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Effects of care partner type on outcomes from a multicomponent behavioral intervention for mild cognitive impairment
Zhigang Xie1, Stephanie Aghamoosa2, Gelan Ying3
1Department of Health Services Research Management and Policy College of Public Health and Health Professions University of Florida Gainesville Florida USA.
Introduction:
Multicomponent non-pharmacological interventions, such as the HABIT Healthy Action to Benefit Independence & Thinking® program, have shown promise for improving emotional well-being, functioning, and self-efficacy in both people with mild cognitive impairment (pwMCI) and their care partners. However, limited research has examined whether outcomes differ based on type of care partner who co-enrolls with the pwMCI.
Methods:
We analyzed data from 875 pwMCI-care partner dyads who completed the HABIT program. Multivariate linear mixed-effects regression models evaluated changes from baseline in outcomes by care partner type (spouse vs. non-spouse) at post-intervention, 6-months, and 12- months.
Results:
At post-intervention, pwMCI with spousal care partners demonstrated significant improvements across all outcomes from baseline, whereas those with non-spousal partners improved in five out of seven outcomes. Across subsequent follow-ups, pwMCI with spousal care partners showed sustained mean reductions in anxiety (post-intervention: -2.0; 12-month: -0.9) and increased compliance (post-intervention: 5.7; 12-month: 0.9). Everyday functioning in memory (post-intervention: -0.9; 12-months: 1.8) and executive functioning (post-intervention: -0.7; 12-months: 4.8) improved at post-intervention but declined thereafter. Spousal care partners reported reduced anxiety (-1.2) and depression (-1.3) at post-intervention, but by 12-months they experienced increased burden, anxiety, and depression relative to baseline. Non-spousal pwMCI-care partner dyads did not show significant change at 6 or 12-months.
Discussion:
The HABIT intervention may have more favorable outcomes for pwMCI and care partners in spousal compared to non-spousal dyads. These findings highlight the potential impact of care partner characteristics on both immediate and long-term response to behavioral interventions for MCI.
Highlights:
At post-intervention, people with mild cognitive impairment (pwMCI) with spousal care partners showed significant improvements across all outcomes, while those with non-spousal partners improved in five of seven outcomes.Gains attenuated over time for both spousal and non-spousal dyadsSpousal care partners reported reduced anxiety and depression at post-intervention, but by 12 months they experienced increased burden, anxiety, and depression relative to baseline.Non-spousal pwMCI-care partner dyads did not show significant change at 6 or 12 months.
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