We use the x-ray diffraction, magnetic susceptibility, isothermal magnetization, and photoelectron spectroscopy to study the structural, magnetic and electronic properties of La (1−x) AxCoO3 (A = Sr, Ca; x = 0 -0.2) nanoparticles. The Rietveld refinements of room temperature powder x-ray diffraction data confirm the single phase and the rhombohedral crystal structure with R3C space group. We find drastic changes in the magnetic properties and spin-states with Sr/Ca substitution (hole doping). For x = 0 sample, the magnetic measurements show a ferromagnetic transition at TC≈85 K, which shifted significantly to higher temperatures with hole doping; simultaneously a significant increase in the spontaneous magnetic moment has been observed. Whereas, the coercive field HC values are 7, 4.4 and 13.2 kOe for x = 0, 0.2 (Sr), and 0.2(Ca) samples. Furthermore, the FC magnetization shows a ferromagnetic Brillouin function like behavior at low temperatures for Ca samples. We demonstrate that the Sr/Ca substitution increases the population of IS (Co 3+ ) and LS (Co 4+ ) states and tune the ferromagnetism in nanoparticles via double-exchange interactions between Co 3+ -Co 4+ . Our results suggest an important role of hole carriers and nano-size effect in controlling the spin-state and magnetism in La (1−x) AxCoO3 nanoparticles.