How Caregivers Perceive Mild Cognitive Impairment

In term of religious mastery, how did a caregiver feel before and after his or her patient (spouse/ partner/ parent/ relative/ friend) was diagnosed with MCI?

In term of physical wellbeing, what has changed in the caregivers’ perspective since his or her patient was diagnosed with MCI?

In term of emotional wellbeing, what was the caregiver’s mood before and how did it changed after his or her patient was diagnosed with MCI?

In term of financial hardship, how did the caregiver’s activities change from before to after his or her patient was diagnosed with MCI?

Did culture or ethnicity play a role in the caregiver’s coping strategy toward his or her patient’s MCI diagnosis?

How does socioeconomic status impact the caregiver’s coping strategy toward his or her patient’s MCI diagnosis?

What action has the caregiver taken toward his or her patient’s MCI diagnosis?

What factors improve the caregiver’s life when he or she is taking care of his or her patient?

What factors worsen the caregiver’s life when he or she is taking care of his or her patient?

How well does a caregiver with MCI patients understand about his or her disease?

What interventions will a caregiver likely to take when his or her patient is first diagnosed with MCI?

Last Updated on