [PMID: 34231450]
  20. J Affect Disord. 2019 Apr 1;248:155-165 [PMID: 30735852]
  21. Sleep Med Rev. 2018 Oct;41:87-100 [PMID: 29449122]
  22. Arch Womens Ment Health. 2006 Nov;9(6):309-15 [PMID: 17013761]
  23. Sleep. 2015 Aug 01;38(8):1237-45 [PMID: 25845691]
  24. JAMA. 2019 Feb 12;321(6):588-601 [PMID: 30747970]
  25. Lancet. 2014 Nov 15;384(9956):1800-19 [PMID: 25455250]
  26. JAMA Psychiatry. 2019 Jan 1;76(1):21-30 [PMID: 30264137]
  27. Ann Intern Med. 2016 Jul 19;165(2):125-33 [PMID: 27136449]
  28. Sleep. 2019 Oct 9;42(10): [PMID: 31535688]
  29. Arch Gen Psychiatry. 2010 Oct;67(10):1012-24 [PMID: 20921117]
  30. Sleep Med. 2020 Sep;73:82-92 [PMID: 32799029]
  31. Sleep. 2021 Jun 11;44(6): [PMID: 33830248]
  32. BMJ Open. 2014 Mar 18;4(3):e004183 [PMID: 24643168]
  33. Clin Child Fam Psychol Rev. 2011 Mar;14(1):1-27 [PMID: 21052833]
  34. J Sleep Res. 2020 Aug;29(4):e13018 [PMID: 32112507]
  35. Sleep Med. 2001 Jul;2(4):297-307 [PMID: 11438246]
  36. Matern Child Health J. 2015 Jun;19(6):1306-37 [PMID: 25452215]
  37. Ann Intern Med. 2015 Aug 4;163(3):191-204 [PMID: 26054060]

Grants

  1. K23 AT009896/NCCIH NIH HHS
  2. UL1 TR001872/NCATS NIH HHS
  3. R01 HL142051/NHLBI NIH HHS
  4. KL2 TR001870/NCATS NIH HHS
  5. T32 MH019391/NIMH NIH HHS

MeSH Term

Cognitive Behavioral Therapy
Female
Humans
Mental Health
Postpartum Period
Pregnancy
Sleep Initiation and Maintenance Disorders
Treatment Outcome

Word Cloud

Created with Highcharts 10.0.0insomniapostpartumdCBT-Ianxietymonthssymptomseverityparticipantspregnancyoutcomesdepressive6baselinecognitivebehaviortherapysleepsymptoms=standardcare3depressioneffectsdigitalincludedcasenesshealthbetween-conditionexperiencesignificantlygreaterimprovementshigherratesremissionamong18%useSTUDYOBJECTIVES:evaluatedeliveredsubjectiveMETHODS:People28weeksgestationN208randomizedweeklysessionsreportfollow-updataprimaryoutcomeSecondaryglobalqualityMentalevaluateddifferenceschangetimepointcategoricalRESULTS:relativelowerexperiencedtimepointsproportionprobablemajor4%p0006differencepronouncedsubsetn143minimalvs0%CONCLUSION:leadsenduringbenefitsFindingsprovidestrongpreliminaryevidencemaypreventnotableconsideringhighfrequencyimportanceproblemsClinicalTrials:ClinicalTrialsgovhttps://clinicaltrialsgov/ct2/show/NCT02805998NCT02805998Randomizedcontrolledtrialprenatalsymptoms:mental

Similar Articles

Cited By