International Journal of Alzheimer’s Disease / 2021 / Article / Tab 4 / Research Article
Improving the Quality of Life of Family Caregivers of People with Alzheimer’s Disease through Virtual Communities of Practice: A Quasiexperimental Study Table 4 Statistical differences between qualitative caregivers’ variables and QoL.
Variable N Mean diff. overall QoL_change SD overall QoL_change Overall QoL value Physical QoL value Psycho. QoL value Social QoL value Environ. QoL value Age 37 0.025 0.566 0.008 0.270 0270 ≤64 28 1.08 15.84 >65 9 8.33 6.48 Gender 37 0.479 0.148 0.094 0.0957 0.871 Male 8 7.53 13.60 Female 29 1.54 14.57 Level education 37 0.760 0.119 0.153 0.907 0.999 Primary 7 6.14 8.83 Secondary 17 4.39 14.54 University 13 -0.94 16.62 Marital status 37 0.092 0.440 0.633 0.285 0.225 Married 27 4.06 11.63 Single 4 -14.02 26.11 Divorced 6 8.70 10.08 Offspring number 37 0.415 0.358 0.255 0.684 0.832 None 8 -4.18 21.79 One 7 8.29 13.50 Two 16 4.66 11.57 Three 6 0.29 7.67 Relation/person with Alzheimer’s 37 0.045 0.132 0.042 0.918 0.292 Offspring 29 2.98 15.69 Spouse 5 7.80 4.78 Other 3 -6.75 6.24