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Home-based light therapy for fatigue following acquired brain injury: a pilot randomized controlled trial

BACKGROUND AND OBJECTIVES: Fatigue and sleep disturbance are debilitating problems following brain injury and there are no established treatments. Building on demonstrated efficacy of blue light delivered via a lightbox in reducing fatigue and daytime sleepiness after TBI, this study evaluated the e...

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Autores principales: Connolly, Laura J., Rajaratnam, Shantha M. W., Murray, Jade M., Spitz, Gershon, Lockley, Steven W., Ponsford, Jennie L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8256500/
https://www.ncbi.nlm.nih.gov/pubmed/34225698
http://dx.doi.org/10.1186/s12883-021-02292-8
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author Connolly, Laura J.
Rajaratnam, Shantha M. W.
Murray, Jade M.
Spitz, Gershon
Lockley, Steven W.
Ponsford, Jennie L.
author_facet Connolly, Laura J.
Rajaratnam, Shantha M. W.
Murray, Jade M.
Spitz, Gershon
Lockley, Steven W.
Ponsford, Jennie L.
author_sort Connolly, Laura J.
collection PubMed
description BACKGROUND AND OBJECTIVES: Fatigue and sleep disturbance are debilitating problems following brain injury and there are no established treatments. Building on demonstrated efficacy of blue light delivered via a lightbox in reducing fatigue and daytime sleepiness after TBI, this study evaluated the efficacy of a novel in-home light intervention in alleviating fatigue, sleep disturbance, daytime sleepiness and depressive symptoms, and in improving psychomotor vigilance and participation in daily productive activity, following injury METHODS: The impact of exposure to a dynamic light intervention (Treatment) was compared to usual lighting (Control) in a randomized within-subject, crossover trial. Outcomes were fatigue (primary outcome), daytime sleepiness, sleep disturbance, insomnia symptoms, psychomotor vigilance, mood and activity levels. Participants (N = 24, M ± SD(age) = 44.3 ± 11.4) had mild-severe TBI or stroke > 3 months previously, and self-reported fatigue (Fatigue Severity Scale ≥ 4). Following 2-week baseline, participants completed each condition for 2 months in counter-balanced order, with 1-month follow-up. Treatment comprised daytime blue-enriched white light (CCT > 5000 K) and blue-depleted light (< 3000 K) 3 h prior to sleep. RESULTS: Random-effects mixed-model analysis showed no significantly greater change in fatigue on the Brief Fatigue Inventory during Treatment, but a medium effect size of improvement (p = .33, d = -0.42). There were significantly greater decreases in sleep disturbance (p = .004), insomnia symptoms (p = .036), reaction time (p = .004) and improvements in productive activity (p = .005) at end of Treatment relative to Control, with large effect sizes (d > 0.80). Changes in other outcomes were non-significant. CONCLUSIONS: This pilot study provides preliminary support for in-home dynamic light therapy to address sleep-related symptoms in acquired brain injury. TRIAL REGISTRATION: This trial was registered with the Australian and New Zealand Clinical Trials Registry on 13 June 2017, www.anzctr.org.au, ACTRN12617000866303. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12883-021-02292-8.
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spelling pubmed-82565002021-07-06 Home-based light therapy for fatigue following acquired brain injury: a pilot randomized controlled trial Connolly, Laura J. Rajaratnam, Shantha M. W. Murray, Jade M. Spitz, Gershon Lockley, Steven W. Ponsford, Jennie L. BMC Neurol Research Article BACKGROUND AND OBJECTIVES: Fatigue and sleep disturbance are debilitating problems following brain injury and there are no established treatments. Building on demonstrated efficacy of blue light delivered via a lightbox in reducing fatigue and daytime sleepiness after TBI, this study evaluated the efficacy of a novel in-home light intervention in alleviating fatigue, sleep disturbance, daytime sleepiness and depressive symptoms, and in improving psychomotor vigilance and participation in daily productive activity, following injury METHODS: The impact of exposure to a dynamic light intervention (Treatment) was compared to usual lighting (Control) in a randomized within-subject, crossover trial. Outcomes were fatigue (primary outcome), daytime sleepiness, sleep disturbance, insomnia symptoms, psychomotor vigilance, mood and activity levels. Participants (N = 24, M ± SD(age) = 44.3 ± 11.4) had mild-severe TBI or stroke > 3 months previously, and self-reported fatigue (Fatigue Severity Scale ≥ 4). Following 2-week baseline, participants completed each condition for 2 months in counter-balanced order, with 1-month follow-up. Treatment comprised daytime blue-enriched white light (CCT > 5000 K) and blue-depleted light (< 3000 K) 3 h prior to sleep. RESULTS: Random-effects mixed-model analysis showed no significantly greater change in fatigue on the Brief Fatigue Inventory during Treatment, but a medium effect size of improvement (p = .33, d = -0.42). There were significantly greater decreases in sleep disturbance (p = .004), insomnia symptoms (p = .036), reaction time (p = .004) and improvements in productive activity (p = .005) at end of Treatment relative to Control, with large effect sizes (d > 0.80). Changes in other outcomes were non-significant. CONCLUSIONS: This pilot study provides preliminary support for in-home dynamic light therapy to address sleep-related symptoms in acquired brain injury. TRIAL REGISTRATION: This trial was registered with the Australian and New Zealand Clinical Trials Registry on 13 June 2017, www.anzctr.org.au, ACTRN12617000866303. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12883-021-02292-8. BioMed Central 2021-07-05 /pmc/articles/PMC8256500/ /pubmed/34225698 http://dx.doi.org/10.1186/s12883-021-02292-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Connolly, Laura J.
Rajaratnam, Shantha M. W.
Murray, Jade M.
Spitz, Gershon
Lockley, Steven W.
Ponsford, Jennie L.
Home-based light therapy for fatigue following acquired brain injury: a pilot randomized controlled trial
title Home-based light therapy for fatigue following acquired brain injury: a pilot randomized controlled trial
title_full Home-based light therapy for fatigue following acquired brain injury: a pilot randomized controlled trial
title_fullStr Home-based light therapy for fatigue following acquired brain injury: a pilot randomized controlled trial
title_full_unstemmed Home-based light therapy for fatigue following acquired brain injury: a pilot randomized controlled trial
title_short Home-based light therapy for fatigue following acquired brain injury: a pilot randomized controlled trial
title_sort home-based light therapy for fatigue following acquired brain injury: a pilot randomized controlled trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8256500/
https://www.ncbi.nlm.nih.gov/pubmed/34225698
http://dx.doi.org/10.1186/s12883-021-02292-8
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