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1000 Titel
  • Study protocol: multimodal physiotherapy as an add-on treatment to botulinum neurotoxin type A therapy for patients with cervical dystonia: DysPT-multi—a prospective, multicentre, single-blind, randomized, controlled study
1000 Autor/in
  1. Werner, Christian |
  2. Loudovici-Krug, Dana |
  3. Derlien, Steffen |
  4. Rakers, Florian |
  5. Smolenski, Ulrich C. |
  6. Lehmann, Thomas |
  7. Best, Norman |
  8. Günther, Albrecht |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-10-25
1000 Erschienen in
1000 Quellenangabe
  • 22(1):740
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13063-021-05705-8 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547107/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!Botulinum neurotoxin (BoNT) is currently the best therapeutic option in the treatment for cervical dystonia (CD). Additional treatments like physiotherapy (PT) may even improve the results of the BoNT injection with type A (BoNT-A), but there are no definite recommendations. In the last few years, some studies showed tendencies for PT as an adjuvant therapy to benefit. However, high-quality studies are required.!##!Methods!#!This study is a multicentre, randomized, single-blind, controlled trial to demonstrate the effectiveness of a multimodal PT program compared to a nonspecific cupping therapy, additionally to the BoNT-A therapy. Two hundred participants will be assigned into the multimodal PT plus BoNT intervention arm or the BoNT plus cupping arm using randomization. Primary endpoint is the total Score of Toronto Western Spasmodic Rating Scale (TWSTRS). Secondary endpoints are the mobility of the cervical spine (range of motion, ROM), the TWSTRS subscales, and the quality of life (measured by questionnaires: CDQ-24 and SF-36). Patients will be single-blind assessed every 3 months according to their BoNT injection treatment over a period of 9 months.!##!Discussion!#!The study aims to determine the effectiveness and therefore potential benefit of an additional multimodal physiotherapy for standardized treatment with BoNT-A in patients with CD, towards the BoNT-therapy alone. This largest randomized controlled trial in this field to date is intended to generate missing evidence for therapy guidelines.!##!Trial registration!#!The study was registered in the German Clinical Study Register before the start of the patient recruitment ( DRKS00020411 ; date: 21.01.2020).
1000 Sacherschließung
lokal Torticollis/diagnosis [MeSH]
lokal Study Protocol
lokal Humans [MeSH]
lokal Prospective Studies [MeSH]
lokal Treatment Outcome [MeSH]
lokal Multicenter Studies as Topic [MeSH]
lokal Physical Therapy Modalities [MeSH]
lokal Botulinum neurotoxin
lokal Randomized Controlled Trials as Topic [MeSH]
lokal Quality of Life [MeSH]
lokal Rehabilitation
lokal Cervical dystonia
lokal Botulinum Toxins, Type A/adverse effects [MeSH]
lokal Spasmodic torticollis
lokal Physiotherapy
lokal Single-Blind Method [MeSH]
lokal Neuromuscular Agents/adverse effects [MeSH]
lokal Treatment
lokal Torticollis/drug therapy [MeSH]
lokal Physical therapy
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/V2VybmVyLCBDaHJpc3RpYW4=|https://orcid.org/0000-0002-3538-234X|https://frl.publisso.de/adhoc/uri/RGVybGllbiwgU3RlZmZlbg==|https://frl.publisso.de/adhoc/uri/UmFrZXJzLCBGbG9yaWFu|https://frl.publisso.de/adhoc/uri/U21vbGVuc2tpLCBVbHJpY2ggQy4=|https://frl.publisso.de/adhoc/uri/TGVobWFubiwgVGhvbWFz|https://frl.publisso.de/adhoc/uri/QmVzdCwgTm9ybWFu|https://frl.publisso.de/adhoc/uri/R8O8bnRoZXIsIEFsYnJlY2h0
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1000 Erstellt am 2023-11-16T15:00:22.593+0100
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1000 Zuletzt bearbeitet 2023-12-01T02:30:15.273+0100
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