Sleeping for two: study protocol for a randomized controlled trial of cognitive behavioral therapy for insomnia in pregnant women

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dc.contributor.authorMacKinnon, Anna L.
dc.contributor.authorMadsen, Joshua W.
dc.contributor.authorDhillon, Ashley
dc.contributor.authorKeys, Elizabeth
dc.contributor.authorGiesbrecht, Gerald F.
dc.contributor.authorWilliamson, Tyler
dc.contributor.authorMetcalfe, Amy
dc.contributor.authorCampbell, Tavis
dc.contributor.authorMrklas, Kelly J.
dc.contributor.authorTomfohr-Madsen, Lianne
dc.date.accessioned2021-08-15T00:03:20Z
dc.date.available2021-08-15T00:03:20Z
dc.date.issued2021-08-12
dc.date.updated2021-08-15T00:03:20Z
dc.description.abstractAbstract Background Insomnia and sleep disturbances are common in pregnancy and have potentially significant consequences for both maternal and infant health. There is limited research examining the effectiveness of cognitive behavioral therapy for insomnia (CBT-I) during pregnancy. With increased distress and limited access to services during the COVID-19 pandemic, there is also an unprecedented need for telehealth delivery of treatment programs for pregnant women. The aims of this trial are to evaluate the impact of the Sleeping for Two adaptation of CBT-I in pregnancy (in-person or telehealth) versus treatment as usual (TAU) in reducing symptoms of insomnia (primary outcome), as well as increasing gestational length and reducing symptoms of depression (secondary outcomes). Methods A two-arm, single-blinded, parallel group randomized controlled trial (RCT) design with repeated measures will be used to evaluate the impact of CBT-I compared to TAU among a sample of 62 pregnant women, enrolled between 12 and 28 weeks of gestation, who self-identify as experiencing insomnia. Five weekly individual sessions of CBT-I will be delivered in person or via telehealth depending on physical distancing guidelines. Assessment of insomnia diagnosis by structured interview, self-reported insomnia symptom severity and sleep problems, and sleep quantity and quality as measured by a daily diary and actigraphy will occur at 12–28 weeks of pregnancy (T1), 1 week post-treatment (T2), and 6 months postpartum (T3). Discussion CBT-I delivered in pregnancy has the potential to reduce symptoms of insomnia and depression and could lead to reduced risk of preterm birth, all of which can minimize risk of negative maternal and child health and developmental consequences in the short (e.g., infant death) and long terms (e.g., developmental delays). This RCT builds on a successful open pilot trial conducted by our team and will provide further evaluation of a novel evidence-based treatment for pregnancy-related insomnia, which can be widely disseminated and used to treat individuals that are most in need of intervention. Findings will enhance understanding of pregnancy-related sleep problems, as well as means by which to improve the health and sleep of mothers and their children. Trial registration ClinicalTrials.gov NCT03918057. Registered on 17 April 2019.
dc.identifier.citationTrials. 2021 Aug 12;22(1):532
dc.identifier.doihttps://doi.org/10.1186/s13063-021-05498-w
dc.identifier.urihttp://hdl.handle.net/1880/113738
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dc.titleSleeping for two: study protocol for a randomized controlled trial of cognitive behavioral therapy for insomnia in pregnant women
dc.typeJournal Article
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