Clinical assessment of rigidity in parkinsonian patients is largely qu
alitative. The reliability and validity of the assessments are sometim
es in doubt. Several ''engineering'' methods of quantifying rigidity h
ave been described, but none has been adopted into general clinical pr
actice. A possible reason is that these methods differ in crucial aspe
cts from the clinical exam. We therefore tackled the problem by monito
ring the clinical exam itself, using small sensors to measure the forc
es and displacements applied. Limb impedance (Z) was computed using pa
rameter identification methods and compared to raters' verbalized rati
ngs of rigidity based on a 5-point scale: the Unified Parkinsons Disea
se Rating System. The qualitative and quantitative estimates of impeda
nce covaried over a fourfold range, depending on the fortes imposed an
d the subject's motor set. Raters differed by up to 1 full point in th
eir mean qualitative ratings and sometimes disagreed on whether levodo
pa reduced rigidity, This was not due to any significant differences i
n the overall range of rigidity they evoked, but rather to the way the
y scored this range [the ratio of mean rating to mean impedance (R/Z)
varied between raters and subjects]. On the other hand. the R/Z ratio
was reproducible over separate sets of ratings and may therefore serve
to convert measured impedance into a standardized rating. Our results
indicate that the current clinical exam may be too abbreviated to det
ect the sometimes quite small reductions in rigidity after levodopa. W
e conclude that a device that conveniently quantifies the clinical ass
essment of rigidity is now available and will lead to more standardize
d protocols for rating rigidity in the near future.