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. 2015 Feb 12;2015(2):CD008349. doi: 10.1002/14651858.CD008349.pub3

Piron 2007

Methods RCT
Participants Study took place in Italy
38 participants: 25 intervention, 13 control
Inclusion criteria: mild‐intermediate arm motor impairment due to ischaemic stroke in the MCA territory within the past 3 months
Exclusion criteria: cognitive impairment, neglect, apraxia, aphasia interfering with comprehension
Mean (SD) age: intervention group 62 (9) years, control group 61 (7) years
66% male
Timing post stroke: intervention group mean (SD) 2.5 (1.5) months, control group 2.6 (1.6) months
Interventions Virtual reality intervention: magnetic receivers were positioned on the participant's arm. As the participant grasped and moved real objects, software created a virtual environment which displayed virtual handling and target objects, for example an envelope and a mailbox, a hammer and a nail, a glass and a carafe. While performing the virtual tasks such as putting the envelope in the mailbox the participant moves the real envelope and sees on screen the trajectory of the corresponding virtual objects toward the virtual mailbox. Participants could see not only their own movement but also the correct trajectory that they had to execute, pre‐recorded by the therapist. This allowed participants to easily perceive motion errors and adjust them during the task
Control intervention: 'conventional' rehabilitation focused on the upper limb
Sessions were 60 minutes, 5 times a week for 5 to 7 weeks (approximately 25 to 35 hours total)
Outcomes Outcomes recorded at baseline and post‐intervention
Upper limb function and activity outcomes (arm): Fugl Meyer UE Scale
Activity limitation outcomes: Functional Independence Measure
Adverse events reported
Notes
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Low risk Personal correspondence with the author reports the use of a simple computer‐generated sequence
Allocation concealment (selection bias) Low risk Sealed, opaque envelopes
Blinding of outcome assessment (detection bias) All outcomes Low risk Blind
Incomplete outcome data (attrition bias) All outcomes High risk There were 3 drop outs from the control group and the analysis was per‐protocol
Selective reporting (reporting bias) Low risk No other outcomes were collected