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Stabilising sleep for patients admitted at acute crisis to a psychiatric hospital (OWLS): an assessor-blind pilot randomised controlled trial.
Sheaves, Bryony; Freeman, Daniel; Isham, Louise; McInerney, Josephine; Nickless, Alecia; Yu, Ly-Mee; Rek, Stephanie; Bradley, Jonathan; Reeve, Sarah; Attard, Caroline; Espie, Colin A; Foster, Russell; Wirz-Justice, Anna; Chadwick, Eleanor; Barrera, Alvaro.
Afiliação
  • Sheaves B; Sleep & Circadian Neuroscience Institute (SCNi), Department of Psychiatry, Warneford Hospital, University of Oxford,Oxford, OX3 7JX,UK.
  • Freeman D; Sleep & Circadian Neuroscience Institute (SCNi), Department of Psychiatry, Warneford Hospital, University of Oxford,Oxford, OX3 7JX,UK.
  • Isham L; Sleep & Circadian Neuroscience Institute (SCNi), Department of Psychiatry, Warneford Hospital, University of Oxford,Oxford, OX3 7JX,UK.
  • McInerney J; Oxford Health NHS Foundation Trust, Warneford Hospital,Oxford, OX3 7JX,UK.
  • Nickless A; Primary Care Clinical Trials Unit, Nuffield Department of Primary Care Health Sciences,University of Oxford,Radcliffe Primary Care Building, Radcliffe Observatory Quarter, Woodstock Road, Oxford, OX2 6GG,UK.
  • Yu LM; Primary Care Clinical Trials Unit, Nuffield Department of Primary Care Health Sciences,University of Oxford,Radcliffe Primary Care Building, Radcliffe Observatory Quarter, Woodstock Road, Oxford, OX2 6GG,UK.
  • Rek S; Sleep & Circadian Neuroscience Institute (SCNi), Department of Psychiatry, Warneford Hospital, University of Oxford,Oxford, OX3 7JX,UK.
  • Bradley J; Sleep & Circadian Neuroscience Institute (SCNi), Department of Psychiatry, Warneford Hospital, University of Oxford,Oxford, OX3 7JX,UK.
  • Reeve S; Department of Psychiatry,Warneford Hospital, University of Oxford,Oxford, OX3 7JX,UK.
  • Attard C; Berkshire Healthcare NHS Foundation Trust, Prospect Park Hospital,Honey End Lane, Tilehurst, Reading, Berkshire, RG30 4EJ,UK.
  • Espie CA; Sleep & Circadian Neuroscience Institute (SCNi), Nuffield Department of Clinical Neurosciences, OMPI, Sir William Dunn School of Pathology, University of Oxford,South Parks Road, Oxford, OX1 3RE,UK.
  • Foster R; Sleep & Circadian Neuroscience Institute (SCNi), Nuffield Department of Clinical Neurosciences, OMPI, Sir William Dunn School of Pathology, University of Oxford,South Parks Road, Oxford, OX1 3RE,UK.
  • Wirz-Justice A; Centre for Chronobiology, Psychiatric Hospital, University of Basel,Wilhelm Klein Strasse 27, CH-4012 Basel,Switzerland.
  • Chadwick E; Department of Psychiatry,Warneford Hospital, University of Oxford,Oxford, OX3 7JX,UK.
  • Barrera A; Oxford Health NHS Foundation Trust, Warneford Hospital,Oxford,OX3 7JX,UK.
Psychol Med ; 48(10): 1694-1704, 2018 07.
Article em En | MEDLINE | ID: mdl-29108526
BACKGROUND: When patients are admitted onto psychiatric wards, sleep problems are highly prevalent. We carried out the first trial testing a psychological sleep treatment at acute admission (Oxford Ward sLeep Solution, OWLS). METHODS: This assessor-blind parallel-group pilot trial randomised patients to receive sleep treatment at acute crisis [STAC, plus standard care (SC)], or SC alone (1 : 1). STAC included cognitive-behavioural therapy (CBT) for insomnia, sleep monitoring and light/dark exposure for circadian entrainment, delivered over 2 weeks. Assessments took place at 0, 2, 4 and 12 weeks. Feasibility outcomes assessed recruitment, retention of participants and uptake of the therapy. Primary efficacy outcomes were the Insomnia Severity Index and Warwick-Edinburgh Mental Wellbeing Scale at week 2. Analyses were intention-to-treat, estimating treatment effect with 95% confidence intervals. RESULTS: Between October 2015 and July 2016, 40 participants were recruited (from 43 assessed eligible). All participants offered STAC completed treatment (mean sessions received = 8.6, s.d. = 1.5). All participants completed the primary end point. Compared with SC, STAC led to large effect size (ES) reductions in insomnia at week 2 (adjusted mean difference -4.6, 95% CI -7.7 to -1.4, ES -0.9), a small improvement in psychological wellbeing (adjusted mean difference 3.7, 95% CI -2.8 to 10.1, ES 0.3) and patients were discharged 8.5 days earlier. One patient in the STAC group had an adverse event, unrelated to participation. CONCLUSIONS: In this challenging environment for research, the trial was feasible. Therapy uptake was high. STAC may be a highly effective treatment for sleep disturbance on wards with potential wider benefits on wellbeing and admission length.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Diagnostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Diagnostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article