Family Caregiving for Individuals with Parkinson’s Disease and Lewy Body Dementia
Author Information
Author(s): Whitney Robin, Bell Janice, Link Benjamin, Bhurtel Shikha, Ogugu Everlyne, Tonkikh Orly, Kelly Kathleen, Young Heather
Primary Institution: San Jose State, UC Davis, Family Caregiving Alliance
Hypothesis
Care recipient condition predicts caregiving outcomes among caregivers of individuals with PD/LBD compared to those with ADRD and other chronic conditions.
Conclusion
Caregivers of individuals with PD/LBD experience higher caregiving strain and worsening health compared to those caring for individuals with other conditions.
Supporting Evidence
- PD/LBD caregivers were more likely to care for a spouse and spend over 40 hours a week on caregiving.
- They assisted with more personal care compared to caregivers of other conditions.
- Caregiving for PD/LBD was associated with increased caregiving strain and worsening health.
Takeaway
Taking care of someone with Parkinson’s or Lewy Body Dementia is really hard, and it can make caregivers feel more stressed and unhealthy.
Methodology
Data was extracted from CareNavTM, a statewide electronic platform, and multivariable logistic regression models were used to analyze caregiving outcomes.
Limitations
The study primarily focuses on caregivers in California and may not represent caregivers in other regions.
Participant Demographics
Majority of caregivers were older, female, white, college-educated, and retired.
Statistical Information
P-Value
0.01
Confidence Interval
95% CI [1.0-1.4]
Statistical Significance
p<0.01
Digital Object Identifier (DOI)
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