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1000 Titel
  • Goal attainment in mobility after acute rehabilitation of mobility-restricting paralysis syndromes with regard to the ambulatory therapeutic level of participation NeuroMoves
1000 Autor/in
  1. Hug, Andreas |
  2. Spingler, Tamara |
  3. Hensel, Cornelia |
  4. Fichtner, Stefan |
  5. Daniel, Tiziana |
  6. Heutehaus, Laura |
  7. Wensing, Michel |
  8. Rupp, Rüdiger |
  9. Weidner, Norbert |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-04-07
1000 Erschienen in
1000 Quellenangabe
  • 21(1):149
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s12883-021-02167-y |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025358/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!A central goal of rehabilitation in patients with paralysis syndromes after stroke or spinal cord injury (SCI) is to restore independent mobility as a pedestrian or wheelchair user. However, after acute rehabilitation, the mobility frequently deteriorates in the ambulatory setting, despite the delivery of rehabilitative interventions such as physical therapy or the prescription of assistive devices. The aim of the NeuroMoves study is to identify factors that are associated with changes of mobility in the ambulatory setting after acute inpatient rehabilitation, with a particular focus on participation according to the ICF (International Classification of Functioning, Disability and Health).!##!Methods!#!The NeuroMoves study is intended as a national multicenter observational cohort study with 9 clinical sites in Germany. A total of 500 patients with mobility-restricting paralysis syndromes (i.e. stroke or SCI) are to be recruited during acute inpatient rehabilitation prior to discharge to the ambulatory setting. Patients will have 8 months of follow-up in the ambulatory setting. Three study visits at the clinical sites (baseline, midterm, and final) are planned at 4-months intervals. The baseline visit is scheduled at the end of the acute inpatient rehabilitation. During the visits, demographical data, neurological, functional, quality of life, and implementation measures will be assessed. At baseline, each study participant receives an activity tracker (sensor for recording ambulatory mobility) along with a tablet computer for home use over the 8 months study duration. While mounted, the activity tracker records mobility data from which the daily distance covered by walking or wheelchair use can be calculated. Customized applications on the tablet computer remind the study participants to answer structured questionnaires about their health condition and treatment goals for physical therapy. Using the study participants' tablet, therapists will be asked to answer structured questionnaires concerning treatment goals and therapeutic measures they have applied. The primary analysis concerns the association between mobility (daily distance covered) and the degree of participation-oriented rehab interventions. Further exploratory analyses are planned.!##!Discussion!#!The findings could inform healthcare decision-making regarding ambulatory care in Germany focusing on mobility-promoting interventions for patients with mobility-restricting paralysis syndromes.!##!Study registration!#!German Clinical Trials Register, DRKS-ID: DRKS00020487 (18.02.2020).
1000 Sacherschließung
lokal Surveys and Questionnaires [MeSH]
lokal Patient Discharge [MeSH]
lokal Spinal cord injury
lokal Goals [MeSH]
lokal ICF
lokal Study Protocol
lokal Humans [MeSH]
lokal Syndrome [MeSH]
lokal Paralysis/rehabilitation [MeSH]
lokal Physical Therapy Modalities [MeSH]
lokal Cohort Studies [MeSH]
lokal Disabled Persons [MeSH]
lokal Stroke
lokal Self-Help Devices [MeSH]
lokal Quality of Life [MeSH]
lokal Germany [MeSH]
lokal Spinal Cord Injuries/rehabilitation [MeSH]
lokal Ambulatory care
lokal Mobility
lokal Assistive devices
lokal Movement disorders
lokal Participation
lokal Physical therapy
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-7764-1813|https://frl.publisso.de/adhoc/uri/U3BpbmdsZXIsIFRhbWFyYQ==|https://frl.publisso.de/adhoc/uri/SGVuc2VsLCBDb3JuZWxpYQ==|https://frl.publisso.de/adhoc/uri/RmljaHRuZXIsIFN0ZWZhbg==|https://frl.publisso.de/adhoc/uri/RGFuaWVsLCBUaXppYW5h|https://frl.publisso.de/adhoc/uri/SGV1dGVoYXVzLCBMYXVyYQ==|https://frl.publisso.de/adhoc/uri/V2Vuc2luZywgTWljaGVs|https://frl.publisso.de/adhoc/uri/UnVwcCwgUsO8ZGlnZXI=|https://frl.publisso.de/adhoc/uri/V2VpZG5lciwgTm9yYmVydA==
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