Objectives. To investigate electrically conductive polymer composite materials (EPCMs) based on crystallizable polyolefins and electrically conductive carbon black for the production of self-regulating heaters; to study the mechanism of the occurrence of positive and negative temperature coefficients (PTC and NTC) upon heating such composites.Methods. A comprehensive study of the structure and properties of crystallizable EPCMs with electrically conductive technical carbon was carried out. In order to measure the electrical characteristics of the composites, they were compacted into plates to model polymer heaters. Contact electrodes made of an ungreased brass mesh were embedded in their ends. The temperature dependencies of the electrical characteristics of the samples were investigated in a modified thermal chamber of an FWV 633.10 Vicat softening temperature meter. The change in the degree of crystallinity was analyzed by means of differential scanning calorimetry with a NETZSCH DSC 204 F1 Phoenix calorimeter. The dilatometric and rheological characteristics of the samples were studied using an IIRT-AM melt flow index tester.Results. It was determined that the self-regulation ability (an abnormally high positive thermal coefficient of electrical resistance) of selfregulating heaters made of composites of crystallizable polyolefins with electrically conductive technical carbon cannot be explained by the thermal expansion of EPCMs alone. It was shown that in crystallizable polyolefin-based EPCMs, the inversion of the thermal coefficients of electrical resistance (transition from PTC to NTC) is associated with a change in the aggregate state of EPCMs and the beginning of its transition to a viscous-flow state. A mechanism involving a sharp increase in the electrical resistance of self-regulating crystallizable polyolefin-based composite with electrically conductive technical carbon was proposed and substantiated. This mechanism takes into account the additional shear deformation effect produced on the crystalline phase of the EPCM by numerous expanding melt microvolumes formed at the early stages of the melting process with a minimum change in the degree of crystallinity.