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Hypertension with unsatisfactory sleep health (HUSH): study protocol for a randomized controlled trial
BACKGROUND: Insomnia is common in primary care medical practices. Although behavioral treatments for insomnia are safe, efficacious, and recommended in practice guidelines, they are not widely-available, and their effects on comorbid medical conditions remain uncertain. We are conducting a pragmatic...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461741/ https://www.ncbi.nlm.nih.gov/pubmed/28587609 http://dx.doi.org/10.1186/s13063-017-2001-9 |
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author | Levenson, Jessica C. Rollman, Bruce L. Ritterband, Lee M. Strollo, Patrick J. Smith, Kenneth J. Yabes, Jonathan G. Moore, Charity G. Harvey, Allison G. Buysse, Daniel J. |
author_facet | Levenson, Jessica C. Rollman, Bruce L. Ritterband, Lee M. Strollo, Patrick J. Smith, Kenneth J. Yabes, Jonathan G. Moore, Charity G. Harvey, Allison G. Buysse, Daniel J. |
author_sort | Levenson, Jessica C. |
collection | PubMed |
description | BACKGROUND: Insomnia is common in primary care medical practices. Although behavioral treatments for insomnia are safe, efficacious, and recommended in practice guidelines, they are not widely-available, and their effects on comorbid medical conditions remain uncertain. We are conducting a pragmatic clinical trial to test the efficacy of two cognitive behavioral treatments for insomnia (Brief Behavioral Treatment for Insomnia (BBTI) and Sleep Healthy Using the Internet (SHUTi)) versus an enhanced usual care condition (EUC). METHODS/DESIGN: The study is a three-arm, parallel group, randomized controlled trial. Participants include 625 adults with hypertension and insomnia, recruited via electronic health records from primary care practices affiliated with a large academic medical center. After screening and baseline assessments, participants are randomized to treatment. BBTI is delivered individually with a live therapist via web-interface/telehealth sessions, while SHUTi is a self-guided, automated, interactive, web-based form of cognitive behavioral therapy for insomnia. Participants in EUC receive an individualized sleep report, educational resources, and an online educational video. Treatment outcomes are measured at 9 weeks, 6 months, and 12 months. The primary outcome is patient-reported sleep disturbances. Secondary outcomes include other self-reported sleep measures, home blood pressure, body mass index, quality of life, health functioning, healthcare utilization, and side effects. DISCUSSION: This randomized clinical trial compares two efficacious insomnia interventions to EUC, and provides a cost-effective and efficient examination of their similarities and differences. The pragmatic orientation of this trial may impact sleep treatment delivery in real world clinical settings and advance the dissemination and implementation of behavioral sleep interventions. TRIAL REGISTRATION: ClinicalTrials.gov (Identifier: NCT02508129; Date Registered: July 21, 2015). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-017-2001-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5461741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54617412017-06-07 Hypertension with unsatisfactory sleep health (HUSH): study protocol for a randomized controlled trial Levenson, Jessica C. Rollman, Bruce L. Ritterband, Lee M. Strollo, Patrick J. Smith, Kenneth J. Yabes, Jonathan G. Moore, Charity G. Harvey, Allison G. Buysse, Daniel J. Trials Study Protocol BACKGROUND: Insomnia is common in primary care medical practices. Although behavioral treatments for insomnia are safe, efficacious, and recommended in practice guidelines, they are not widely-available, and their effects on comorbid medical conditions remain uncertain. We are conducting a pragmatic clinical trial to test the efficacy of two cognitive behavioral treatments for insomnia (Brief Behavioral Treatment for Insomnia (BBTI) and Sleep Healthy Using the Internet (SHUTi)) versus an enhanced usual care condition (EUC). METHODS/DESIGN: The study is a three-arm, parallel group, randomized controlled trial. Participants include 625 adults with hypertension and insomnia, recruited via electronic health records from primary care practices affiliated with a large academic medical center. After screening and baseline assessments, participants are randomized to treatment. BBTI is delivered individually with a live therapist via web-interface/telehealth sessions, while SHUTi is a self-guided, automated, interactive, web-based form of cognitive behavioral therapy for insomnia. Participants in EUC receive an individualized sleep report, educational resources, and an online educational video. Treatment outcomes are measured at 9 weeks, 6 months, and 12 months. The primary outcome is patient-reported sleep disturbances. Secondary outcomes include other self-reported sleep measures, home blood pressure, body mass index, quality of life, health functioning, healthcare utilization, and side effects. DISCUSSION: This randomized clinical trial compares two efficacious insomnia interventions to EUC, and provides a cost-effective and efficient examination of their similarities and differences. The pragmatic orientation of this trial may impact sleep treatment delivery in real world clinical settings and advance the dissemination and implementation of behavioral sleep interventions. TRIAL REGISTRATION: ClinicalTrials.gov (Identifier: NCT02508129; Date Registered: July 21, 2015). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-017-2001-9) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-06 /pmc/articles/PMC5461741/ /pubmed/28587609 http://dx.doi.org/10.1186/s13063-017-2001-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Levenson, Jessica C. Rollman, Bruce L. Ritterband, Lee M. Strollo, Patrick J. Smith, Kenneth J. Yabes, Jonathan G. Moore, Charity G. Harvey, Allison G. Buysse, Daniel J. Hypertension with unsatisfactory sleep health (HUSH): study protocol for a randomized controlled trial |
title | Hypertension with unsatisfactory sleep health (HUSH): study protocol for a randomized controlled trial |
title_full | Hypertension with unsatisfactory sleep health (HUSH): study protocol for a randomized controlled trial |
title_fullStr | Hypertension with unsatisfactory sleep health (HUSH): study protocol for a randomized controlled trial |
title_full_unstemmed | Hypertension with unsatisfactory sleep health (HUSH): study protocol for a randomized controlled trial |
title_short | Hypertension with unsatisfactory sleep health (HUSH): study protocol for a randomized controlled trial |
title_sort | hypertension with unsatisfactory sleep health (hush): study protocol for a randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461741/ https://www.ncbi.nlm.nih.gov/pubmed/28587609 http://dx.doi.org/10.1186/s13063-017-2001-9 |
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