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. Author manuscript; available in PMC: 2021 Dec 1.
Published in final edited form as: J Cross Cult Gerontol. 2020 Dec;35(4):479–492. doi: 10.1007/s10823-020-09410-y

Table 4.

Means (M) and standard deviations (SD) of outcome data (N =11)

Baseline Post-Assessment 3-Month Follow-Up
M SD M SD M SD
Caregivers
 Burden 23.64 9.88 21.82 8.76 18.90 12.39
 Self-efficacy
  Symptom management 5.48 2.24 6.53 1.69 6.22 1.14
  Support services 2.82* 1.65 6.00* 1.75 6.18* 1.52
 Knowledge of Alzheimer’s disease 20.90* 2.42 22.55* 2.07 22.20 2.57
 Perceived stress 15.00 5.98 12.23 6.86 13.10 5.88
 Intention to use services 4.09 .45 3.77 .56 3.48 .47
Care recipients
 Quality of life 1.95 .45 2.05 .48 2.11 .29
 MOCA 8.0 4.90
 IQCODE 4.60 .49
*

p < .05. One caregiver missed follow-up data. Only 7 care recipients had MoCA scores.