scholarly journals Care Recipient Diagnosis Moderates the Relationship Between Caregiver Worry and Vigilance

2021 ◽  
Vol 5 (Supplement_1) ◽  
pp. 971-971
Author(s):  
Katherine Craig ◽  
Shirit Kamil-Rosenberg ◽  
J Kaci Fairchild

Abstract Family members of persons diagnosed with dementia or a traumatic brain injury (TBI) are often relied upon to provide daily support to their care recipients. However, research on the differing experiences of caregivers based on care recipient diagnosis is limited. The aim of this study was to examine the impact of worry and feelings of vigilance among caregivers of people with cognitive impairment due to either TBI or dementia. This sample included 61 caregivers (88.5% female, mean age 57.3±15.5) of persons with either a TBI (n = 32) or dementia (n = 29). Worry was assessed with the Penn State Worry Questionnaire and Vigilance was assessed with the Caregiver Vigilance Scale. Linear regressions revealed that after controlling for age, care recipient diagnosis moderated the relationship between worry and caregiver vigilance. Specifically, worry was significantly associated with caregiver vigilance in those caring for someone with dementia; however, a similar relationship was not seen in those caring for someone with a TBI. This suggests caregivers of people with TBIs have a different experience of worry and vigilance than caregivers of people with dementia. These findings demonstrate the need for more research on the unique needs of caregivers of people with TBIs. Additionally, this research suggests interventions targeting worry may be particularly effective in supporting caregivers of people with TBIs.

Author(s):  
Hacer BELEN

Epidemics and pandemics are difficult periods for the affected community, specifically in the proliferation of mental health issues. In such adverse times, factors of psychological vulnerability such as propensity to worry and low emotional stability might have a detrimental effect on the mental health of the individuals. To investigate the impact of such factors on mental health, this study examined the impacts of propensity to worry and fear of COVID-19 on anxiety depending on the individuals’ levels of emotional stability. As a means of such investigation, this study was conducted based on quantitative data, and the research sample was selected using a convenient sampling method. Participants included 304 university students (71.6% were women and 28.4% were men; MAge = 22.37 ± 3.04) and responded to the Penn State Worry Questionnaire, Fear of COVID-19 Scale, Symptom Checklist-90 Revised, and 10-Item Personality Inventory. The moderated mediation analysis using PROCESS macro (Model 14) was performed to examine the study hypotheses. Results revealed that propensity to worry was associated with anxiety symptoms. Fear of COVID-19 mediated this link and emotional stability moderated the relationship between propensity to worry and anxiety. The findings showed that trait worry, trait emotional stability, and fear of COVID-19 are determinants of anxiety symptoms, suggesting that such factors are important in understanding these issues.


2015 ◽  
Vol 43 (10) ◽  
pp. 1607-1616 ◽  
Author(s):  
Zhihui Yang ◽  
Ruiming Wang ◽  
Hui Chen ◽  
Jiali Ding

We examined the relationship between personality and worry, and tested a mediation model in which intolerance of uncertainty (IU) mediated this relationship. Participants comprised 1,135 Chinese college undergraduates who completed the Chinese versions of the Penn State Worry Questionnaire, the Intolerance of Uncertainty Scale, and the Revised Eysenck Personality Questionnaire-Short Scale for Chinese. Results showed that neuroticism, extraversion, and IU were significantly correlated with worry. The paths between personality (neuroticism and extraversion) and worry, and the paths mediated by IU, were significant. Participants' IU mediated the relationship between personality factors of neuroticism and extraversion, and worry. The results indicated that IU can be considered as a partial mediator of the relationship between personality and worry.


2021 ◽  
Vol 11 (6) ◽  
pp. 455
Author(s):  
Guido Edoardo D’Aniello ◽  
Davide Maria Cammisuli ◽  
Alice Cattaneo ◽  
Gian Mauro Manzoni ◽  
Enrico Molinari ◽  
...  

Music therapy (MT) is considered one of the complementary strategies to pharmacological treatment for behavioral and psychological symptoms (BPSD) of dementia. However, studies adopting MT protocols tailored for institutionalized people with dementia are limited and their usefulness for supporting caregivers is under investigated to date. Our study aimed at evaluating the effects of an MT intervention according to Gerdner and colleagues’ protocol in a sample of 60 elderly people with moderate-to-severe dementia of the Auxologico Institute (Milan, Italy) and associated caregivers, randomly assigned to an Experimental Group (EG) (n = 30) undergoing 30 min of MT two times a week for 8 weeks and to a Control Group (n = 30) (CG) receiving standard care. Before and after the intervention, residents-associated caregivers were administered the Caregiver Burden Inventory (CBI) and the Neuropsychiatric Inventory (NPI). Depression and worry were also assessed in caregivers prior to the intervention, by the Beck Depression Inventory-II and the Penn State Worry Questionnaire, respectively. A mixed model ANCOVA revealed a Time*Group effect (p = 0.006) with regard to CBI decreasing after the intervention for the EG and Time*Group effects (p = 0.001) with regard to NPI_frequencyXseverity and NPI_distress, with a greater effect for the EG than the CG. Implications for MT protocols implementations are discussed.


Author(s):  
Janice M. Keefe ◽  
Pamela J. Fancey

ABSTRACTThis research broadens the understanding of the relationship between paid work and caregiving by including the contribution of the older “care recipient”. Using selected aspects of social exchange theory and a life course perspective, the importance of giving and receiving for caregivers and care recipients is explored through analyses of focus groups with employed women and interviews with their older mothers. The mothers and daughters focus on the time when they are most indebted to each other. The daughter's employment affects the type and value of contributions from care recipients. The mother's past assistance with housework and caring for children is greatly valued by the daughters. For care recipients, however, being reliant on a busy employee for their care has negative consequences. The mothers emphasize the current situation and under-estimate their past helping. Further research should consider the care recipient's perspective to obtain a broader understanding of the impact of the caregiver's employment in caregiving relationships.


2020 ◽  
Vol 8 ◽  
pp. 387-397
Author(s):  
Khin Theint Theint Soe

The impact of social support buffers most of the psychological problems such as loneliness and worry in the transition period for university freshmen. This loneliness and worry can lead to many freshmen suffering in less confidence and difficulties in interactions as a university student. The greater perceiving social support can alleviate loneliness and worry. The main aim of this study is to investigate the impact of social support on loneliness and worry among university freshmen. In this study, a quantitative approach was used. The sample was composed of 500 freshmen from four universities, Sagaing Technological University, Sagaing University of Education, Co-operative University (Sagaing) and Sagaing University. Social support perceived by university freshmen was measured by using Interpersonal Support Evaluation List (ISEL) including four subscales that are appraisal support, tangible support, self-esteem support and belonging support which consisted of 40 items. The Loneliness of freshmen was examined by using the Revised UCLA Loneliness Scale (RULS) consisted of 20 items. Freshmen’s worry was explored by using the Penn State Worry Questionnaire (PSWQ) which comprised of 16 items. According to descriptive statistics, all universities in the selected district gave the equal social supports to freshmen but freshmen felt that they perceived the appraisal support than other supports. The results of independent sample t-test showed that there were significant differences in social support, loneliness and worry by gender. Furthermore, the result of ANOVA showed that there were significant differences in loneliness and worry by universities. The result of correlation analyses described that there was significant interrelationship among social support, loneliness and worry. The results of this study highlighted that types of social support can impact on loneliness and worry of freshmen effectively. That is the main reason why social support should be provided as one of the effective ways to ease loneliness and worry for freshmen.


2006 ◽  
Vol 12 (2) ◽  
pp. 196-203 ◽  
Author(s):  
E W Thornton ◽  
S Tedman ◽  
S Rigby ◽  
H Bashforth ◽  
C Young

This study examined the nature of worry in adult patients with multiple sclerosis (MS) in the UK. A measure of worry in MS was developed and the relationship between worry and standard scale measures of anxiety and depression was examined. Thirty-nine patients with MS and 40 controls completed the new worry scale (WQMS) that was psychometrically evaluated, together with the Penn State Worry Questionnaire (PSWQ), the Hospital Anxiety and Depression Scale (HAD) and a previously developed scale to assess self-efficacy in MS (SESMS). The scores for both anxiety ( t=2.34; p<0.05) and depression ( t=5.52; p<0.01) were higher in MS patients than controls, as was the new scale for worry - the WQMS. A factor analysis (explaining 65.73% of the variance) suggests that the worries of patients may be dichotomized into those concerned with the physical effects of the disease and those relating to the impact on social interaction, family relationships and daily activity in the home and/or work. Worry in patients with MS was associated with a decreased sense of being able to produce positive activities or effect positive outcomes (low self-efficacy). The questionnaire provides a framework for investigation in clinic of specific concerns and level of worry they engender.


2009 ◽  
Vol 65 (2) ◽  
pp. 69-75 ◽  
Author(s):  
Colin van der Heiden ◽  
Peter Muris ◽  
Arjan E. R. Bos ◽  
Henk van der Molen ◽  
Martijn Oostra

Author(s):  
João Tiago Oliveira ◽  
Divo Faustino ◽  
Fátima Freitas ◽  
Miguel M. Gonçalves ◽  
Eugénia Ribeiro ◽  
...  

2020 ◽  
Vol 4 (Supplement_1) ◽  
pp. 152-152
Author(s):  
Afeez Hazzan

Abstract Family caregivers of older people living with dementia are relatives, friends, or neighbors who provide assistance related to this condition, but who are unpaid for the services they provide. Although caregiving could be personally rewarding, many caregivers report a high level of strain. Compared to caregivers of older adults who do not have dementia, family caregivers of older people living with dementia report lower quality-of-life (QoL). In a published systematic review examining the relationship between family caregiver QoL and the quality of care provided, only one study was found to be somewhat relevant. The study suggested that the primary reason for an absence of research into the link between family caregiver QoL and quality of care was the absence of a questionnaire for measuring quality of care in dementia. Therefore, any attempt to investigate the impact of caregiver QoL on the care provided to older people with dementia must first address the lack of an instrument to measure quality of care. To address this issue, we interviewed approximately 20 family caregivers in order to elicit feedback on measurements and interpretation of the quality of care provided by family caregivers of older people living with dementia. Content analysis of the interview transcripts revealed that the quality of relationships with family, caregiver availability to provide or supervise care, and availability of paid or volunteer help are important for the quality of care provided. These results have important implications, particularly for the development of an instrument to measure quality of care in dementia.


2020 ◽  
Vol 12 (20) ◽  
pp. 8493
Author(s):  
Paloma Escamilla-Fajardo ◽  
Juan M. Núñez-Pomar ◽  
Ferran Calabuig-Moreno ◽  
Ana M. Gómez-Tafalla

Sports entrepreneurship has been considered an important part of sports organisations when overcoming crisis situations. The aim of this study is to determine the impact of the crisis derived from COVID-19 on sports entrepreneurship and whether there are differences in the prediction of entrepreneurship on service quality in non-profit sports clubs. To this end, 145 sports clubs were analysed before and after the outbreak of the virus in society. Paired sample-t tests were carried out to determine the differences in variables studied before (Time I) and after (Time II) the COVID-19 outbreak, and correlations and hierarchical linear regressions were used to analyse the relationship between the variables studied in the two different stages. The results obtained show that risk-taking and innovation are significantly higher after the appearance of COVID-19, while proactivity has not undergone significant changes. Finally, the relationship between sports entrepreneurship and service quality is positive and significant in both stages but stronger before the crisis.


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