Nys 2008.
| Methods | RCT "single‐blind randomised controlled design" Setting: Netherlands | |
| Participants | 16 participants with neglect from 3 stroke units Experimental: n = 10 , control: n = 6 Adequacy of matching at baseline? Yes Number lost to follow‐up: not clear ‐ only those who completed were included in the report. Also excluded 1 patient with deterioration of neurological condition during treatment phase , which probably should have been a loss to follow‐up rather than exclusion Mean age (mean (SD)): experimental = 63.6 (13.8), control = 61.5 (11.0) years Sex (male/female): experimental = 7/3, control = 3/3 Time post‐onset: experimental 1 = 8.8 (5.3), control = 11.2 (6.4) days Side of damage: right Method of diagnosing stroke: not stated, was based on the referral by a stroke physician on their admitting SU Method of diagnosing neglect: 2 or more subtests (out of 4): BIT subtests below cut‐off. The four tests were Star Cancellation (cut‐off ≤ 51), line bisection (cut‐off ≤ 7), figure copying (cut‐off ≤ 2) and representational drawing (cut‐off ≤ 2) Inclusion criteria: inpatient in SU with neglect, within 4 weeks post‐stroke. All participants had to demonstrate an after‐effect of at least 3 visual degrees to the left of the landing position after the first prism adaptation; this would only apply to the active treatment group, but none were excluded for this reason Exclusion criteria: ocular problems, a disturbed consciousness or a too limited attention span (participants excluded during screening) Visual sensory deficit: 2 in the experimental group had hemianopia, diagnosed by confrontation comparing cueing and non‐cueing conditions by a stroke neurologist |
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| Interventions | Prism adaptation: "an extended version of that used by Rosetti et al 1998". While wearing goggles with prisms inducing a rightward optical shift of 10°, participants made 100 fast pointing movements to 2 visual targets presented 10° to the left and right of the body midline. Sessions of 30 minutes were conducted 4 days in a row versus placebo ‐ as above but wearing goggles with no optical shift. Sessions of 30 minutes were conducted 4 days in a row
For analysis of bottom‐up and top‐down rehabilitation approaches this review coded the experimental condition as bottom‐up Profession of intervention provider not stated |
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| Outcomes |
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| Notes | Postulated mechanism of action: not clear but stated there was a "neural basis for the therapeutic effect" and treated early because the brain is most sensitive to rehabilitative treatment early after stroke | |
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Allocation concealment (selection bias) | Unclear risk | Insufficient details "according to a randomisation procedure in SPSS" |
| Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Only 1 measure, scene copying, appears to have been scored retrospectively by an independent rater. Not stated if outcome assessor was blinded |
| Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Unclear ‐ only those who completed were included in the report |
| Free of systematic differences in baseline characteristics of groups compared? | Unclear risk | Removed 1 person who failed to complete treatment but no indication of which group this was from |
| Did authors adjust for baseline differences in their analyses? | Low risk | Not necessary |