An investigation into the construct validity of the Carer Experience Scale (CES)

[1]  B. Kaambwa,et al.  The inclusion of informal care in applied economic evaluation: a review. , 2012, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.

[2]  W. Brouwer,et al.  Sustained informal care: The feasibility, construct validity and test–retest reliability of the CarerQol-instrument to measure the impact of informal care in long-term care , 2011, Aging & mental health.

[3]  J. Coast,et al.  QALYs and Carers , 2011, PharmacoEconomics.

[4]  H. Doll,et al.  Does self-reported well-being of patients with Parkinson's disease influence caregiver strain and quality of life? , 2011, Parkinsonism & related disorders.

[5]  Joanna Coast,et al.  Estimation of a Preference-Based Carer Experience Scale , 2011, Medical decision making : an international journal of the Society for Medical Decision Making.

[6]  W. Brouwer,et al.  A new test of the construct validity of the CarerQol instrument: measuring the impact of informal care giving , 2011, Quality of Life Research.

[7]  W. Brouwer,et al.  The inclusion of positive aspects of caring in the Caregiver Strain Index: tests of feasibility and validity. , 2010, International journal of nursing studies.

[8]  W. Brouwer,et al.  Caring for and caring about: disentangling the caregiver effect and the family effect. , 2010, Journal of Health Economics.

[9]  Joanna Coast,et al.  What do people value when they provide unpaid care for an older person? A meta-ethnography with interview follow-up. , 2008, Social science & medicine.

[10]  W. Brouwer,et al.  The CarerQol instrument: A new instrument to measure care-related quality of life of informal caregivers for use in economic evaluations , 2006, Quality of Life Research.

[11]  W. Brouwer Too important to ignore , 2006, PharmacoEconomics.

[12]  M. Koopmanschap,et al.  Process utility from providing informal care: the benefit of caring. , 2005, Health policy.

[13]  S. Kwon,et al.  Factors affecting the burden on caregivers of stroke survivors in South Korea. , 2005, Archives of physical medicine and rehabilitation.

[14]  M. Koopmanschap,et al.  Burden of Informal Caregiving for Stroke Patients , 2005, Cerebrovascular Diseases.

[15]  A. Barnett,et al.  Caregiver burden, time spent caring and health status in the first 12 months following stroke , 2005, Brain injury.

[16]  V. Tomassini,et al.  Relationship between emotional distress in caregivers and health status in persons with multiple sclerosis , 2004, Multiple sclerosis.

[17]  M. Koopmanschap,et al.  What really matters: an inquiry into the relative importance of dimensions of informal caregiver burden , 2004, Clinical rehabilitation.

[18]  M. Koopmanschap,et al.  Instruments for assessing the burden of informal caregiving for stroke patients in clinical practice: a comparison of CSI, CRA, SCQ and self-rated burden , 2004, Clinical rehabilitation.

[19]  M. Kane Current Concerns in Validity Theory , 2001 .

[20]  R. Sanderman,et al.  Risk factors for burn-out in caregivers of stroke patients, and possibilities for intervention , 2001, Clinical rehabilitation.

[21]  J. Grant,et al.  Sociodemographic, physical, and psychosocial characteristics of depressed and non-depressed family caregivers of stroke survivors. , 2000, Brain injury.

[22]  Adelina Comas-Herrera,et al.  Relying on informal care in the new century? Informal care for elderly people in England to 2031 , 2000, Ageing and Society.

[23]  P. Neumann,et al.  MEASURING COSTS IN COST-UTILITY ANALYSES , 2000, International Journal of Technology Assessment in Health Care.

[24]  C. Bugge,et al.  Stroke patients' informal caregivers. Patient, caregiver, and service factors that affect caregiver strain. , 1999, Stroke.

[25]  M. Limburg,et al.  The burden of caregiving in partners of long-term stroke survivors. , 1998, Stroke.

[26]  S. Orbell,et al.  Measuring the impact of informal caring , 1993 .

[27]  N. Vetter,et al.  Formal and informal support received by carers of elderly dependents. , 1985, British medical journal.

[28]  S. Zarit,et al.  Relatives of the impaired elderly: correlates of feelings of burden. , 1980, The Gerontologist.

[29]  B. Winblad,et al.  Caring for a demented elderly person--burden and burnout among caregiving relatives. , 1997, Journal of advanced nursing.

[30]  Judith G. Gonyea,et al.  Caregiving and the experience of subjective and objective burden. , 1985 .

[31]  L. Cronbach,et al.  Construct validity in psychological tests. , 1955, Psychological bulletin.