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Manual therapy as a prophylactic treatment for migraine: design of a randomized controlled trial
BACKGROUND: People with migraine often experience disability with serious consequences for their social life and work productivity. The pharmacological prophylactic management of migraine is effective in reducing migraine attacks. However, many people are reluctant to use daily prophylactic medicati...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6935086/ https://www.ncbi.nlm.nih.gov/pubmed/31881911 http://dx.doi.org/10.1186/s13063-019-3937-8 |
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author | Amons, Andreas Leonard Castien, Rene Franciscus van der Wouden, Johannes C. De Hertogh, Willem Dekker, Joost van der Horst, Henriëtte Eveline |
author_facet | Amons, Andreas Leonard Castien, Rene Franciscus van der Wouden, Johannes C. De Hertogh, Willem Dekker, Joost van der Horst, Henriëtte Eveline |
author_sort | Amons, Andreas Leonard |
collection | PubMed |
description | BACKGROUND: People with migraine often experience disability with serious consequences for their social life and work productivity. The pharmacological prophylactic management of migraine is effective in reducing migraine attacks. However, many people are reluctant to use daily prophylactic medication, leading to a demand for non-pharmacological treatment options. We present the design for and discuss the feasibility of a pragmatic, randomized controlled trial on the effectiveness of a multimodal manual therapy (MT) treatment compared to usual care by the general practitioner (GP) for the prophylactic treatment of migraine. METHODS: Eligible participants will be recruited in primary care using the International Classification of Headache Disorders III criteria for migraine of the International Headache Society. Participants will be randomized to either multimodal MT treatment or usual care provided by the GP. GPs will be asked to treat the usual care group according to the Dutch GP guideline for headache. The multimodal MT intervention will include manual pressure techniques, neck muscle-strength exercises and mobilization of the cervical and thoracic spine. The trial will consist of a 12-week treatment period and follow-up measurements at 12, 26 and 52 weeks. The primary outcome measure is the number of migraine days per 4 weeks, assessed with a headache diary. Secondary outcome measures are the number of migraine attacks, medication use, disability due to headache, headache intensity, number of participants reporting a 50% migraine reduction, measurement of cervical pressure pain thresholds, presence of allodynia, endurance of cervical flexor muscles, days of absence of work and global perceived effect. DISCUSSION: The results of the trial will show whether a multimodal MT intervention is an effective non-pharmacological treatment option for people with migraine. TRIAL REGISTRATION: Dutch Trial Register, NL7504. Registered on 7 February 2019. |
format | Online Article Text |
id | pubmed-6935086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69350862019-12-30 Manual therapy as a prophylactic treatment for migraine: design of a randomized controlled trial Amons, Andreas Leonard Castien, Rene Franciscus van der Wouden, Johannes C. De Hertogh, Willem Dekker, Joost van der Horst, Henriëtte Eveline Trials Study Protocol BACKGROUND: People with migraine often experience disability with serious consequences for their social life and work productivity. The pharmacological prophylactic management of migraine is effective in reducing migraine attacks. However, many people are reluctant to use daily prophylactic medication, leading to a demand for non-pharmacological treatment options. We present the design for and discuss the feasibility of a pragmatic, randomized controlled trial on the effectiveness of a multimodal manual therapy (MT) treatment compared to usual care by the general practitioner (GP) for the prophylactic treatment of migraine. METHODS: Eligible participants will be recruited in primary care using the International Classification of Headache Disorders III criteria for migraine of the International Headache Society. Participants will be randomized to either multimodal MT treatment or usual care provided by the GP. GPs will be asked to treat the usual care group according to the Dutch GP guideline for headache. The multimodal MT intervention will include manual pressure techniques, neck muscle-strength exercises and mobilization of the cervical and thoracic spine. The trial will consist of a 12-week treatment period and follow-up measurements at 12, 26 and 52 weeks. The primary outcome measure is the number of migraine days per 4 weeks, assessed with a headache diary. Secondary outcome measures are the number of migraine attacks, medication use, disability due to headache, headache intensity, number of participants reporting a 50% migraine reduction, measurement of cervical pressure pain thresholds, presence of allodynia, endurance of cervical flexor muscles, days of absence of work and global perceived effect. DISCUSSION: The results of the trial will show whether a multimodal MT intervention is an effective non-pharmacological treatment option for people with migraine. TRIAL REGISTRATION: Dutch Trial Register, NL7504. Registered on 7 February 2019. BioMed Central 2019-12-27 /pmc/articles/PMC6935086/ /pubmed/31881911 http://dx.doi.org/10.1186/s13063-019-3937-8 Text en © The Author(s). 2019 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 Amons, Andreas Leonard Castien, Rene Franciscus van der Wouden, Johannes C. De Hertogh, Willem Dekker, Joost van der Horst, Henriëtte Eveline Manual therapy as a prophylactic treatment for migraine: design of a randomized controlled trial |
title | Manual therapy as a prophylactic treatment for migraine: design of a randomized controlled trial |
title_full | Manual therapy as a prophylactic treatment for migraine: design of a randomized controlled trial |
title_fullStr | Manual therapy as a prophylactic treatment for migraine: design of a randomized controlled trial |
title_full_unstemmed | Manual therapy as a prophylactic treatment for migraine: design of a randomized controlled trial |
title_short | Manual therapy as a prophylactic treatment for migraine: design of a randomized controlled trial |
title_sort | manual therapy as a prophylactic treatment for migraine: design of a randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6935086/ https://www.ncbi.nlm.nih.gov/pubmed/31881911 http://dx.doi.org/10.1186/s13063-019-3937-8 |
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