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The standard therapy recommended for sleep disorders is cognitive behavioural therapy for insomnia (CBT-I). Many of its interventions are based on a regular sleep and wake rhythm, which is difficult to apply for shift workers. We have therefore developed a new therapy manual specifically for shift workers (CBT-I-S), which should be more applicable to their needs. In particular, all interventions that require regularity have been removed, and instead, interventions that address factors that proved to be relevant to sleep in our preliminary study have been integrated. We now want to test this manual for its effectiveness.<\/jats:p>\n              <\/jats:sec><jats:sec>\n                <jats:title>Methods<\/jats:title>\n                <jats:p>A randomised controlled trial with <jats:italic>N<\/jats:italic>\u2009=\u2009142 will be conducted to compare two conditions: the newly developed therapy manual will be carried out in the experimental group, while cognitive behavioural therapy for insomnia will be employed in the standard group. Both treatments will be conducted online via MS Teams in a group setting with seven sessions each. Data will be collected at three measurement points (pre, post, 6-month follow-up) and analysed using linear mixed models. The study will investigate whether the two treatments have led to significant improvements in total sleep time, sleep onset latency, subjective sleep quality and daytime sleepiness in shift workers. It will also examine whether the new therapy manual is superior to standard therapy in shift workers and whether these effects are stable.<\/jats:p>\n              <\/jats:sec><jats:sec>\n                <jats:title>Discussion<\/jats:title>\n                <jats:p>We assume that interventions designed to address depressive mood, anxiety, worry, rumination, dysfunctional thought patterns and attitudes towards sleep will also improve sleep. If this is indeed the case, these interventions could replace previous ones that require regularity. This could significantly improve the treatment of insomnia in shift workers.<\/jats:p>\n              <\/jats:sec><jats:sec>\n                <jats:title>Trial registration<\/jats:title>\n                <jats:p>German Clinical Trials Registry DRKS <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"https:\/\/drks.de\/register\/de\/trial\/DRKS00032086\/preview\">DRKS00032086<\/jats:ext-link>. Registered on August 16, 2023.<\/jats:p>\n              <\/jats:sec>","DOI":"10.1186\/s13063-024-08403-3","type":"journal-article","created":{"date-parts":[[2024,8,26]],"date-time":"2024-08-26T09:02:30Z","timestamp":1724662950000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":6,"title":["Efficacy study comparing a CBT-I developed for shift workers (CBT-I-S) to standard CBT-I (cognitive behavioural therapy for insomnia) on sleep onset latency, total sleep time, subjective sleep quality, and daytime sleepiness: study protocol for a parallel group randomised controlled trial with online therapy groups of seven sessions each"],"prefix":"10.1186","volume":"25","author":[{"given":"Tanja","family":"Gr\u00fcnberger","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christopher","family":"H\u00f6hn","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Manuel","family":"Schabus","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anton-Rupert","family":"Laireiter","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2024,8,26]]},"reference":[{"key":"8403_CR1","doi-asserted-by":"publisher","DOI":"10.1007\/978-3-662-49789-0","volume-title":"Schlafmedizin 1x1","author":"T Cr\u00f6nlein","year":"2017","unstructured":"Cr\u00f6nlein T, Galetke W, Young P. 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In addition to the detailed protocol, the application included the text of the informed consent of the participants. Approval was granted on 12 July 2002. An amendment was submitted on 21 October 2023 to approve the cancellation of the control group and the payment of 50 Euro per participant. Informed consent to participate will be obtained from all participants: As this is an online study, all the information required therefore is available on the study website []. Here you agree to participate with all rights and obligations. Only then you will have access to the pre-screening.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethics approval and consent to participate"}},{"value":"Not applicable.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Consent for publication"}},{"value":"CH has received funding from the Doctoral College \u201eImaging the Mind \u201c of the Austrian Science Fund (FWF; W1233-B). All other authors declare that neither they nor any of the other persons involved have any financial or other competing or conflicting interests.","order":4,"name":"Ethics","group":{"name":"EthicsHeading","label":"Competing interests"}}],"article-number":"562"}}