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        <identifier>oai:figshare.com:article/34023408</identifier>
        <datestamp>2026-09-29T11:14:24Z</datestamp>
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          <dc:title>Effects of a hybrid digital Cognitive Behavioural Therapy for Insomnia and Emotion Regulation in the workplace (SLEEP) : study protocol for a randomised waitlist-control trial</dc:title>
          <dc:creator>Talarrita Moukhtarian (24993304)</dc:creator>
          <dc:creator>K. Patel (17228620)</dc:creator>
          <dc:creator>Carla T. Toro (5648162)</dc:creator>
          <dc:creator>S. Russel (24993307)</dc:creator>
          <dc:creator>G. Daley (15368204)</dc:creator>
          <dc:creator>Lukasz Walasek (6407675)</dc:creator>
          <dc:creator>Nicole K. Y. Tang (9916701)</dc:creator>
          <dc:creator>Caroline Meyer (6817790)</dc:creator>
          <dc:subject>Cognitive therapy</dc:subject>
          <dc:subject>Insomnia -- Treatment</dc:subject>
          <dc:subject>Insomniacs</dc:subject>
          <dc:subject>Emotions</dc:subject>
          <dc:subject>Migrated from ePrints</dc:subject>
          <dc:description>Introduction: This trial tests the efficacy of implementing a hybrid digital cognitive behavioural therapy for insomnia (dCBT-I) and emotion regulation (ER) in the workplace. The study protocol follows on the SPIRIT (Standard Protocol Items for Randomized Trials) 2013 recommendations. Methods and analysis: Mixed methods evaluation with a two-arm randomised waitlist control design of a six weeks dCBT-I+ER intervention through self-guided online platform and four videoconferencing therapy sessions. A process evaluation will examine fidelity of delivery and experiences of the intervention. Primary outcomes are the Insomnia Severity Index (ISI), the Patient Health Questionnaire (PHQ-9) and the Generalised Anxiety Disorder (GAD-7). Secondary outcomes are job productivity, job satisfaction, well-being, quality of life, self-reported (sleep diary data) and objective (actigraphy) sleep parameters, and usage of online intervention platform. Assessments take place at baseline (T0), week-8 post-treatment (T1), and week-12 post-randomisation (T2). We will recruit 156 workers with sleep and emotion regulation problems ranging from subclinical to clinical levels not engaged in treatment at the time of the trial.</dc:description>
          <dc:date>2022-07-15T00:00:00Z</dc:date>
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          <dc:identifier>10.1136/bmjopen-2021-058062</dc:identifier>
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