The electrical properties of the entropy stabilized oxides: Zr6Nb2O17, Zr6Ta2O17, Hf6Nb2O17, and Hf6Ta2O17 were characterized. The results and the electrical properties of the products (i.e. ZrO2, HfO2, Nb2O5, and Ta2O5) led us to hypothesize the A6B2O17 family is a series of mixed ionic-electronic conductors. Conductivity measurements in varying oxygen partial pressure were performed on A6Nb2O17 and A6Ta2O17. The results indicate that electrons are involved in conduction in A6Nb2O17 while holes play a role in conduction of A6Ta2O17. Between 900-950°C, the charge transport in the A6B2O17 system increases in Ar atmosphere. A combination of DTA/DSC and in-situ high-temperature X-ray diffraction was performed to identify a potential mechanism for this increase. In-situ high-temperature X-ray diffraction in Ar does not show any phase transformation. Based on this, it is hypothesized that a change in the oxygen sub-lattice is the cause for the shift in high temperature conduction above 900-950°C. This could be (i) Nb(Ta)4+- oxygen vacancy associate formation/dissociation, (ii) formation of oxygen/oxygen vacancy complexes (iii) ordering/disordering of oxygen vacancies, and/or (iv) oxygen-based superstructure commensurate or incommensurate transitions. In-situ high-temperature neutron diffraction up to 1050°C is required to help elucidate the origins of this large increase in conductivity.