1973
DOI: 10.1093/ptj/53.12.1276
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Designs for Clinical Research

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Cited by 11 publications
(4 citation statements)
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“…Sequential medical trials (SMT) were chosen to be the method of experimental design and statistical analysis. 14,15 This sequential design was considered ideal because 1) sub jects could be admitted to the study as they became available, 2) comparisons could be made within the same subject, 3) no statistical computations were necessary, and 4) the experiment could be terminated as soon as statistical significance was achieved (ie, a predetermined number of subjects was not required).…”
Section: Discussionmentioning
confidence: 99%
“…Sequential medical trials (SMT) were chosen to be the method of experimental design and statistical analysis. 14,15 This sequential design was considered ideal because 1) sub jects could be admitted to the study as they became available, 2) comparisons could be made within the same subject, 3) no statistical computations were necessary, and 4) the experiment could be terminated as soon as statistical significance was achieved (ie, a predetermined number of subjects was not required).…”
Section: Discussionmentioning
confidence: 99%
“…When there are large differences in patient characteristics and individual recovery patterns within both the experimental and control groups, it becomes difficult to demonstrate differences between groups, in particular, when these effects of treatment are small compared to the extent and heterogeneous nature of developing spontaneous recovery. For this reason, a number of researchers advocate the inclusion of a large number of patients in stroke rehabilitation trials, whereas others prefer controlled single subject experimental designs or interrupted time series experiments [40,41,42]. A major advantage to this latter design is its control for subject homogeneity.…”
Section: Methodological Quality Of Stroke Rehabilitation Researchmentioning
confidence: 99%
“…Because of this phenomenon, until the early diagnostic process achieves a level of sophistication such that professionals may distinguish reliably between those infants likely and not likely to exhibit spontaneous recovery, research into the effectiveness of therapeutic intervention with this population, using control group methodology, will continue to generate spurious findings. In response to this, continued research in this area will use such alternatives as non parametric research designs (I) and increasingly sophisticated single-subjecl methodologies (51,52).…”
Section: Summary and Recommendationsmentioning
confidence: 99%