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A blended eHealth intervention for insomnia following acquired brain injury: a randomised controlled trial

The high prevalence and severe consequences of poor sleep following acquired brain injury emphasises the need for an effective treatment. However, treatment studies are scarce. The present study evaluates the efficacy of blended online cognitive behavioural therapy for insomnia (eCBT‐I) developed sp...

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Autores principales: Ford, Marthe E., Geurtsen, Gert J., Groet, Erny, Rambaran Mishre, Radha D., Van Bennekom, Coen A. M., Van Someren, Eus J. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078387/
https://www.ncbi.nlm.nih.gov/pubmed/35641443
http://dx.doi.org/10.1111/jsr.13629
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author Ford, Marthe E.
Geurtsen, Gert J.
Groet, Erny
Rambaran Mishre, Radha D.
Van Bennekom, Coen A. M.
Van Someren, Eus J. W.
author_facet Ford, Marthe E.
Geurtsen, Gert J.
Groet, Erny
Rambaran Mishre, Radha D.
Van Bennekom, Coen A. M.
Van Someren, Eus J. W.
author_sort Ford, Marthe E.
collection PubMed
description The high prevalence and severe consequences of poor sleep following acquired brain injury emphasises the need for an effective treatment. However, treatment studies are scarce. The present study evaluates the efficacy of blended online cognitive behavioural therapy for insomnia (eCBT‐I) developed specifically for people with acquired brain injury. In a multicentre prospective, open‐label, blinded end‐point randomised clinical trial, 52 participants with insomnia and a history of a stroke or traumatic brain injury were randomised to 6 weeks of guided eCBT‐I or treatment as usual, with a 6‐week follow‐up. The primary outcome measure was the change in insomnia severity between baseline and after treatment, measured with the Insomnia Severity Index. Results showed that insomnia severity improved significantly more with eCBT‐I than with treatment as usual compared to baseline, both at post‐treatment (mean [SEM] 4.0 [1.3] insomnia severity index points stronger decrease, d = 0.96, p < 0.003) and at follow‐up (mean [SEM] 3.2 [1.5] insomnia severity index points, d = −0.78, p < 0.03). In conclusion, our randomised clinical trial shows that blended CBT is an effective treatment for insomnia, and feasible for people with acquired brain injury, regardless of cognitive and psychiatric complaints. Online treatment has major advantages in terms of availability and cost and may contribute to the successful implementation of insomnia treatment for people with acquired brain injuries.
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spelling pubmed-100783872023-04-07 A blended eHealth intervention for insomnia following acquired brain injury: a randomised controlled trial Ford, Marthe E. Geurtsen, Gert J. Groet, Erny Rambaran Mishre, Radha D. Van Bennekom, Coen A. M. Van Someren, Eus J. W. J Sleep Res Poor Sleep and Insomnia The high prevalence and severe consequences of poor sleep following acquired brain injury emphasises the need for an effective treatment. However, treatment studies are scarce. The present study evaluates the efficacy of blended online cognitive behavioural therapy for insomnia (eCBT‐I) developed specifically for people with acquired brain injury. In a multicentre prospective, open‐label, blinded end‐point randomised clinical trial, 52 participants with insomnia and a history of a stroke or traumatic brain injury were randomised to 6 weeks of guided eCBT‐I or treatment as usual, with a 6‐week follow‐up. The primary outcome measure was the change in insomnia severity between baseline and after treatment, measured with the Insomnia Severity Index. Results showed that insomnia severity improved significantly more with eCBT‐I than with treatment as usual compared to baseline, both at post‐treatment (mean [SEM] 4.0 [1.3] insomnia severity index points stronger decrease, d = 0.96, p < 0.003) and at follow‐up (mean [SEM] 3.2 [1.5] insomnia severity index points, d = −0.78, p < 0.03). In conclusion, our randomised clinical trial shows that blended CBT is an effective treatment for insomnia, and feasible for people with acquired brain injury, regardless of cognitive and psychiatric complaints. Online treatment has major advantages in terms of availability and cost and may contribute to the successful implementation of insomnia treatment for people with acquired brain injuries. John Wiley and Sons Inc. 2022-05-31 2023-02 /pmc/articles/PMC10078387/ /pubmed/35641443 http://dx.doi.org/10.1111/jsr.13629 Text en © 2022 The Authors. Journal of Sleep Research published by John Wiley & Sons Ltd on behalf of European Sleep Research Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Poor Sleep and Insomnia
Ford, Marthe E.
Geurtsen, Gert J.
Groet, Erny
Rambaran Mishre, Radha D.
Van Bennekom, Coen A. M.
Van Someren, Eus J. W.
A blended eHealth intervention for insomnia following acquired brain injury: a randomised controlled trial
title A blended eHealth intervention for insomnia following acquired brain injury: a randomised controlled trial
title_full A blended eHealth intervention for insomnia following acquired brain injury: a randomised controlled trial
title_fullStr A blended eHealth intervention for insomnia following acquired brain injury: a randomised controlled trial
title_full_unstemmed A blended eHealth intervention for insomnia following acquired brain injury: a randomised controlled trial
title_short A blended eHealth intervention for insomnia following acquired brain injury: a randomised controlled trial
title_sort blended ehealth intervention for insomnia following acquired brain injury: a randomised controlled trial
topic Poor Sleep and Insomnia
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078387/
https://www.ncbi.nlm.nih.gov/pubmed/35641443
http://dx.doi.org/10.1111/jsr.13629
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