SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    PAMELA ROACH, JOHN KEADY, PENNY BEE, SION WILLIAMS, ‘We can't keep going on like this’: identifying family storylines in young onset dementia, Ageing and Society, 2014, 34, 08, 1397

    CrossRef

  2. 2
    Michael J. Sheridan, Jeronda Burley, Danetta E. Hendricks, Theda Rose, “Caring for One's Own”: Variation in the Lived Experience of African-American Caregivers of Elders, Journal of Ethnic And Cultural Diversity in Social Work, 2014, 23, 1, 1

    CrossRef

  3. 3
    Jennifer R. Day, Ruth A. Anderson, Linda L. Davis, Compassion Fatigue in Adult Daughter Caregivers of a Parent with Dementia, Issues in Mental Health Nursing, 2014, 35, 10, 796

    CrossRef

  4. 4
    Heejung Kim, Karen M. Rose, Concept analysis of family homeostasis, Journal of Advanced Nursing, 2014, 70, 11
  5. 5
    Susanne van den Hooff, Anne Goossensen, Conflicting Conceptions of Autonomy: Experiences of Family Carers with Involuntary Admissions of their Relatives, Ethics and Social Welfare, 2014, 1

    CrossRef

  6. 6
    Katrin M. Seeher, Lee-Fay Low, Simone Reppermund, Melissa J. Slavin, Brian M. Draper, Kristan Kang, Nicole A. Kochan, Julian N. Trollor, Perminder S. Sachdev, Henry Brodaty, Correlates of psychological distress in study partners of older people with and without mild cognitive impairment (MCI) – the Sydney Memory and Ageing Study, Aging & Mental Health, 2014, 18, 6, 694

    CrossRef

  7. 7
    C. L. Campbell, S. McCoy, N. Hoffman, P. O'Neil, Decreasing Role Strain for Caregivers of Veterans with Dependence in Performing Activities of Daily Living, Health & Social Work, 2014, 39, 1, 55

    CrossRef

  8. 8
    Hülya Yıkılkan, Cenk Aypak, Süleyman Görpelioğlu, Depression, Anxiety and Quality of Life in Caregivers of Long-Term Home Care Patients, Archives of Psychiatric Nursing, 2014, 28, 3, 193

    CrossRef

  9. 9
    Unchulee Taemeeyapradit, Dussadee Udomittipong, Sawitri Assanangkornchai, Development of a burden scale for caregivers of dementia patients, Asian Journal of Psychiatry, 2014, 8, 22

    CrossRef

  10. 10
    Evridiki Papastavrou, Panayiota Andreou, Nicos Middleton, Savvas Papacostas, Irini Kyriacou Georgiou, Factors associated with quality of life among family members of patients with dementia in Cyprus, International Psychogeriatrics, 2014, 26, 03, 443

    CrossRef

  11. 11
    Jing Wang, Lily Dongxia Xiao, Guo-Ping He, Shahid Ullah, Anita De Bellis, Factors contributing to caregiver burden in dementia in a country without formal caregiver support, Aging & Mental Health, 2014, 18, 8, 986

    CrossRef

  12. 12
    Cindy C. Wong, Margaret I. Wallhagen, Family Caregivers of Individuals with Frontotemporal Dementia: Examining the Relationship Between Coping and Caregiver Physical and Mental Health, Journal of Gerontological Nursing, 2014, 40, 1, 30

    CrossRef

  13. 13
    Wendy Moyle, Marie Louise Cooke, Elizabeth Beattie, David H.K. Shum, Siobhan T. O’Dwyer, Sue Barrett, Foot massage versus quiet presence on agitation and mood in people with dementia: A randomised controlled trial, International Journal of Nursing Studies, 2014, 51, 6, 856

    CrossRef

  14. 14
    Scott S. Hall, Jayanthi Kandiah, Diana Saiki, Jinhee Nam, Amy Harden, Soonjee Park, Implications of Smart Wear Technology for Family Caregiving Relationships: Focus Group Perceptions, Social Work in Health Care, 2014, 53, 10, 994

    CrossRef

  15. 15
    Laurence M. Solberg, Lauren B. Solberg, Emily N. Peterson, Measuring Impact of Stress in Sandwich Generation Caring for Demented Parents, GeroPsych: The Journal of Gerontopsychology and Geriatric Psychiatry, 2014, 27, 4, 171

    CrossRef

  16. 16
    Pia Muders, Corinna Aruna Zahrt-Omar, Sonja Bussmann, Julia Haberstroh, Martin Weber, Support for families of patients dying with dementia: A qualitative analysis of bereaved family members' experiences and suggestions, Palliative and Supportive Care, 2014, 1

    CrossRef

  17. 17
    Vidyalakshmi Sundar, Susan W. Fox, Kimberly G. Phillips, Transitions in Caregiving: Evaluating a Person-Centered Approach to Supporting Family Caregivers in the Community, Journal of Gerontological Social Work, 2014, 57, 6-7, 750

    CrossRef

  18. 18
    Marta E. Pagán-Ortiz, Dharma E. Cortés, Noelle Rudloff, Patricia Weitzman, Sue Levkoff, Use of an Online Community to Provide Support to Caregivers of People With Dementia, Journal of Gerontological Social Work, 2014, 57, 6-7, 694

    CrossRef

  19. 19
    Chloé Gervès-Pinquié, Martine M Bellanger, Joel Ankri, Willingness to pay for informal care in France: the value of funding support interventions for caregivers, Health Economics Review, 2014, 4, 1, 34

    CrossRef

  20. 20
    Louise Daly, Mary McCarron, Agnes Higgins, Philip McCallion, ‘Sustaining Place’ – a grounded theory of how informal carers of people with dementia manage alterations to relationships within their social worlds, Journal of Clinical Nursing, 2013, 22, 3-4
  21. 21
    Vasiliki Orgeta, Elena Lo Sterzo, Martin Orrell, Assessing mental well-being in family carers of people with dementia using the Warwick–Edinburgh Mental Well-Being Scale, International Psychogeriatrics, 2013, 25, 09, 1443

    CrossRef

  22. 22
    Yueh-Mei Gau, Petra Buettner, Kim Usher, Lee Stewart, Burden experienced by community health volunteers in Taiwan: a survey, BMC Public Health, 2013, 13, 1, 491

    CrossRef

  23. 23
    Xue Bai, Timothy C. Y. Kwok, Natalie Y. T. Chan, Florence K. Y. Ho, Determinants of job satisfaction in foreign domestic helpers caring for people with dementia in Hong Kong, Health & Social Care in the Community, 2013, 21, 5
  24. 24
    Abir K. Bekhet, Effects of positive cognitions and resourcefulness on caregiver burden among caregivers of persons with dementia, International Journal of Mental Health Nursing, 2013, 22, 4
  25. 25
    Laurie A. Miller, Eneida Mioshi, Sharon Savage, Suncica Lah, John R. Hodges, Olivier Piguet, Identifying Cognitive and Demographic Variables That Contribute to Carer Burden in Dementia, Dementia and Geriatric Cognitive Disorders, 2013, 36, 1-2, 43

    CrossRef

  26. 26
    George J. Demakis, Neuropsychological Evaluation of Decision-Making Capacity in Older Adults, Psychological Injury and Law, 2013, 6, 1, 41

    CrossRef

  27. 27
    Jenny Alwin, Jan Persson, Barbro Krevers, Perception and significance of an assistive technology intervention – the perspectives of relatives of persons with dementia*, Disability and Rehabilitation, 2013, 35, 18, 1519

    CrossRef

  28. 28
    Ruth Palan Lopez, A.J. Guarino, Psychometric Evaluation of the Surrogate Decision Making Self-Efficacy Scale, Research in Gerontological Nursing, 2013, 6, 1, 71

    CrossRef

  29. 29
    Vasiliki Orgeta, Elena Lo Sterzo, Sense of coherence, burden, and affective symptoms in family carers of people with dementia, International Psychogeriatrics, 2013, 25, 06, 973

    CrossRef

  30. 30
    Hayley Robinson, Bruce A. MacDonald, Ngaire Kerse, Elizabeth Broadbent, Suitability of Healthcare Robots for a Dementia Unit and Suggested Improvements, Journal of the American Medical Directors Association, 2013, 14, 1, 34

    CrossRef

  31. 31
    Anders Wimo, Linus Jönsson, John Bond, Martin Prince, Bengt Winblad, The worldwide economic impact of dementia 2010, Alzheimer's & Dementia, 2013, 9, 1, 1

    CrossRef

  32. 32
    Merle E. Mast, To Use or Not to Use: A Literature Review of Factors that Influence Family Caregivers’ Use of Support Services, Journal of Gerontological Nursing, 2013, 39, 1, 20

    CrossRef

  33. 33
    Ourania Govina, Grigorios Kotronoulas, Kyriaki Mystakidou, Margarita Giannakopoulou, Antonios Galanos, Elisabeth Patiraki, Validation of the revised Bakas Caregiving Outcomes Scale in Greek caregivers of patients with advanced cancer receiving palliative radiotherapy, Supportive Care in Cancer, 2013, 21, 5, 1395

    CrossRef

  34. 34
    Hyunjin Oh, Karen G. Schepp, Wives Becoming Caregivers, Journal of Hospice & Palliative Nursing, 2013, 15, 4, 244

    CrossRef

  35. 35
    P. ROACH, J. KEADY, P. BEE, ‘It's easier just to separate them’: practice constructions in the mental health care and support of younger people with dementia and their families, Journal of Psychiatric and Mental Health Nursing, 2012, 19, 6
  36. 36
    Chiara Zucchella, Michelangelo Bartolo, Chiara Pasotti, Laura Chiapella, Elena Sinforiani, Caregiver Burden and Coping in Early-stage Alzheimer Disease, Alzheimer Disease & Associated Disorders, 2012, 26, 1, 55

    CrossRef

  37. 37
    José María García-Alberca, Belén Cruz, José Pablo Lara, Victoria Garrido, Esther Gris, Almudena Lara, Concepción Castilla, Disengagement coping partially mediates the relationship between caregiver burden and anxiety and depression in caregivers of people with Alzheimer's disease. Results from the MÁLAGA-AD study, Journal of Affective Disorders, 2012, 136, 3, 848

    CrossRef

  38. 38
    Ruth Landau, Shirli Werner, Ethical aspects of using GPS for tracking people with dementia: recommendations for practice, International Psychogeriatrics, 2012, 24, 03, 358

    CrossRef

  39. 39
    Anelia Mitseva, Carrie Beth Peterson, Christina Karamberi, Lamprini Ch. Oikonomou, Athanasios V. Ballis, Charalampos Giannakakos, George E. Dafoulas, Gerontechnology: Providing a Helping Hand When Caring for Cognitively Impaired Older Adults—Intermediate Results from a Controlled Study on the Satisfaction and Acceptance of Informal Caregivers, Current Gerontology and Geriatrics Research, 2012, 2012, 1

    CrossRef

  40. 40
    Evridiki Papastavrou, Andreas Charalambous, Haritini Tsangari, How do informal caregivers of patients with cancer cope: A descriptive study of the coping strategies employed, European Journal of Oncology Nursing, 2012, 16, 3, 258

    CrossRef

  41. 41
    Corinne Eleanor Fischer, Zahinoor Ismail, Tom A Schweizer, Impact of neuropsychiatric symptoms on caregiver burden in patients with Alzheimer’s disease, Neurodegenerative Disease Management, 2012, 2, 3, 269

    CrossRef

  42. 42
    Annakarin Olsson, Maria Engström, Kirsti Skovdahl, Claudia Lampic, My, your and our needs for safety and security: relatives’ reflections on using information and communication technology in dementia care, Scandinavian Journal of Caring Sciences, 2012, 26, 1
  43. 43
    Mi Ryeong Song, Young-Shin Lee, Jong-Duek Baek, Marci Miller, Physical Activity Status in Adults with Depression in the National Health and Nutrition Examination Survey, 2005–2006, Public Health Nursing, 2012, 29, 3
  44. 44
    Israel Contador, Bernardino Fernández-Calvo, David L. Palenzuela, Soraia Miguéis, Francisco Ramos, Prediction of burden in family caregivers of patients with dementia: A perspective of optimism based on generalized expectancies of control, Aging & Mental Health, 2012, 16, 6, 675

    CrossRef

  45. 45
    Heejung Kim, Mido Chang, Karen Rose, Sunha Kim, Predictors of caregiver burden in caregivers of individuals with dementia, Journal of Advanced Nursing, 2012, 68, 4
  46. 46
    Christine L. Carter, Eileen M. Resnick, Monica Mallampalli, Anna Kalbarczyk, Sex and Gender Differences in Alzheimer's Disease: Recommendations for Future Research, Journal of Women's Health, 2012, 21, 10, 1018

    CrossRef

  47. 47
    Evridiki Papastavrou, Andreas Charalambous, Haritini Tsangari, George Karayiannis, The Burdensome and Depressive Experience of Caring, Cancer Nursing, 2012, 35, 3, 187

    CrossRef

  48. 48
    June Lim, Jenny Goh, Hui Ling Chionh, Philip Yap, Why do patients and their families not use services for dementia? Perspectives from a developed Asian country, International Psychogeriatrics, 2012, 24, 10, 1571

    CrossRef

  49. 49
    Evridiki Papastavrou, Haritini Tsangari, George Karayiannis, Savvas Papacostas, Georgios Efstathiou, Panayiota Sourtzi, Caring and coping: The dementia caregivers, Aging & Mental Health, 2011, 15, 6, 702

    CrossRef

  50. 50
    Jennifer R. Day, Ruth A. Anderson, Compassion Fatigue: An Application of the Concept to Informal Caregivers of Family Members with Dementia, Nursing Research and Practice, 2011, 2011, 1

    CrossRef

  51. 51
    Rafael del-Pino-Casado, Antonio Frías-Osuna, Pedro A. Palomino-Moral, Pedro L. Pancorbo-Hidalgo, Coping and subjective burden in caregivers of older relatives: a quantitative systematic review, Journal of Advanced Nursing, 2011, 67, 11
  52. 52
    Rabia Khalaila, Howard Litwin, Does filial piety decrease depression among family caregivers?, Aging & Mental Health, 2011, 15, 6, 679

    CrossRef

  53. 53
    Burcu Akpınar, Özlem Küçükgüçlü, Görsev Yener, Effects of Gender on Burden Among Caregivers of Alzheimer's Patients, Journal of Nursing Scholarship, 2011, 43, 3
  54. 54
    Regina LT Lee, Esther SB Mok, Evaluation of the psychometric properties of a modified Chinese version of the Caregiver Task Inventory – refinement and psychometric testing of the Chinese Caregiver Task Inventory: a confirmatory factor analysis, Journal of Clinical Nursing, 2011, 20, 23-24
  55. 55
    Kevin M. Kieffer, George MacDonald, Exploring Factors That Affect Score Reliability and Variability, Journal of Individual Differences, 2011, 32, 1, 26

    CrossRef

  56. 56
    Graça Melo, João Maroco, Alexandre de Mendonça, Influence of personality on caregiver's burden, depression and distress related to the BPSD, International Journal of Geriatric Psychiatry, 2011, 26, 12
  57. 57
    Antonis A. Mougias, Antonis Politis, Constantine G. Lyketsos, Venetsanos G. Mavreas, Quality of life in dementia patients in Athens, Greece: predictive factors and the role of caregiver-related factors, International Psychogeriatrics, 2011, 23, 03, 395

    CrossRef

  58. 58
    Carmen de la Cuesta-Benjumea, Strategies for the relief of burden in advanced dementia care-giving, Journal of Advanced Nursing, 2011, 67, 8
  59. 59
    Ruth Landau, Gail K. Auslander, Shirli Werner, Noam Shoval, Jeremia Heinik, Who should make the decision on the use of GPS for people with dementia?, Aging & Mental Health, 2011, 15, 1, 78

    CrossRef

  60. 60
    R.D. Pattanayak, R. Jena, M. Tripathi, S.K. Khandelwal, Assessment of burden in caregivers of Alzheimer's disease from India, Asian Journal of Psychiatry, 2010, 3, 3, 112

    CrossRef

  61. 61
    Luis Agüera-Ortiz, Ana Frank-García, Pedro Gil, Alfonso Moreno, Clinical progression of moderate-to-severe Alzheimer's disease and caregiver burden: a 12-month multicenter prospective observational study, International Psychogeriatrics, 2010, 22, 08, 1265

    CrossRef

  62. 62
    T D Szucs, B Waeber, Y Tomonaga, Cost-effectiveness of antihypertensive treatment in patients 80 years of age or older in Switzerland: an analysis of the HYVET study from a Swiss perspective, Journal of Human Hypertension, 2010, 24, 2, 117

    CrossRef

  63. 63
    B. G. Knight, P. Sayegh, Cultural Values and Caregiving: The Updated Sociocultural Stress and Coping Model, The Journals of Gerontology Series B: Psychological Sciences and Social Sciences, 2010, 65B, 1, 5

    CrossRef

  64. 64
    M. Braun, U. Scholz, R. Hornung, M. Martin, Die subjektive Belastung pflegender Ehepartner von Demenzkranken, Zeitschrift für Gerontologie und Geriatrie, 2010, 43, 2, 111

    CrossRef

  65. 65
    Savvas Georgiades, Sensitive practice with Greek immigrants: a review of evidence, International Journal of Culture and Mental Health, 2010, 3, 1, 52

    CrossRef

  66. 66
    Evridiki Papastavrou, Andreas Charalambous, Haritini Tsangari, George Karayiannis, The cost of caring: the relative with schizophrenia, Scandinavian Journal of Caring Sciences, 2010, 24, 4
  67. 67
    V. MASKILL, M. CROWE, S. LUTY, P. JOYCE, Two sides of the same coin: caring for a person with bipolar disorder, Journal of Psychiatric and Mental Health Nursing, 2010, 17, 6
  68. 68
    Ruth Landau, Shirli Werner, Gail K. Auslander, Noam Shoval, Jeremia Heinik, What do cognitively intact older people think about the use of electronic tracking devices for people with dementia? A preliminary analysis, International Psychogeriatrics, 2010, 22, 08, 1301

    CrossRef

  69. 69
    Katherine C. Hutchinson, Victoria W. Willard, Kristina K. Hardy, Melanie J. Bonner, Adjustment of caregivers of pediatric patients with brain tumors: a cross-sectional analysis, Psycho-Oncology, 2009, 18, 5
  70. 70
    Susan Bookheimer, Alison Burggren, APOE-4 Genotype and Neurophysiological Vulnerability to Alzheimer's and Cognitive Aging, Annual Review of Clinical Psychology, 2009, 5, 1, 343

    CrossRef

  71. 71
    R. Landau, S. Werner, G. K. Auslander, N. Shoval, J. Heinik, Attitudes of Family and Professional Care-Givers towards the Use of GPS for Tracking Patients with Dementia: An Exploratory Study, British Journal of Social Work, 2009, 39, 4, 670

    CrossRef

  72. 72
    Evridiki Papastavrou, Andreas Charalambous, Haritini Tsangari, Exploring the other side of cancer care: The informal caregiver, European Journal of Oncology Nursing, 2009, 13, 2, 128

    CrossRef

  73. 73
    Andrea Bradford, Mark E. Kunik, Paul Schulz, Susan P. Williams, Hardeep Singh, Missed and Delayed Diagnosis of Dementia in Primary Care, Alzheimer Disease & Associated Disorders, 2009, 23, 4, 306

    CrossRef

  74. 74
    Carla J. M. Schölzel-Dorenbos, Irena Draskovic, Myrra J. Vernooij-Dassen, Marcel G. M. Olde Rikkert, Quality of Life and Burden of Spouses of Alzheimer Disease Patients, Alzheimer Disease & Associated Disorders, 2009, 23, 2, 171

    CrossRef

  75. 75
    Johan Lökk, Reduced life-space of non-professional caregivers to Parkinson's disease patients with increased disease duration, Clinical Neurology and Neurosurgery, 2009, 111, 7, 583

    CrossRef

  76. 76
    Kevin L. Baker, Noelle Robertson, Coping with caring for someone with dementia: Reviewing the literature about men, Aging & Mental Health, 2008, 12, 4, 413

    CrossRef

  77. 77
    P. Campbell, J. Wright, J. Oyebode, D. Job, P. Crome, P. Bentham, L. Jones, C. Lendon, Determinants of burden in those who care for someone with dementia, International Journal of Geriatric Psychiatry, 2008, 23, 10
  78. 78
    Jennifer Merrilees, A Model for Management of Behavioral Symptoms in Frontotemporal Lobar Degeneration, Alzheimer Disease & Associated Disorders, 2007, 21, 4, S64

    CrossRef