Twenty-three persons were enrolled in a pilot randomized, controlled trial that compared CIM with traditional
therapies. A blinded observer rated the primary end point, the Action Research Arm Test (ARA). Inclusion criteria were
the following: ischemic stroke within 14 days, persistent hemiparesis, evidence of preserved cognitive function, and
presence of a protective motor response. Differences between the groups were compared by using Student’s t tests,
ANCOVA, and Mann-Whitney U tests.
Twenty-three persons were enrolled in a pilot randomized, controlled trial that compared CIM with traditionaltherapies. A blinded observer rated the primary end point, the Action Research Arm Test (ARA). Inclusion criteria werethe following: ischemic stroke within 14 days, persistent hemiparesis, evidence of preserved cognitive function, andpresence of a protective motor response. Differences between the groups were compared by using Student’s t tests,ANCOVA, and Mann-Whitney U tests.
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