We invite the contribution of trials that meet the following criteria:

• Minimum dataset of 20 patients
• Documented entry criteria
• Documented consent or waiver of consent following local Institutional Review Board-approved procedure
• Included participants were randomised to their respective groups
• Baseline assessment includes recording of a recognised impairment/ activity limitation measure, eg. Barthel Index, NEADL, FIM, FAM, Oxford, NIHSS, SSS or similar
• Documentation of onset to treatment time
• Clinical diagnosis of stroke
• Outcome(s) assessed using one or more recognised measure(s)
• Trial was conducted within the last 10 years