<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(1)</volume><submitter>Birch N</submitter><funding>Rex Bionics Plc</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>The RAPPER II study investigates the feasibility, safety and acceptability of using the REX self-stabilising robotic exoskeleton in people with spinal cord injury (SCI) who are obligatory wheelchair users. Feasibility is assessed by the completion of transfer into the REX device, competency in achieving autonomous control and completion of upper body exercise in an upright position in the REX device. Safety is measured by the occurrence of serious adverse events. Device acceptability is assessed with a user questionnaire.&lt;h4>Methods&lt;/h4>RAPPER II is a prospective, multi-centre, open label, non-randomised, non-comparative cohort study in people with SCI recruited from neurological rehabilitation centres in the United Kingdom, Australia and New Zealand. This is the planned</pubmed_abstract><journal>Journal of neuroengineering and rehabilitation</journal><pagination>60</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5477376</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Results of the first interim analysis of the RAPPER II trial in patients with spinal cord injury: ambulation and functional exercise programs in the REX powered walking aid.</pubmed_title><pmcid>PMC5477376</pmcid><pubmed_authors>Priestley T</pubmed_authors><pubmed_authors>Birch N</pubmed_authors><pubmed_authors>Heywood C</pubmed_authors><pubmed_authors>Nunn A</pubmed_authors><pubmed_authors>Signal N</pubmed_authors><pubmed_authors>Gall A</pubmed_authors><pubmed_authors>Graham J</pubmed_authors><pubmed_authors>Sakel M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Results of the first interim analysis of the RAPPER II trial in patients with spinal cord injury: ambulation and functional exercise programs in the REX powered walking aid.</name><description>&lt;h4>Background&lt;/h4>The RAPPER II study investigates the feasibility, safety and acceptability of using the REX self-stabilising robotic exoskeleton in people with spinal cord injury (SCI) who are obligatory wheelchair users. Feasibility is assessed by the completion of transfer into the REX device, competency in achieving autonomous control and completion of upper body exercise in an upright position in the REX device. Safety is measured by the occurrence of serious adverse events. Device acceptability is assessed with a user questionnaire.&lt;h4>Methods&lt;/h4>RAPPER II is a prospective, multi-centre, open label, non-randomised, non-comparative cohort study in people with SCI recruited from neurological rehabilitation centres in the United Kingdom, Australia and New Zealand. This is the planned</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Jun</publication><modification>2025-04-25T17:54:11.407Z</modification><creation>2019-03-27T02:48:01Z</creation></dates><accession>S-EPMC5477376</accession><cross_references><pubmed>28629390</pubmed><doi>10.1186/s12984-017-0274-6</doi></cross_references></HashMap>