{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,7]],"date-time":"2025-11-07T09:55:18Z","timestamp":1762509318958,"version":"3.41.2"},"reference-count":33,"publisher":"Wiley","issue":"10","license":[{"start":{"date-parts":[[2025,6,24]],"date-time":"2025-06-24T00:00:00Z","timestamp":1750723200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100000272","name":"National Institute for Health and Care Research","doi-asserted-by":"publisher","award":["16\/167\/123"],"award-info":[{"award-number":["16\/167\/123"]}],"id":[{"id":"10.13039\/501100000272","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["obgyn.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["BJOG"],"published-print":{"date-parts":[[2025,9]]},"abstract":"<jats:title>ABSTRACT<\/jats:title><jats:sec><jats:title>Objective<\/jats:title><jats:p>To compare childbirth satisfaction in women with chronic or gestational hypertension, randomised to \u2018planned early term birth at 38<jats:sup>+0\u20133<\/jats:sup> weeks' gestation\u2019 (intervention) or \u2018usual care at term\u2019 (control).<\/jats:p><\/jats:sec><jats:sec><jats:title>Design<\/jats:title><jats:p>Randomised trial.<\/jats:p><\/jats:sec><jats:sec><jats:title>Setting<\/jats:title><jats:p>Forty\u2010two consultant\u2010led maternity units, United Kingdom.<\/jats:p><\/jats:sec><jats:sec><jats:title>Population<\/jats:title><jats:p>357\/403 women randomised completed the Childbirth Experience Questionnaire (CEQ).<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Mixed\u2010methods analysis of the 22\u2010item CEQ, assessing: \u2018Own capacity\u2019, \u2018Professional support\u2019, \u2018Perceived safety\u2019 and \u2018Participation\u2019. Directed content analysis sorted free\u2010text comments into themes covered by the CEQ and two additional themes.<\/jats:p><\/jats:sec><jats:sec><jats:title>Main Outcome Measures<\/jats:title><jats:p>CEQ scores overall and by domain.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>In intervention (vs. control) groups, the CEQ was completed by 177\/202, 88.1% (vs. 180\/202, 89.1%) participants, and 378 free\u2010text comments were made by 93\/177, 52.5% (vs. 98\/180, 54.4%) participants. There was no significant difference in CEQ scores overall (3.1\u2009\u00b1\u20090.4 vs. 3.1\u2009\u00b1\u20090.4, respectively) or by domain (\u2018Own capacity\u2019 [2.8\u2009\u00b1\u20090.5 vs. 2.7\u2009\u00b1\u20090.5, respectively]; \u2018Professional support\u2019 [3.7\u2009\u00b1\u20090.5 vs. 3.7\u2009\u00b1\u20090.6, respectively]; \u2018Perceived safety\u2019 [3.2\u2009\u00b1\u20090.6 vs. 3.1\u2009\u00b1\u20090.6, respectively]; and \u2018Participation\u2019 [2.6\u2009\u00b1\u20090.7 vs. 2.7\u2009\u00b1\u20090.6]). Most comments were positive (222\/378, 58.7%), and about \u2018Relational care and care interactions\u2019 (CEQ \u2018Professional support\u2019). Neither the number nor positivity of comments appeared to differ between groups.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>For women with chronic or gestational hypertension who remain well at term, we found no difference in childbirth experience between women randomised to planned early term birth versus usual care at term. Shared decisions about timing of birth may be more influenced by differences in clinical outcomes and costs.<\/jats:p><\/jats:sec><jats:sec><jats:title>Trial Registration<\/jats:title><jats:p><jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/www.isrctn.com\/ISRCTN77258279\">ISRCTN<\/jats:ext-link>: 77258279<\/jats:p><\/jats:sec>","DOI":"10.1111\/1471-0528.18257","type":"journal-article","created":{"date-parts":[[2025,6,24]],"date-time":"2025-06-24T23:35:06Z","timestamp":1750808106000},"page":"1426-1437","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Women's Childbirth Experiences in the WILL Randomised Trial (When to Induce Labour to Limit Risk in Pregnancy Hypertension): A Mixed Methods Analysis"],"prefix":"10.1111","volume":"132","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2344-4347","authenticated-orcid":false,"given":"Sue","family":"Tohill","sequence":"first","affiliation":[{"name":"Maternity Services, Guy's and St Thomas' National Health Service (NHS) Foundation Trust  London UK"},{"name":"Birmingham Clinical Trials Unit University of Birmingham  Birmingham UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Katie","family":"Kirkham","sequence":"additional","affiliation":[{"name":"Birmingham Clinical Trials Unit University of Birmingham  Birmingham UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eleni","family":"Gkini","sequence":"additional","affiliation":[{"name":"Birmingham Clinical Trials Unit University of Birmingham  Birmingham UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Catherine A.","family":"Moakes","sequence":"additional","affiliation":[{"name":"Birmingham Clinical Trials Unit University of Birmingham  Birmingham UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7177-3471","authenticated-orcid":false,"given":"Sergio A.","family":"Silverio","sequence":"additional","affiliation":[{"name":"Department of Psychology, Institute of Population Health University of Liverpool  Liverpool UK"},{"name":"Department of Women &amp; 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