key: cord-0805657-8j8l2bsk
authors: Altieri, Manuela; Santangelo, Gabriella
title: The psychological impact of COVID-19 pandemic and lockdown on caregivers of people with dementia
date: 2020-10-22
journal: Am J Geriatr Psychiatry
DOI: 10.1016/j.jagp.2020.10.009
sha: f05ec2d8d542e2e41c76a38dea8ff94eec4dcf12
doc_id: 805657
cord_uid: 8j8l2bsk

BACKGROUND: Caregivers of people with dementia (pwD) are at risk of depression, anxiety and burden. COVID-19 pandemic and government-imposed lockdown as a preventive measure might increase psychological symptoms in caregivers. We performed a study to measure the change of psychological symptoms during quarantine/self-isolation for COVID-19 in a sample of Italian caregivers of pwD, and to investigate if the resilience is associated with psychological changes in the sample. METHODS: Eighty-four caregivers of pwD completed an online survey including questionnaires assessing depressive symptomatology and anxiety before and during the lockdown, caregiver burden and levels of resilience. RESULTS: The MANOVA revealed an effect of time (before and during the lockdown) in the whole group on depression scores; a significant interaction between time and resilience was found on anxiety scores, revealing that caregivers with high resilience showed a more significant increase of anxiety levels during lockdown than caregivers with low resilience. Moreover, the regression analysis revealed that caregiver burden was associated negatively with resilience scores, and positively with higher functional dependence. CONCLUSIONS: COVID-19 pandemic and the lockdown produced psychological consequences in caregivers of pwD, with an increase of levels of depression. Moreover, high resilience had a negative effect on anxiety levels and no effect on depressive symptomatology during the lockdown; moreover, it was associated with lower levels of caregiver burden. All caregivers, even those with high resilience levels, should be addressed to psychological interventions to reduce levels of depression, anxiety and caregiver burden.

In late 2019, the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was detected as the causative agent of COVID-19, a respiratory disease that was first noticed in China and quickly spread out in Europe and in at least 216 countries, areas or territories throughout the world 1 .Several studies revealed that premorbid conditions and/or older age were risk factors for COVID-19 mortality, and the pandemic was called the "geriatric emergency of 2020" 2 .

Among older people, people with dementia (pwD) may be at higher risk of fatal outcomes due to COVID-19 outbreak, because of the vulnerability due to their disease and to the indirect effect of pandemic on social and medical support 3 . Given the extreme uncertainty of the pandemic, informal caregivers of pwD (relatives or friends who are not paid for their assistance) may face new challenges during this period: in fact, caregiving activities may be more struggling because of lockdowns imposed by governments, social distancing, difficulties in fulfill the basic needs of pwD and accessing to the National Healthcare System or private physicians during the COVID-19 pandemic. Providing care for older frail adults, and in particular for pwD, is already a stressful experience that may have a negative impact on psychological well-being 4 ; in fact, 34% of caregivers report depressive symptomatology and the 43.6% report high levels of anxiety 5 .

However, in some caregivers, psychological distress may be buffered by high levels of resilience, a multidimensional construct that reflects the ability to resist or adapt to physical and psychological challenges of caregiving 6, 7 .

In a pandemic characterized by extreme uncertainty, it is possible that the lockdown may have exacerbated psychological reactions such as anxiety and depression in caregivers of pwD.

Taking into account that resilience is the ability to mentally or emotionally cope with stressors 5 , caregivers with a low level of resilience should be more prone to an increase of psychological symptoms. Therefore, in the present study, we evaluated possible changes in depression, anxiety in caregivers of pwD during the Italian lockdown due to COVID-19 pandemic; moreover, we explored if during lockdown the levels of depression and anxiety increased more in caregivers of pwD with a low level of resilience than in ones with a high level of resilience.

An online survey was shared through a link on online groups dedicated to dementia patients and/or caregivers, online newspapers, associations of caregivers of pwD (i.e., Alzheimer's Disease, Vascular Dementia, Frontotemporal Dementia). The study was approved by the local ethical committee. The online survey started with an informed consent form. Data were collected between April 21st and May 3rd during the Italian lockdown due to Covid-19 pandemic.

The online survey included 1. a socio-demographic questionnaire aimed at collecting demographic information about respondents and clinical information about their relatives with dementia (i.e., type of diagnosis, level of functional dependence, disease duration), the relationship with the pwD, their caregiving habits and their lifestyle changes during the lockdown; 2. The Italian version of Hospital Anxiety and Depression Scale (HADS) 8 to evaluate levels of anxiety and depressive symptomatology. The HADS scale provides two indexes to evaluate anxiety (HADS-A) and depression (HADS-D). Higher scores are indicative of higher anxiety and depression. For the purposes of this study, participants were asked to complete twice the questionnaire in order to describe how they felt immediately before the lockdown, and during the lockdown; 3. The Italian version of the Resilience Scale for Adults (RSA) 9 , a selfadministered questionnaire that evaluates levels of resilience. The RSA provides a total score and six subscores (perception of self, planned future, social competence, structured style, family cohesion, social resources) and higher scores indicate higher levels of resilience. 4. the Italian version of Caregiver Burden Inventory (CBI) 10 , a multidimensional scale that evaluates multiple aspects of caregiver burden (time-dependence, developmental, physical, social, and emotional burden). Participants were asked to complete the questionnaire by taking into account how they felt during the lockdown. Higher scores are indicative of higher burden.

Statistical analyses were performed by using SPSS Statistics version 25.0. Means and standard deviations, or percentage were used to describe continuous or categorical variables, when appropriate. A multivariate analysis of variance (MANOVA) for repeated measures was used to evaluate a) possible changes of depression and anxiety levels over time (before and during the lockdown) on the whole sample; b) possible differences on levels of depression and anxiety before and during the lockdown between caregivers with high and low resilience levels.

Dependent variables were HADS-D and HADS-A scores before the lockdown (time point 1) and during the lockdown (time point 2); the independent variable was the RSA level (high/low resilience). Since no cut-off was provided for the RSA scale, RSA dichotomous level was computed by calculating the median score of RSA on the whole sample; caregivers who scored under or above the median score were sorted in the low resilience or high resilience group, respectively. Partial eta square (partial η 2 ) was calculated and used as a measure of effect size; the interpretation of the magnitudes of effect sizes was based on the following cut-offs 11 : .01, .06, .14 for small, medium and large effect sizes, respectively. Moreover, univariate analysis of variance (ANOVA) was performed to evaluate the effect of each independent variable on the abovementioned dependent variables.

To evaluate the association between caregiver burden during the lockdown and sociodemographic and psychological variables, multiple regression analysis (stepwise method) was performed. The standardized coefficients (beta) were calculated. CBI score was entered as dependent variable, while delta scores of HADS-D and HADS-A (during lockdown score minus pre-lockdown score), RSA scores, days in lockdown, years of education, employment status before the lockdown, change in working modality, type of diagnosis of dementia of pwD, level of functional dependence, disease duration of pwD, and time of care were entered as independent variables.

Moreover, an ANOVA was performed to verify possible differences in HADS-A, HADS-D, CBI and RSA scores between caregivers of patients with Alzheimer's Disease and non-Alzheimer's Dementia.

To reduce the possibility of type I error, each critical p value for multiple comparison was adjusted by using the Benjamini-Hochberg procedure 12 , with a false discovery rate of .05.

Eighty-four participants (71 women, 13 men) agreed to participate in the study and completed the online survey. Mean age of the sample was 48.7 years old, and mean years of education were 13.8. As regards the working status, the 54.8% of the sample was employed immediately before the lockdown; among the workers, after the lockdown, the 59.5% of the sample stopped working, the 17.9% switched to smart-working, the 2.4% reduced their working time, and the 20.2% worked in the same modality as before. All socio-demographic and clinical characteristics of the sample are depicted in Table 1 and 2.

Neither the caregivers nor the pwD of our sample were tested positive for COVID-19 nor they showed symptoms related to COVID-19. In order to prevent SARS-CoV-2 infection, 56% of the sample reported using disposable gloves, the 72.3% wore protective masks, the 73.8%

increased the frequency of housecleaning, and the 60.7% engaged in social distancing. When asked about how much the pwD was aware of the pandemic situation, the 79.8% of the caregivers reported that his/her relative with dementia was unaware of the situation. According to their caregivers, the SARS-CoV-2 outbreak and the lockdown had an impact on the lifestyle of 50% of pwD. Moreover, when asked about the dangerousness of getting COVID-19, the 75% of the caregiver sample felt that the COVID-19 pandemic was a threat for their own health, whereas the 82.1% of the sample reported that it was a health threat for pwD. Finally, a between-group analysis was performed on caregivers of people with Alzheimer's disease and non-Alzheimer's Dementia and no differences were found on levels of depression and anxiety (both before and during the lockdown), resilience and caregiver burden (see Table   3 ).

The present study aimed at investigating levels of depressive symptomatology, anxiety, resilience and caregiver burden in a sample of Italian dementia caregivers during the 2020 lockdown due to COVID-19 pandemic. Firstly, when we analyzed the whole group of caregivers, we found a significant influence of time, with a medium effect size, on the severity of depressive symptoms rather than anxiety due to lockdown. Our results suggested that psychological changes are associated with the introduction of the restrictions applied by the Government during the COVID-19 pandemic, such as social distancing and limitations in individual mobility and social activities. These restrictions may have had negative consequences on the possibility of being psychologically and emotively supported by others; low social support is associated with higher depression in caregivers, as found in several studies 13, 14 . First reports on immediate psychological responses in Italy during the lockdown revealed an increase of levels of depression and anxiety in general population 15 . Our study confirmed an increase of depressive symptomatology, but not anxiety, during the lockdown. However, the divergent results on anxiety might be due to the different study sample: we focused on caregivers of pwD, whereas Mazza and colleagues recruited general populations.

Moving on the comparisons between caregivers with high and low resilience levels, we found a large effect size of resilience on the severity of depression and anxiety in caregivers; in fact, caregivers with high resilience reported lower levels of depression and anxiety before the lockdown when compared with caregivers with low resilience. Surprisingly, we found that caregivers with high resilience reported a significant increase of levels of anxiety during the lockdown, whereas in caregivers with low resilience no significant increase of anxiety levels was found, with a medium effect size of the time x resilience interaction. Although high resilience is considered a protective factor against depression and anxiety in caregivers 16 , these findings may suggest that resilience might not have a protective effect on caregivers' psychological status during non-ordinary global events, like a pandemic, and that these events may nullify the advantages of having high resilience (i.e., showing lower levels of anxious symptomatology). Our results highlight the need of developing specific programs for caregivers of pwD, even in those with high resilience, aimed at acquiring coping strategies and life skills.

Moreover, since loneliness and social isolation are common features of caregiving 17 , support groups and/or psychological interventions via the internet should be implemented to reduce depression and anxiety levels, especially during emergencies that affect the whole population, as in the case of COVID-19 pandemic.

Moving on results on caregiver burden, we found that lower levels of resilience and a higher functional dependence of pwD predicted higher levels of caregiver burden during the lockdown.

Our results are in line with a previous study 16 suggesting that resilience may be a protective factor against caregiver burden even in case of global emergencies, like the COVID-19 pandemic.

On the contrary, unlike previous studies that failed to find an association between caregiver burden and functional dependency of caretakers 16, 18, 19 , we found a significant and positive relationship. The divergence between results may be due to methodological differences in study design and/or scales to evaluate activities of daily living, or to the psychological reaction caused by the lockdown: in fact, caregivers of pwD with higher dependence on their activities of daily living may have had more difficulties in carrying on their care routine and be more psychologically and physically stressed due to the restrictions imposed by governments.

Lastly, our data offered no evidence that the diagnostic type of dementia of the patients influence levels of psychological distress and burden in caregivers, both before and during the lockdown. Previous comparative studies provided inconsistent results [20] [21] [22] , probably due to different study designs and to the use of different scales to evaluate burden, depression and anxiety, so further research is needed to further explore this topic. However, in our study we found that during the lockdown due to COVID-19 pandemic all caregivers of pwD reported the same psychological consequences, regardless of the type of diagnosis of dementia of their carers.

Our study is not exempt from limitations. Firstly, ours is not a longitudinal study since we assessed levels of anxiety and depression by asking participants, during the lockdown, how they felt both during and before the lockdown. This may have caused a possible recall bias. However, the recall bias is more likely to occur when the time interval between two or more events is high 23 ; in our study, we asked to report how participants felt just before the lockdown, in order to limit the presence of the recall bias. Moreover, since participants were not cognitively assessed by means of specific screening tools, nor they completed a personality assessment, they may have underestimated or overestimated their symptoms before and during the lockdown. Finally, participants participated on a voluntary basis, so the sample may be not representative of the population.

Taken together, our results show that the COVID-19 pandemic and the lockdown as restrictive measure against COVID-19 produced psychological changes in caregivers of pwD, with an increase of levels of depression rather than of anxiety. Furthermore we found that, even if high resilience in caregivers of pwD was associated with lower levels of caregiver burden, it had a negative effect on levels of anxiety during the lockdown, and that the magnitude of abovementioned effect sizes was medium to large, corroborating the clinical meaningfulness of our results. For these reasons all caregivers -not only those with low levels of resilience, and regardless of the clinical diagnosis of the caretaker -should be addressed to online psychological and educational programs to reduce their depressive symptomatology, anxiety and burden levels.

No disclosures to report.

Funding statement: the authors received no specific funding for this work. The values are expressed in mean ± standard deviation. HADS-A = Anxiety subscale of Hospital Anxiety and Depression Scale; HADS-D = Depression subscale of Hospital Anxiety and Depression Scale; CBI = Caregiver Burden Inventory; RSA = Resilience Scale for Adults. Degrees of freedom (df) = 1,82 in all models. F = F-statistics ANOVA; p = probability value. HADS-A = Anxiety subscale of Hospital Anxiety and Depression Scale; HADS-D = Depression subscale of Hospital Anxiety and Depression Scale; CBI = Caregiver Burden Inventory; RSA = Resilience Scale for Adults. Pvalues < 0.05 are considered statistically significant.

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