Skip to content

Toggle service links

You are here

  1. Home
  2. Stress

Stress

Distress relief

Reports on research from the Social Policy Research Unit (SPRU) designed to measure and monitor health inequalities between carers and noncarers. The study used data from the British Household Panel Survey (BHPS) covering the period from 1991 to 2000. Results found that emotional and mental health problems are more often associated with caregiving than physical health problems

Thu, 07/20/2017 - 15:12

Correlates of stress in carers

BACKGROUND: Mental health services are required to take account of the needs of carers, yet little is known about how services affect carers.

AIMS: This paper explores the relationship between the user's mental health problems, the services received and the impact of caring on carers.

METHODS: Sixty-four carers were interviewed, measuring their experiences of care-giving, carer stress and the service user's level of impairment. A robust, composite measure of user severity was derived.

Thu, 07/20/2017 - 15:12

Predictors of high level of burden and distress in caregivers of demented patients: results of an Italian multicenter study

Considerable suffering is experienced by carers of patients with dementia. Most existing studies do not consider the coexistence of subjective and objective aspects that cause, interacting to each other, this suffering. The authors: (1) define the high-risk group of caregivers on the bases of the scores obtained on the four scales evaluating burden, distress, depression and anxiety (BDDA) taken into account simultaneously and (2) evaluate risk factors related to the high level of BDDA. 419 elderly outpatients with dementia and their caregivers were enrolled.

Thu, 07/20/2017 - 15:12

Stroke caregivers' strain prevalence and determinants in the first six months after stroke

PURPOSE: Many disabled stroke survivors live at home supported by informal caregivers. Research has revealed that these caregivers are experiencing strain. This study aims to examine the prevalence and differences over time of caregivers' strain in the first 6 months post-stroke and to predict caregiver strain based on patients' and caregivers' characteristics and service input.

Thu, 07/20/2017 - 15:12

Alzheimer's disease: the psychological and physical effects of the caregiver's role, part 2

The purpose of this study was to investigate the physical and psychological effects on informal caregivers of looking after a person with Alzheimer’s disease. A descriptive survey was conducted in counties Galway, Mayo and Roscommon in Ireland using a simple random sample of caregivers registered with the Alzheimer Society of Ireland, Galway, or the Western Alzheimer’s Foundation. The findings from the study show that a significant proportion of caregivers reported poor self-rated health and depression. Restless sleep and a decreased tolerance for pain were also common.

Thu, 07/20/2017 - 15:12

Grandmothers and caregiving to grandchildren: continuity, change, and outcomes over 24 months

Purpose: Transitions in caregiving, such as becoming a primary caregiver to grandchildren or having adult children and grandchildren move in or out, may affect the well-being of the grandmother. Design and Methods: This report describes caregiving patterns at 3 time points over 24 months in a sample of 485 Ohio grandmothers and examines the effects of stability and change in grandmother caregiving roles (raising a grandchild, living in a multigenerational home, or not caregiving to grandchildren).

Thu, 07/20/2017 - 15:12

An interpretive phenomenological account of the experiences of family carers of the elderly

Research on family caregiving has focused on the quantitative as opposed to the qualitative investigation of the impact of caregiving on the health and psychological well-being of family carers. In this study, interpretive phenomenological analysis (IPA) was used to explore the subjective experience, needs and appraisals from the perspectives of family carers of older adults. Six family carers were recruited from a carer support group; one male and five female primary carers to an elderly family member with age or disease-related impairment.

Thu, 07/20/2017 - 15:11

Stress factors and mental health of carers with relatives suffering from schizophrenia in Hong Kong: implications for culturally sensitive practices

Based on Spaniol and Jung's stress and coping framework (1993), this study examined the difficulties and stresses experienced by carers with relatives suffering from schizophrenia in Hong Kong. The impact of these difficulties and stresses and of mastery as a coping resource on carers' mental health was also explored. Results show that carers experience most difficulties and stresses related to the management of negative symptoms such as refusal to perform household duties and neglect of personal hygiene, and less to handling positive symptoms such as bizarre behaviours and thoughts.

Thu, 07/20/2017 - 15:11

Depression as a mediator: viewing caregiver well-being and strain in a different light

This study examines the relationship between caregiver characteristics and caregiver well-being as comprised of two components, activities of living and basic needs. The role of depression in predicting caregiver well-being is explored using a sample of caregivers of family members with chronic illness. Using a path-analysis model, multivariate findings suggest that depression explains 56% of the variance in activities of living and 64% in basic needs. Path analysis further identifies depression as a mediator between stress and well-being.

Thu, 07/20/2017 - 15:11

Coping and subjective burden in caregivers of older relatives: a quantitative systematic review

Aim.  This article is a report on a review of the effect of coping strategies on subjective burden in informal caregivers of older adults.

Background.  Informal care has negative effects on caregivers’ health, and subjective burden is one of these. It has been linked with other effects (e.g. anxiety and depression). Thus, greater prevention of subjective burden will mean increased prevention of these effects. To achieve this, identification of factors related to subjective burden is essential.

Thu, 07/20/2017 - 15:11