The dynamic mechanical transitions present in the 2-hydroxyethyl methacrylate (HEMA) and 2,3-dihydroxypropyl methacrylate (DHPMA) homopolymers and two random copolymers, with one-to-one and three-to-one HEMA-to-DHPMA molar ratios, were examined by analyzing the dry xerogels and hydrogels at various states of hydration. The temperatures of the primary a transition and the secondary beta and gamma transitions were determined in the tension mode; the storage modulus and loss modulus as a function of temperature and frequency were recorded. The results were compared to the results obtained from dielectric analysis at low hydration using tan delta. The frequency dependence of the dispersions was calculated for the dry and hydrated states, using mechanical and dielectric data. The information obtained was used to elucidate the interaction between the polymer and the sorbed water. Analysis of the low temperature secondary gamma transition and secondary transitions resulting from polymer-water interactions was emphasized. During the initial hydration, the temperature maxima of the dielectric and mechanical secondary gamma transitions, and the transitions that appear in the presence of absorbed water increased as the DHPMA content increased. The apparent activation energy associated with the secondary transitions increased as well. All of this is, the result of stronger intermolecular interactions due to the increased density of hydrophilic moieties in DHPMA.