Review Article
Motor Training in Degenerative Spinocerebellar Disease: Ataxia-Specific Improvements by Intensive Physiotherapy and Exergames
Table 1
Overview of high-intensity training studies in degenerative ataxia.
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
SCA: spinocerebellar ataxia; FRDA: Friedreich’s ataxia; IDCA: idiopathic cerebellar ataxia; ADCA: autosomal dominant cerebellar ataxia of unknown type; SANDO: sensory ataxic neuropathy with dysarthria and ophthalmoparesis caused by mutations in the polymerase gamma gene; SN: sensory neuropathy with cerebellar degeneration; arCA: autosomal recessive cerebellar ataxia of unknown type; AOA2: ataxia with oculomotor apraxia type 2; SARA: scale for the assessment and rating of ataxia; ABC: activity-specific balance confidence scale; BBS: Berg balance score; GAS: goal attainment scaling [42]; DGI: dynamic Gait index; FIM: functional independence measure [38]; and FAC: functional ambulation categories. Evidence was graded according to the Oxford Center for Evidence Based Medicine (CEBM) classification. This table presents details of the first three clinical studies of motor rehabilitation in larger cohorts in degenerative spinocerebellar disease [34–36, 43]. |