Interactions of oppositely charged macroions in aqueous solution give rise to intriguing aggregation phenomena, resulting in finite-size, longlived clusters, characterized by a quite narrow size distribution. Particularly, the adsorption of highly charged linear polyelectrolytes on oppositely charged colloidal particles is strongly correlated and some short-range order arises from competing electrostatic interactions between like-charged polymer chains (repulsion) and between polymer chains and particle surface (attraction). The charge inversion observed for the polyelectrolytedecorated primary particles has been recently explained in terms of correlated adsorption. In these systems, long-lived clusters of polyelectrolytedecorated particles form in an interval of concentrations around the inversion point. However, the mechanisms that drive the aggregation and stabilize, at the different polymer/particle ratios, a well defined size of the aggregates are not completely understood. Nor is clear the role that the correlated adsorption plays in the aggregation, although the importance of 'patchy interactions' has been stressed as the possible source of attractive interactions between colloidal particles. Different models have been introduced to explain the formation of the observed finite-size cluster phase. However a central question still remains unanswered, i.e., whether the clusters are true equilibrium or metastable aggregates. To elucidate this point, in this work, we have investigated the effect of the temperature on the formation of the clusters. We employed liposomes built up by DOTAP lipid interacting with a simple anionic polyion, sodium polyacrylate, over an extended concentration range below and over the isoelectric condition. Our results show that the aggregation process can be described by a thermally-activated mechanism.