In the present work, we investigate the dependence of relaxational pro
cesses in strongly confined polymer liquids as a function of the molec
ular mass and of the confining film thickness, both theoretically and
experimentally. A qualitative agreement is observed between the theore
tical predictions and experimental findings. On the basis of the propo
sed theory and experimental data, we estimate the relaxation time of t
he polymer segments in the first surface layer and far away from the s
urfaces as well as the maximum stress relaxation time.