Table 5.
Author (year) | Purpose | Recruitment setting | Resilience scale or measure | Mean resilience score (SD) | Key results |
---|---|---|---|---|---|
Quantitative, cross‐sectional or longitudinal studies (n = 35) | |||||
Castellano‐Tejedor and Lusilla‐Palacios (2017) 58 | To describe a sample of caregivers of persons SCI, their burden of care, resilience and life satisfaction and to assess the relationships between these variables and other sociodemographic factors | SCI acute unit from a tertiary university hospital following discharge | The Resilience Scale |
141.93 (23.4) |
Half of the sample showed moderate–high resilience; few had low‐resilience scores. Resilience was not related to caregivers' demographics or SCI severity. Burden was negatively correlated with resilience. Resilience was positively correlated with relationship satisfaction |
Senturk et al. (2018) 59 | To examine the relationship between caregiver burden and psychological resilience in caregivers of PWD | Outpatient neurology department of a university hospital | The Resilience Scale for Adults |
111.25 (23.9) |
Negative correlation between the caregiver burden index and resilience scores |
Garity (1997) 76 | To investigate the relationship between stress level, learning style, resilience factors and ways of coping in AD family caregivers | Support groups of an AD association | The Resilience Scale | 144.4c | Participants were moderate–high on resilience scores and used problem‐ and emotion‐focused coping. Resilience positively correlated with emotion‐ and problem‐focused coping |
Scholten et al. (2020) 60 | To identify intra‐ and interpersonal sociodemographic, injury‐related and psychological variables measured at admission of inpatient rehabilitation that predict psychological distress among dyads of individuals with SCI or ABI and their significant others 6 months after discharge |
Part of a larger study conducted in regional rehabilitation centres |
Connor–Davidson Resilience Scale Short‐form |
28.2 (6.1) |
Higher baseline psychological distress, lower scores on adaptive psychological characteristics (combination of self‐efficacy, proactive coping, purpose in life and resilience), and higher scores on maladaptive psychological characteristics (combination of passive coping, neuroticism, appraisals of threat and loss) were related to higher psychological distress, as well as crosswise between individuals with SCI or ABI and their significant others |
Brickell et al. (2020) 77 | To examine factors related to resilience in military caregivers across health‐related caregiver QOL, caregiver sociodemographic variables and SMV injury and health status | TBI clinics at a National Military Medical Centre; Marine Corps base camp; community outreach activities | TBI‐QOL Resilience Short form |
55.6 (9) |
There were no differences across caregiver resilience groups (‘low‐moderate’, ‘moderate’, ‘moderate‐high’) for most demographics, SMV injury and health status variables. Low resilience was related to strain on employment due to caregiving duties, financial burden, caring for children, less personal time, caring for both verbal and physical irritability, anger and aggression and lower SMV functionality. Lower resilience was associated with poorer health‐related QOL scores across all groups |
Simpson and Jones (2013) 91 | To investigate the relationship between resilience and positive affect, negative affect and burden in caregiving; the relationship between resilience and helpfulness of caregiving management strategies; and the similarities and differences in resilience among family TBI versus ABI caregivers | Review of medical records and staff caseloads | The Resilience Scale |
140.2 (18.7) |
Positive correlation between resilience and positive affect. Resilience demonstrated a negative correlation with negative affect and burden scores. No link was found between resilience and the relatives' severity of functional impairment. Participants with high‐resilience scores rated certain caregiving strategies as more helpful than those with low‐resilience scores |
Cousins et al. (2013) 61 | To explore the influence of family caregivers on the uptake of NIV in persons with MND | Specialist neurology and respiratory clinics | The Dispositional Resilience Scale |
NIV |
Caregivers supporting NIV treatment were more resilient. Caregiver resilience (commitment) was the strongest predictor of uptake of NIV treatment |
88.63 (13.2) | |||||
Decliners | |||||
73.50 (15) | |||||
Elnasseh et al. (2016) 62 | To examine whether healthier family dynamics are associated with a higher sense of coherence, resilience and optimism in dementia caregivers in Latin America | Regional Neuroscience Institute | The Resilience Scale for Adults |
204.29 (21.8) |
Family dynamics explained 32% of the variance in resilience. Income was associated with resilience. Greater family empathy and decreased family problems were associated with higher resilience |
Ertl et al. (2019) 63 | To examine whether resilience moderates the relation between perceived stress and health‐related QOL among PD caregivers in Mexico | Outpatient neuropsychological services at the National Neuroscience Institute | The Brief Resilience Scale |
21.28 (4.4) |
Resilience moderated the inverse relationship between perceived stress and mental health‐related QOL. Resilience did not moderate the relation between stress and physical health‐related QOL |
Fitzpatrick and Vacha‐Haase (2010) 78 | To examine the relationship between resilience and marital satisfaction in caregivers of spouses with dementia | Gerontology Research Unit at regional hospital and local caregiver support groups | The Shortened Resilience Scale |
5.5 (0.8) |
Resilience was not correlated with marital satisfaction. Marital satisfaction was influenced most by caregiver burden (negative influence) and caregiver age (positive influence) |
Kimura et al. (2019) 87 | To investigate the relationship between clinical symptoms of people with young‐onset Alzheimer disease (YOAD) and carer resilience | AD outpatient clinic at the University Institute of Psychiatry | The Resilience Scale |
141.4 (13.5) |
Carers showed moderate to high levels of resilience. No relationship was found between carer resilience and both carer and care‐recipient sociodemographic characteristics. No relationship was found between career resilience and clinical symptoms of persons with YOAD. Resilience was inversely associated with carers' depressive symptoms |
Ruisoto et al. (2020) 64 | To examine factors that predict burden in a sample of family caregivers of PWD | Referral lists of the associations of relatives of people with AD and other dementias, neurology outpatient clinics and the national reference centre of AD | The Connor‐Davidson Resilience Scale |
73.9 (13.7) |
Caregiver burden correlated negatively with resilience. Resilience explained 18.7% of variance in social support and social support accounted for 46.11% of variance in burden. Social support partially mediated the relationship between resilience and burden in caregivers |
Scott (2013) 46 | To examine the moderating effect of resilience between caregiver stressors and caregiver burden | Community agencies that provide education and support to AD caregivers in the region | The Resilience Scale | NR | Resilience was not identified as a moderator of the relationship between stressors and caregiver burden. An inverse relationship existed between resilience and caregiver burden |
Pessotti et al. (2018) 88 | To evaluate family caregivers' perception of QOL, burden, resilience and religiosity and relate them with cognitive aspects and occurrence of neuropsychiatric symptoms of elderly persons with dementia | Clinical Neurology Outpatient Clinic at the regional hospital | The Resilience Scale |
135.6 (22.5) |
Resilience was associated with better perceived QOL, severity of dementia, higher intrinsic religiosity and lower occurrence of depressive symptoms |
Wilks and Vonk (2018) 79 | To explore whether the coping method of private prayer served as a protective factor or mediator between caregiver burden and perceived resiliency among AD caregivers | Regional AD association caregiver support groups | The Connor–Davidson Resilience Scale |
73.4 (13.4) |
Burden positively affected the extent of prayer usage and negatively influenced resilience. Caregiver burden and private prayer influenced variation in resilience scores. Results support prayer as a mediator between burden and resilience |
Rosa et al. (2020) 90 | To investigate resilience in caregivers of people with mild and moderate AD and the related sociodemographic and clinical characteristics | Outpatient clinic of the university institute of psychiatry and AD | The Resilience Scale |
140.6 (17.2) |
In persons with mild and moderate AD, caregiver resilience was inversely related to emotional problems. There was no difference between resilience in caregivers of people with mild versus moderate AD. In the mild AD group, neuropsychiatric symptoms of the person with AD and caregiver's depressive symptoms were related to caregiver resilience. In the moderate AD group, caregiver QOL and coresiding with the care‐recipient were related to resilience |
Chan et al. (2019) 83 | To explore caregiver strain and resilience of caregivers of patients with AD in Malaysia; to determine factors associated with caregiver strains in caregivers of patients with AD; and to determine the effect of resilience on the relationship between caregiver strains and caregiver or patient factors | AD Foundation Malaysia | The Brief Resilience Scale |
19.2 (3.3) |
The sample demonstrated moderate to high resilience. Resilience was associated with gender and employment status. A negative correlation was found between resilience and caregiver strain |
Dias et al. (2016) 89 | To investigate the relationship between resilience and sociodemographic and clinical factors of people with dementia; to test the hypothesis that caregivers' resilience is a personality trait, independent from the clinical symptoms of the person with dementia | Physicians' referral from a dementia outpatient clinic | The Resilience Scale |
137.6 (15.5) |
Participants reported moderate to high levels of resilience. Resilience was not related to gender, clinical or emotional problems. Resilience was related to caregiver QOL, and inversely associated with depressive symptoms. There was no relationship between caregivers' resilience and sociodemographic and clinical characteristics of people with dementia. The authors concluded that resilience is an individual characteristic |
Serra et al. (2018) 65 | To investigate a set of caregiver and patient factors, such as psychosocial protective variables, linked to abuse‐related behaviour of PWD | Referrals from the associations of relatives of PWD, neurology outpatient clinics and The National Reference Centre of AD | The Connor–Davidson Resilience Scale |
73.9 (13.7) |
Resilience and social support were negatively associated with abuse scores (i.e., protective effect). Social support and resilience were associated with a lower probability of abuse |
Sutter et al. (2016) 47 | To examine the relationships between personal strengths (optimism, sense of coherence and resilience) and mental health of dementia caregivers from Latin America | Regional neuroscience institute and university, local neurology outpatient clinics, flyers, word‐of‐mouth, local community connections | The Brief Resilience Scale | 17.4 (5.6) | More manageability, general resilience and social competence were uniquely associated with lower depression. Resilience and other variables were not predictive of caregiver burden or life satisfaction |
Jones et al. (2018) 48 | To describe the demographic and psychosocial characteristics of caregivers who attend dementia cafes and to identify which factors influence the likelihood of family caregivers attending dementia cafes | Dementia cafes and health and well‐being events facilitated by local AD or well‐being societies | The Brief Resilient Coping Scale | NR | Caregivers who attended cafes reported higher resilience and subjective well‐being; no difference in social support was detected |
Jones, Killett et al. (2019a) 55 ; Jones, Woodward et al. (2019b) 49 | 2019a | Adverts in newsletters, carer information events held by local charities and an online carer's forum, dementia cafes | The Brief Resilient Coping Scale | NRa | 2019a |
To investigate factors that affect resilient coping in carers; to assess whether symptoms of distress vary between carers with differing levels of resilient coping; and to identify whether resilient coping acts as a mediator in the carer distress–well‐being relationship | ‘High’ resilient carers reported less distress than ‘low’ resilient carers. Resilient coping partially mediated the relationships between well‐being and caregiver distress (i.e., depression, anxiety, stress and burden). Carers with high resilient coping skills reported less depression, anxiety, stress and burden than those with ‘low’ resilient coping | ||||
2019b | 2019b | ||||
To compare sociodemographic characteristics and the availability of social support for carers with ‘low’ and ‘high’ resilient coping and to identify if social support predicted high resilient coping in informal carers of people with dementia | The availability of emotional/informational support was most likely to predict resilient coping and tangible support was the least likely to predict resilient coping. Only gender predicted high resilient coping. No single domain of social support had a greater influence on resilient coping | ||||
Wilks et al. (2011, 2018) 80 , 81 ) | 2011 | Mailing lists from a nonprofit AD services organisation; African American communities (e.g., churches, community centres, adult day centres, a home health agency, caregiver homes) | The Shortened Resilience Scale | 2011 | 2011 |
This study assessed the impact of AD patients' aggressive behaviour (i.e., AD aggression) on caregiver coping strategies (task‐, emotion‐, and avoidance‐focused) and caregiver resilience, and examined whether a coping strategy moderated the AD aggression–caregiver resilience relationship | 5.9c | Aggression negatively predicted caregiver resilience. All coping strategies correlated with resilience scores. Task‐focused coping was positively related to resilience. Emotion and avoidance‐focused coping strategies separately interacted with aggression and increased their negative relationship with resilience. Task‐focused coping showed no moderating effect | |||
2018 | 2018 | 2018 | |||
To understand whether spiritual support with AD caregivers acts as a moderating factor among the caregiving burden–resilience relationship in a manner similar to caregiver social support, and to observe ethnicity, African American versus Caucasian caregivers, in said moderation | 5.8c | For each ethnic group of caregivers, burden was inversely proportional to resilience. In all groups, the association between spiritual support and resilience was positive and direct. Social support did not moderate risk within either group. African American caregivers reported higher resilience than their Caucasian counterparts | |||
Wilks (2008a) 66 ; Wilks and Croom (2008b) 82 | 2008a | Two large AD care conferences: one held in a large urban area and another held in a rural locale | The Shortened Resilience Scale |
5.5 (1.3) |
2008a |
To evaluate psychometric properties of the shortened Resilience Scale among a sample of AD caregivers | Results confirmed the RS15 to be a psychometrically sound measure that can be used to appraise the efficacy of caregiving adaptability among the sample | ||||
2008b | 2008b | ||||
To examine whether social support functions as a protective, resilience factor among AD caregivers; to examine the relationship between risk (i.e., perceived stress) to mental and physical health, an outcome of resilience and potential protective factors for resilience among caregivers | The sample reported moderate to high resilience. Perceived stress negatively influenced resilience and accounted for 43% of variance in resilience scores. Social support positively influenced resilience, and caregivers with high family support had the highest probability of elevated resilience. Social support is a protective mediator of resilience | ||||
Anderson et al. (2019) 92 | To integrate related explanatory (personality, coping) and mediating (hope, resilience, self‐efficacy) and caregiver outcome (burden, psychological distress, quality of life) variables into a larger model and to test the role of resilience, hope and self‐efficacy among family caregivers of persons with TBI | Six regional inpatient and community rehabilitation centres | The Connor–Davidson Resilience Scale |
76.23 (12.3) |
The model accounted for 63% of the variance in resilience. Resilience had a direct effect on positive affect in caregivers. There was a strong positive association between general self‐efficacy and resilience. Problem‐focused coping had a direct positive effect on resilience. Resilience was indirectly associated with caregiver burden when mediated through social support. Resilience demonstrated a direct effect on hope that is associated with positive mental health. Resilience was associated with reduced morbidity |
Hayas et al. (2015) 50 | To develop the Questionnaire of Resilience in Caregivers of Acquired Brain Injury (QRC‐ABI) and explore its psychometric properties | The Federation of ABI Associations and public day care centres specializing in ABI | QRC‐ABI |
43.24 (11.3) |
The QRC‐ABI showed good reliability and validity. Convergent validity was supported through positive correlations of the QRC‐ABI with QOL, positive aspects of caregiving and posttraumatic growth and a negative correlation with perceived burden |
Vatter et al. (2018, 2020) 56 , 57 | 2018 | Nation‐wide post or as part of a larger study (ref) | The Brief Resilience Scale |
24.97 (11.9) |
2018 |
To explore the factor structure of the Zarit Burden Interview (ZBI) in life partners of people with Parkinson's‐related dementia and to examine the relationships among the emerging factors and the demographic and clinical features | Five factors of the ZBI (i.e., social and psychological constraints, personal strain, interference with personal life, concerns about future and guilt) all negatively correlated with resilience. Lower resilience and higher negative strain and feelings of resentment were contributors to burden | ||||
2020 | 2020 | ||||
To explore and compare levels of mental health, care burden and relationship satisfaction among caregiving spouses of people with mild cognitive impairment or dementia in PD (PDD) or dementia with Lewy bodies (DLB) | Over 75% of respondents reported good resilience. ZBI scores correlated with resilience. Caregivers who were dissatisfied with their relationship reported lower resilience. Burden, stress, resilience, relationship satisfaction, quality of life, anxiety, depression and mental health levels did not differ between spouses of people with PDD and DLB. | ||||
Ledbetter et al. (2020) 67 | To investigate how individual and contextual factors (i.e., caregiving tasks, resilience, timing of the SCI) moderate the extent to which receiving social support predicts psychosocial distress among SCI caregiving romantic partners | Online groups targeted at SCI caregivers | The Brief Resilience Scale |
4.05 (0.8) |
Resilience inversely predicted psychosocial distress in both the preinjury and postinjury groups. Findings revealed the benefits of resilience. Receiving high‐quality support and timing of the injury moderated resilience effects. Injuries sustained after relationship initiation threatened well‐being and closeness and altered the extent to which support and resilience were associated with health and relationship benefits |
O'Rourke et al. (2010) 68 | To examine the three facets of psychological resilience (i.e., perceived control, commitment to living, challenge versus stability) as predictors of depressive symptoms over time among spousal caregivers of PwAD | Clinic for AD and related disorders at a regional university hospital | The Dispositional Resilience Scale | NR | Resilience was associated with depressive symptoms among caregivers. Challenge and perceived control predicted depressive symptoms 1 year later. An increase in challenges over time predicted lower levels of depressive symptoms at Time 2. Commitment was not associated with depressive symptoms at any time point |
Rivera‐Navarro et al. (2018) 51 | To validate the Caregiver Abuse Screen (CASE) as an instrument for detecting the maltreatment of people with dementia in Spain | Local associations of relatives of people with AD and other dementia and neurology outpatient clinics | The Connor–Davidson Resilience Scale |
73.6 (13.4) |
High CASE scores were associated with greater burden, lower social support and lower resilience of caregivers. Resilience scores were negatively correlated with interpersonal abuse and neglect/dependency. The consistent negative association of CASE scores with resilience is indicative of this advantageous characteristic |
Tyler et al. (2020) 69 | To validate a theoretical structural equation model whereby social support is associated with higher levels of resilience in PD caregivers and increased resilience is related to decreased mental health symptoms | PD clinics associated with academic university institutions in Mexico and the PD and Movement Disorders Center at a regional medical centre in the USA | The Brief Resilience Scale | NR | The model explained 11% of the variance in resilience. Higher levels of social support were associated with higher resilience, which in turn was associated with lower mental health symptoms. Resilience partially mediated the effect of social support on mental health symptoms |
Quantitative, intervention studies (n = 4) | |||||
Ghaffari et al. (2019) 84 | To determine the effectiveness of resilience education in the mental health of family caregivers of elderly patients with AD | Referrals from regional hospital and neurologist offices | The Connor–Davidson Resilience Scale | NR | Resilience education promoted the mental health of family AD caregivers by decreasing somatic symptoms and social dysfunction |
Lavretsky et al. (2010) 75 | To examine the potential of an antidepressant drug (escitalopram) to improve depression, resilience to stress and quality of life in family dementia caregivers in a randomized placebo‐controlled double‐blinded trial | NR | The Connor–Davidson Resilience Scale |
60.2 (16.7) |
Measures of depression, anxiety, resilience, burden and distress and quality of life improved on escitalopram compared with placebo groups |
MacCourt et al. (2017) 70 | To assess the structure and effectiveness of a grief management coaching intervention with caregivers of individuals with dementia | Local social media and referrals from regional AD society | The Resilience Scale |
Spouse T1: 67.9c T2: 68.9c |
For the intervention group, grief, coping, empowerment and resilience scores improved postintervention. The intervention group showed greater resilience at Time 2. Time 1 resilience scores predicted greater resilience at Time 2 |
Adult child T1: 66.6c T2: 71.1c |
|||||
Pandya (2019) 85 | To report the impact of a long‐term meditation programme for enhancing self‐efficacy and resilience of home‐based caregivers of older adults with AD | Network of agencies linked to older adults, geriatric clinics and units in private hospitals | The Resilience Scale for Adults; The Caregiver Resilience Scale (CRS) |
RSA Control Pre: 99.2 (8.3) Post: 100 (8.3) Intervention Pre: 100.31 (9) Post:187.93 (14.2) |
Posttest RSA and CRS scores of the intervention group were higher than the control group and their own pretest scores. Caregiver women, spouses, Hindus, middle class, with college and higher education, homemakers, who attended at least 75% of the meditation lessons and regularly practiced meditation at home reported lower posttest perceived caregiving burden, higher self‐efficacy and resilience. Meditation was effective for increasing resilience |
CRS Control Pre: 30.28 (4.4) Post: 31.03 (5.3) Intervention Pre: 31.21 (4.9) Post: 58.71 (6.8) |
|||||
Mixed‐methods studies (n = 4) | |||||
Maneewat et al. (2016) 86 | To develop the CRS for Thai caregivers of older persons with dementia and to examine its validity and reliability | Memory Clinic, Neurological Clinic or Geriatric Clinic in the Outpatient Department at a regional hospital | The CRS; semi‐structured interviews | NR | The final version of the CRS was composed of 30 items within six domains: physical competence; relationship competence; emotional competence; cognitive competence; moral competence; and spiritual competence. The 30‐item CRS was considered a valid and reliable instrument |
Bull (2014) 71 | To describe family caregivers' level of resilience and psychological distress and to describe the strategies that family caregivers use to persevere in their caregiving role despite the challenges encountered in caring for a family member with dementia | Five adult day centres located in a city setting | The Resilience Scale; narrative interviews |
154.3 (15.8) |
Participants had high resilience and low psychological distress. The use of self‐sustaining strategies explained the high scores on resilience and low levels of psychological distress. Caregivers used four strategies to sustain the self: drawing on past life experiences that dealt with difficult situations, nourishing the self, relying on spirituality and seeking dementia‐related information |
Jones et al. (2019) 54 | To explore discrepancies and congruency between definitions of resilience in the academic literature and carers' own conceptualizations; to assess differences and similarities in conceptualizations of resilience between carers with high‐, medium‐ and low‐resilience scores; and to compare carers' perceived level of resilience with the level of resilience when measured on a standardized tool | Theoretical sampling recruited from participants in previous study 48 | Brief Resilient Coping Scale; semi‐structured interviews | NR | Under half (46%) of the carers had low resilience. Carers' definitions of resilience were concordant with clinical and academic definitions; however, they extended the concept and placed greater value on the role of self‐compassion. Carers recognized that the appearance of resilience may have negative consequences in terms of securing support from others. Resilience scores did not always match carers' own perceptions of their level of resilience |
Kidd et al. (2011) 72 | To test the effectiveness of a poetry writing intervention for family caregivers of elders with dementia and to examine outcome variables of self‐transcendence, resilience, depressive symptoms and subjective caregiver burden | Support groups, churches and agencies | The Resilience Scale; interviews | NR | Women were lower in self‐transcendence and resilience, and higher in depressive symptoms and burden. Older caregivers scored higher than younger caregivers on the study variables of self‐transcendence and resilience. Poetry writing was an effective intervention that may promote resilient outcomes |
Qualitative studies (n = 7) | |||||
---|---|---|---|---|---|
Author (year) | Purpose | Recruitment setting | Means of resilience assessment | Key results | |
Bekhet and Avery (2018) 19 | To identify components of resilience theory (i.e., risk factors, protective factors, overlapping factors) from the perspective of caregivers of PWD | Regional AD Association early stage programmes | Open‐ended questions on written questionnaires | The experience of dementia caregiving involved a combination of risk factors and protective factors, suggesting that caregivers may feel conflicted. Risk factors included experiences of stress and difficulties, demanding tasks, frustration, lack of social support, exhaustion and negative feelings. Protective factors included feeling rewarded and serving a purpose. If protective factors were more predominant, then caregivers became more resilient and experienced associated positive health outcomes | |
Roberts and Struckmeyer (2018) 73 |
To examine family caregiver perspectives on how respite programming impacts their resilience and ability to better handle the demands of their responsibilities |
Recruited as part of a larger studyb through respite providers | Semi‐structured interviews | Several themes emerged describing the path to caregiver resilience that included family dynamics, isolation, financial struggles, seeking respite and acceptance. The road to acceptance became a critical factor in the development of resilience | |
Han et al. (2019) 25 | To identify challenges, possible solutions as resources for resilience and expected consequences from the perspective of family caregivers of hospice patients with dementia | Two large hospice agencies recruited as part of a larger clinical trial | Deductive content analysis of secondary clinical trial data | Resilience resources were identified at the individual, community and societal levels. Resources included knowledge, self‐control and appraisal, self‐care, using visual materials, having options to choose a good care facility with exemplary providers, family or friends' support, involvement in volunteer activities, legislative support, public awareness and health insurance. Identified challenges were difficulties in communication, providing care and decision‐making, lack of knowledge, emotional challenges, concern about care facility selection, death with dignity and lack of public awareness | |
Liu et al. (2020) 74 | To investigate the resilience of a growing but largely underserved and understudied population—Chinese American dementia caregivers, whose experience is embedded in their development throughout the life span, process of migration and sociocultural contexts | Local agency providing services for dementia caregivers with a representation of Chinese clients | Semi‐structured interviews | Main themes fit within two categories, challenge and resilience, in each of the four principles—time and place, timing in lives, linked lives and agency—of the developmental life course perspective. Physical and emotional exhaustion was the most frequently mentioned challenge theme, followed by limited knowledge of dementia, navigating the healthcare system and limited time for self‐development. Three aspects of resilience—sense of mastery, access to formal and informal support and commitment to care—were salient among caregivers | |
Donnellan et al. (2015, 2017, 2019) 38 , 52 , 53 | 2015 | Two local dementia support groups and a care home | Semi‐structured interviews | 2015 | |
To assess whether spousal dementia carers can achieve resilience and to reveal which factors and resources facilitate or hinder resilience within the ecological framework | Carers achieve resilience via a complex multidimensional process. A resilient carer was someone who stayed positive, who maintained their relationship with their loved one's former self, who were knowledgeable, well supported and who were engaged with respite services. Facilitating community factors included friendships with common experience and social participation. Individual hindering resilience factors were negative outlook and perceived social isolation | ||||
2017 | 2017 | ||||
To explore social support as a key component of resilience and to identify the availability and function of support provided to older spousal dementia carers | Social support is not always sufficient to facilitate resilience, as negative perceptions of support may moderate the effect of support on resilience. Family and friends served a wide range of functions, but were equally available to resilient and nonresilient participants | ||||
2019 | 2019 | ||||
To use qualitative longitudinal methods to examine trajectories of resilience and which assets and resources are associated with resilience and care status transitions in spousal dementia carers | Five participants remained resilient, three remained nonresilient and four participants became resilient. Only one participant became nonresilient. Stable resilience was characterized by continuing individual assets and community resources. Carers who became resilient returned to previous resources or gained new resources |
Abbreviations: ABI, acquired brain injury; AD, Alzheimer's disease; CRS, caregiver resilience scale; MND, motor neuron disease; NIV, noninvasive ventilation; NR, not reported; PD, Parkinson's disease; PWD, persons with dementia; QOL, quality of life; RSA, resilience scale for adults; SCI, spinal cord injury; SMV, service member veteran; TBI, traumatic brain injury.
Authors divided participants into ‘low’ (BRCS 0–13), ‘medium’ (BRCS 14‐16) and ‘high’ (BRCS 17+) resilient groups, with no inclusion of the total mean resilience scores.
Reference for a large study not provided.
SD for resilience scores not reported.