Influence of Sense of Competence, Empathy and Relationship Quality on Burden in Dementia Caregivers: A 15 Months Longitudinal Study

被引:3
|
作者
van den Kieboom, Robin [1 ,2 ,6 ]
Mark, Ruth [3 ]
Snaphaan, Liselore [1 ,2 ]
van Assen, Marcel [4 ,5 ]
Bongers, Inge [1 ,2 ]
机构
[1] Tilburg Univ, Tilburg Sch Social & Behav Sci, Tranzo, Tilburg, Netherlands
[2] Mental Hlth Care Inst Eindhoven, Res Unit Evidence Based Management Innovat, Eindhoven, Netherlands
[3] Tilburg Univ, Tilburg Sch Social & Behav Sci, Dept Cognit Neuropsychol, Tilburg, Netherlands
[4] Tilburg Univ, Tilburg Sch Social & Behav Sci, Dept Methodol & Stat, Tilburg, Netherlands
[5] Univ Utrecht, Dept Sociol, Utrecht, Netherlands
[6] Tilburg Univ, Tilburg Sch Social & Behav Sci, Cobbenhagenlaan 125, NL-5037 DB Tilburg, Noord Brabant, Netherlands
关键词
dementia; caregiving; longitudinal methods; ALZHEIMERS-DISEASE; MULTIPLE IMPUTATION; SATISFACTION; PROGRESSION; DEPRESSION; PATIENT; MODELS; HEALTH; CRA;
D O I
10.1177/07334648221138545
中图分类号
R4 [临床医学]; R592 [老年病学];
学科分类号
1002 ; 100203 ; 100602 ;
摘要
Objectives: The aim is to explore the trajectory of caregiver burden and how this relates to caregiver and contextual factors in community-dwelling dyads. Methods: At baseline, 201 family caregivers were included. The multidimensional construct of family caregiver burden and the effects of sense of competence, empathy, and quality of the relationship on this burden were assessed over 15 months using semi-structured interviews and questionnaires. Results: We found an increase of burden linked to disruptions in the caregiver's own usual activities (p = 0.002) and physical health complaints (p = 0.001). Caregivers with a high sense of competence experienced lower caregiver burden during the entire caregiving process (p < 0.001). Discussion: Healthcare professionals should alert family caregivers to the importance of taking care of themselves as early as possible in their new caregiver role. Caregiving is demanding and could negatively influence their own activities and physical health.
引用
收藏
页码:464 / 473
页数:10
相关论文
共 50 条
  • [31] Dealing with Daily Challenges in Dementia (Deal-id Study): An Experience Sampling Study to Assess Caregivers' Sense of Competence and Experienced Positive Affect in Daily Life
    van Knippenberg, Rosalia J. M.
    de Vugt, Marjolein E.
    Ponds, Rudolf W.
    Myin-Germeys, Inez
    Verhey, Frans R. J.
    AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY, 2017, 25 (08): : 852 - 859
  • [32] Relationship quality in dementia: Preliminary longitudinal analyses of the EU-JPND Actifcare cohort study
    Marques, Maria J.
    Woods, Bob
    Tan, Eva Y. L.
    de Vugt, Marjolein
    Verhey, Frans
    Goncalves-Pereira, Manuel
    INTERNATIONAL PSYCHOGERIATRICS, 2020, 32 : 83 - 83
  • [33] The relationship between psychological burden and providing assistance with taking medication among caregivers of patients with dementia: a cross-sectional study
    Fuga, Habuchi
    Yamaoka, Erika
    Ishida, Natsuko
    Shitanda, Koji
    Hashimoto, Masako
    Matushita, Ryo
    INTERNATIONAL JOURNAL OF PHARMACY PRACTICE, 2024, 32 (05) : 377 - 383
  • [34] A Multicomponent Home-Based Intervention for Neuropsychiatric Symptoms in People With Dementia and Caregivers' Burden and Depression: A 6-Month Longitudinal Study
    Mougias, Antonis A.
    Christidi, Foteini
    Kontaxopoulou, Dionysia
    Zervou, Mariyanna
    Kostoglou, Dimitra
    Vlami, Maria Anna
    Dimitriou, Maria
    Politis, Antonis
    JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY, 2022, 35 (04) : 535 - 543
  • [35] Caregiver burden, psychological distress and quality of life among informal caregivers of patients with head and neck cancer: a longitudinal study
    van Hof, Kira
    Hoesseini, Arta
    Dorr, Maarten
    Verdonck-de Leeuw, Irma
    Jansen, Femke
    Leemans, Renee
    Smit, Jan
    Takes, Robert
    Terhaard, Chris
    de Jong, Robert Jan Baatenburg
    Sewnaik, Aniel
    Offerman, Marinella
    QUALITY OF LIFE RESEARCH, 2022, 31 : S76 - S77
  • [36] Caregiver Burden, Psychological Distress and Quality of Life among Informal Caregivers of Patients with Head and Neck Cancer: A Longitudinal Study
    Van Hof, Kira S. S.
    Hoesseini, Arta
    Dorr, Maarten C. C.
    Verdonck-de Leeuw, Irma M. M.
    Jansen, Femke
    Leemans, C. Rene
    Takes, Robert P. P.
    Terhaard, Chris H. J.
    Baatenburg de Jong, Robert Jan
    Sewnaik, Aniel
    Offerman, Marinella P. J.
    INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, 2022, 19 (23)
  • [37] Caring burden and quality of life among the caregivers of people living with dementia - a cross-sectional study in Udupi district of Karnataka
    Martis, Clarita Shynal
    Bhandary, Rajeshkrishna Panambur
    Chandrababu, Ramesh
    Lakshmi, Vani R.
    Bhandary, Panambur Venkataraya
    Noronha, Judith Angelitta
    Chakrabarty, Jyothi
    Tolson, Debbie
    Devi, Elsa Sanatombi
    HOME HEALTH CARE SERVICES QUARTERLY, 2024, 43 (03) : 191 - 204
  • [38] Changes in caregiving appraisal among family caregivers of persons with dementia: A longitudinal study over 12 months (vol 18, pg 460, 2018)
    Kajiwara, K.
    Noto, H.
    Yamanaka, M.
    PSYCHOGERIATRICS, 2019, 19 (05) : 523 - 523
  • [39] The relationship between daily stressors, social support, depression and anxiety among dementia family caregivers: a micro-longitudinal study
    Puga, Frank
    Wang, Danny
    Rafford, Meghan
    Poe, Abigail
    Pickering, Carolyn E. Z.
    AGING & MENTAL HEALTH, 2023, 27 (07) : 1291 - 1299
  • [40] A Preliminary Study of Anticholinergic Burden and Relationship to a Quality of Life Indicator, Engagement in Activities, in Nursing Home Residents With Dementia
    Kolanowski, Ann
    Fick, Donna M.
    Campbell, Judy
    Litaker, Mark
    Boustani, Malaz
    JOURNAL OF THE AMERICAN MEDICAL DIRECTORS ASSOCIATION, 2009, 10 (04) : 252 - 257