The Moderating Influence of Service use on Negative Caregiving Consequences

Bass, D. M., Noelker, L. S., Rechlin, L. R.·1996·The Journals of Gerontology Series B: Psychological Sciences and Social Sciences

Cited by (158)

Items 101–158 of 158

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  7. FAMILY CAREGIVING AND THE USE OF FORMAL COMMUNITY SUPPORT SERVICES: A QUALITATIVE CASE STUDY
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  8. An Integrated Program for Dementia Evaluation and Care Management
    Nancy L. Morrow-Howell, D. M. Freed, W.W. Elder, Sean A. Lauderdale, S. Carter · 1999 · The Gerontologist
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  10. Utilization of home-based care and its buffering effects between dementia caregiving intensity and caregiver burden in China
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  11. Insight Into Dementia Care Management Using Social-Behavioral Theory and Mixed Methods
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  13. Depression among caregivers of the elderly in need of care and their service utilization: A pilot study
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  15. Predictors of acceptance of offered care management intervention services in a quality improvement trial for dementia
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  16. Frequency, Duration, and Social Context of Activities in Daily Living: Time‐budget Methodology for Caregiving Research
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  17. Unmet Needs for Supportive Services
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  18. Building an advocacy model to improve the dementia‐capability of health plans in California
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  20. Burdened but Meaningful?: How Gender Role Attitudes Influence the Complex Links between Care-giver Self-Efficacy, Formal Support Utilisation and Benefit-Finding among Spousal Care-givers
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  21. Predictors of perceived benefits and drawbacks of using paid service among daughter and daughter-in-law caregivers of people with dementia
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  22. Support for Family Caregivers: Implications of Work Strain and Its Intersections With Formal and Informal Help
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  23. The Impace of Health Care Provider Communication on Self-Efficacy and Caregiver Burden in Older Spousal Oncology Caregivers
    Joyce J Grater · 2005 · D-Scholarship@Pitt (University of Pittsburgh)
  24. Caregivers of Children Infected and/or Affected by HIV/AIDS
    Scott D. Ryan · 2001 · OhioLink ETD Center (Ohio Library and Information Network)
  25. Dementia Cal MediConnect: Creating Partnerships Between Health Plans and Alzheimer’s Organizations to Improve Care in the Dual Eligibles Pilot
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  26. How Concurrent Services Obscured Detection of Intervention Benefits: Part 2: Secondary Analysis of the PREP Trial for Frail Older Adults and Family Caregivers
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  28. How Do Shifts in Patients with Mental Health Problems’ Formal and Informal Care Utilization Affect Informal Caregivers?: A COVID-19 Case Study
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  31. Repercusión de la enfermedad de Alzheimer en el núcleo familiar
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  32. Targeting Interventions for Primary Informal Caregivers of Adults with Cognitive and Physical Losses
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  33. Social support
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  34. Evaluating the Efficacy and Acceptability of the Empowered Caregiver Program on Caregivers of People Living with Dementia
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  35. Advances in Alzheimer’s Disease Research: Implications for Family Caregiving
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  38. Commentary by Capitman
    John A. Capitman · 2005 · Journal of Aging and Health
  39. Understanding friends and family members' experiences of going abroad with medical tourists
    Victoria Casey · 2013 · Summit (Simon Fraser University)
  40. Psychological Co-morbidities of Dementia
    Carla Bejjani, Mark E. Kunik · 2011 · Springer eBooks
  41. Impact of Care-Recipient Resistance During Care Provision on Caregiver Emotional/Physical Well-Being: A Sequential Mixed Method Design with Between- and Within-Person Analyses and Semi-Structured Interviews
    Yumi Shirai · 2011 · UA Campus Repository (The University of Arizona)
  42. Communities in profile: A comparison of caregiving in Glace Bay and Kings County
    Deborah Kiceniuk, A. Fiona MacKenzie, Andrew Harvey · 2003 · DalSpace (Dalhousie University)
  43. "It reminds me that I'm still me": Social programs for younger persons with dementia
    Sarah H. Main · 2016 · UWSpace (University of Waterloo)
  44. How the Illness Experience Predicts Key Psychosocial Outcomes in Veterans with Brain Injury
    Carmen M. Tyler · 2017 · EngagedScholarship @ Cleveland State University (Cleveland State University)
  45. Increases in informal caregiver psychological distress and physical health symptoms lead to poor quality of care over time
    G. Rush Smith · 2010
  46. Effektivität psychosozialer und psychotherapeutischer Interventionsansätze für pflegende Angehörige von Menschen mit Demenz
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  48. Prendre soin d'un proche âgé
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  49. Formal long-term care : informal caregivers’ subjective well-being and service utilization
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  50. International Journal of Business and Management, Vol. 3, No. 8, August 2008
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  53. Different patterns among caregivers in their utilization of formal services and the influence on caregiver burden and health
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  54. Additional file 1 of Supporting caregivers of veterans with Alzheimer’s disease and traumatic brain injury: study protocol for a randomized controlled trial
    Jennifer L. Carnahan, Katherine S. Judge, Joanne Daggy, James E. Slaven, Nicki Coleman, Emily L. Fortier, Christopher Suelzer, Nicole R. Fowler · 2020 · Figshare
  55. Validity testing of the Benjamin Rose Unmet Need Instrument: a comprehensive measure for dementia caregiving
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