In response to inquiries from AGE-WELL members and affiliates about the needs of caregivers, a repository was constructed to house article references and abstracts produced and/or used by WP2 members between 2000-2020.
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Eisdorfer, C., Czaja, S. J., Loewenstein, D. A., Rubert, P. M , Arguelles, S., Mitrani, V. B., & Szapocznik, J. (2003). The effect of a family therapy and technology-based intervention on caregiver depression. Gerontologist, 43(4), 521–531. https://www.ncbi.nlm.nih.gov/pubmed/12937331
Fast, J., Williamson, D. L., & Keating, N. (1999). The hidden costs of informal elder care. Journal of Family and Economic Issues, 20(3), 301–326. https://doi.org/10.1023/A:1022909510229
Silva, A. L., Teixeira, H. J., Teixeira, J. M , & Freitas, S. (2013). The needs of informal caregivers of elderly people living at home: an integrative review. Scand J Caring Sci, 27(4), 792–803. https://doi.org/10.1111/scs.12019
Yon, Y., Wister, A. V., Mitchell, B., & Gutman, G. (2014). A national comparison of spousal abuse in mid- and old age. J Elder Abuse Negl, 26(1), 80–105. https://doi.org/10.1080/08946566.2013.784085
Noreau, L., Edwards, E., Boucher, N., 2191, Vincent, C., Gascon, H., & Fougeyrollas, P. (2015). Enhancing Independent Community Access and Participation: Services, Technologies and Policies. . Oxford University Press.
Kinnane, N. A., & Milne, D. J. (2010). The role of the Internet in supporting and informing carers of people with cancer: a literature review. Support Care Cancer, 18(9), 1123–1136. https://doi.org/10.1007/s00520-010-0863-4
Mehta, R., & Dwan, N. (2016). Atlas of Caregiving Pilot: Study Report. . https://atlasofcaregiving.com/wp-content/uploads/2016/03/Study_Report.pdf
Clyne, B., Pierscionek, B., Gonzaga-Chorro, C.-., Comiskey, C., Monekosso, D. N., Heery, D., Florez, F., Fortune, H., Doyle, J., Dinsmore, J., Lecumberr-Ciaurriz, J.-., Lazaro-Ramos, J.-., Cullen, K., Arego-Fernandez, M., Chambers, M., Harris, N., Delaney, S., & Kantaris, X. (2014). White Paper On Needs And Requirements Of Aal And Ict Solutions For Informal Long-Term Care Of Elderly People. http://www.breathe-project.eu/gallery/17/White_paper_on_needs_and_requirements_of_AAL_and_ICT_solutions_of_informal_LTC_of_elderly_people.pdf
Keating, N., Fast, J., Lero, D., Lucas, S., & Eales, J. (2014). A taxonomy of the economic costs of family care to adults. Journal of the Economics of Aging, 3, 11–20. http://www.sciencedirect.com/science/article/pii/S2212828X1400005X
Fast, J., Keating, N., Otfinowski, P., & Derksen, L. (2004). Characteristics of Family/Friend Care Networks of Frail Seniors. Canadian Journal on Aging / La Revue Canadienne Du Vieillissement, 23(1), 5–19. https://www.ncbi.nlm.nih.gov/pubmed/15310087
Huber, L. L., Shankar, K., Caine, K., Connelly, K., Camp, L. J., Walker, B. A., & Borrero, L. (2013). How In-Home Technologies Mediate Caregiving Relationships in Later Life. International Journal of Human–Computer Interaction, 29(7), 441–455. https://doi.org/10.1080/10447318.2012.715990
Fast, J., Eales, J., & Keating, N. (2008). Final commentary for CJA supplemental issue: the hidden costs of care. Can J Aging, 27(1), 3–5. https://doi.org/10.3138/cja.27.1.003
Powers, S. M., & Whitlatch, C. J. (2016). Measuring cultural justifications for caregiving in African American and White caregivers. Dementia (London), 15(4), 629–645. https://doi.org/10.1177/1471301214532112
Leslie, M., Eales, J., Fast, J., Mortenson, B., Atoyebi, O., & Mahani, A. (2018). From ‘Needs’ to ‘Goals’: Evolving the User Centered Design process for technology supporting family caregivers. Assistive Technology.
Motiwala, S. S., Flood, C. M., Coyte, P. C., & Laporte, A. (2005). The First Ministers’ Accord on Health Renewal and the Future of Home Care in Canada. Longwoods Review, 2(4), 1–10.
Duxbury, L., Higgins, C., & Schroeder, B. (2009). Balancing paid work and caregiving responsibilities: A closer look at family caregivers in Canada. http://www.cprn.org/documents/51061_EN.pdf
Bank, A. L., Arguelles, S., Rubert, M., Eisdorfer, C., & Czaja, S. J. (2006). The value of telephone support groups among ethnically diverse caregivers of persons with dementia. Gerontologist, 46(1), 134–138. https://www.ncbi.nlm.nih.gov/pubmed/16452294
Lashewicz, B., Manning, G., Hall, M., & Keating, N. (2007). Equity matters: doing fairness in the context of family caregiving. Can J Aging, 26 Suppl 1, 91–102. https://doi.org/10.3138/cja.26.suppl_1.091
Kristjanson, L. J., & Aoun, S. (2004). Palliative care for families: remembering the hidden patients. Can J Psychiatry, 49(6), 359–365. https://doi.org/10.1177/070674370404900604
Wang, J., Carroll, D., Peck, M., Myneni, S., & Gong, Y. (2016). Mobile and Wearable Technology Needs for Aging in Place: Perspectives from Older Adults and Their Caregivers and Providers. Stud Health Technol Inform, 225, 486–490.
Chiu, T. M., & Eysenbach, G. (2011). Theorizing the health service usage behavior of family caregivers: a qualitative study of an internet-based intervention. Int J Med Inform, 80(11), 754–764. https://doi.org/10.1016/j.ijmedinf.2011.08.010
Demers, L., Fuhrer, J. M , Jutai, J., Lenker, J., Depa, M., & Ruyter, F. D. (2009). A conceptual framework of outcomes for caregivers of assistive technology users. Am J Phys Med Rehabil, 88(8), 645–655; quiz 656–658, 691. https://doi.org/10.1097/PHM.0b013e3181ae0e70
Deeken, J. F., Taylor, K. L., Mangan, P., Yabroff, K. R., & Ingham, J. M. (2003). Care for the caregivers: a review of self-report instruments developed to measure the burden, needs, and quality of life of informal caregivers. J Pain Symptom Manage, 26(4), 922–953. https://www.ncbi.nlm.nih.gov/pubmed/14527761
Keating, N., Otfinowski, P., Wenger, C., Fast, J., & Derksen, L. (2003). Understanding the caring capacity of informal networks of frail seniors: A case for care networks. Ageing and Society, 23(1), 115–127. https://doi.org/10.1017/S0144686X02008954
Montague, T., Gogovor, A., Ahmed, S., Torr, E., Aylen, J., Marshall, L., Henningsen, N., & Nemis-White, J. (2015). Contributions and Challenges of Non-Professional Patient Care: A Key Component of Contemporary Canadian Healthcare. Healthc Q, 18(3), 18–22. https://www.ncbi.nlm.nih.gov/pubmed/26718249
Rabow, W. M , Hauser, J. M., & Adams, J. (2004). Supporting family caregivers at the end of life: "they don’t know what they don’t know. JAMA, 291(4), 483–491. https://doi.org/10.1001/jama.291.4.483
McCabe, M., You, E., & Tatangelo, G. (2016). Hearing Their Voice: A Systematic Review of Dementia Family Caregivers’ Needs. Gerontologist, 56(5), e70-88. https://doi.org/10.1093/geront/gnw078
Fast, J., Dosman, D., Lero, D., & Lucas, S. (2013). The Intersection of Caregiving and Employment Across the Life Course. http://rapp.ualberta.ca/Portals/116/Documents/Reports/IntersectionCaregivingAndEmployment2013Jan.pdf?ver=2016-06-15-144900-460
team, C. P., & House, W. (2010). Recognised, valued and supported: next steps for the Carers Strategy. https://www.gov.uk/government/uploads/system/uploads/attachment_data/file/213804/dh_122393.pdf
Mortenson, W. B. (2014, November). Development and preliminary evaluation of the caregiver assistive technology outcome measure. Gerontology Society of America.
Beaudoin, M., Atoyebi, O., Mortenson, B., Auger, C., Demers, L., Wister, A., Plante, M., & Routhier, F. (2019). Interviews with family caregivers of older adults: Their experiences of care and the integration of assistive technology in care. Technology and Disability.
Fast, J., Keating, N., Eales, J., Kim, C., & Lee, Y. (2019). Trajectories of family care over the life course: evidence from Canada. Ageing and Society.
Luchesi, B. M., Souza, E. N., Gratao, A. C., Gomes, G. A., Inouye, K., Tda, S. A., Marques, S., & Pavarini, S. C. (2016). The evaluation of perceived stress and associated factors in elderly caregivers. Arch Gerontol Geriatr, 67, 7–13. https://doi.org/10.1016/j.archger.2016.06.017
Schulz, R., O’Brien, A. T., Bookwala, J., & Fleissner, K. (1995). Psychiatric and physical morbidity effects of dementia caregiving: prevalence, correlates, and causes. Gerontologist, 35(6), 771–791. https://www.ncbi.nlm.nih.gov/pubmed/8557205
American, [ A. (2016). Caregiver and technology: What they want and need. https://www.aarp.org/content/dam/aarp/research/surveys_statistics/ltc/2018/caregivers-technology-needs.doi.10.26419-2Fres.00191.002.pdf
Labbé, D., Mortenson, B., Rushton, P., Demers, L., & Miller, B. (2018). Longitudinal Outcomes Among Family Caregiver’s of Power Mobility Users. Archives of Physical Medicine and Rehabilitation. https://doi.org/https://doi.org/10.1016/j.apmr.2018.08.194
Keating, N., Eales, J., Funk, L., Fast, J., & Min, J. (2019). Life course trajectories of family care. International Journal of Care and Caring. https://doi.org/https://doi.org/10.1332/239788219X15473079319309
Mihailidis, A., Cockburn, A., Longley, C., & Boger, J. (2008). The acceptability of home monitoring technology among community-dwelling older adults and baby boomers. Assistive Technology, 20(1), 1–12. https://doi.org/10.1080/10400435.2008.10131927
Boger, J., Quraishi, M., Turcotte, N., & Dunal, L. (2014). The identification of assistive technologies being used to support the daily occupations of community-dwelling older adults with dementia: a cross-sectional pilot study. Disabil Rehabil Assist Technol, 9. https://doi.org/10.3109/17483107.2013.785035
Study, C. H. C. H. R. C. (2003). Synthesis Report. The Home Care Sector Study Corporation. http://tools.hhr-rhs.ca/index.php?option=com_mtree&task=viewlink&link_id=5228&Itemid=109&lang=en
Donelan, K., Hill, C. A., Hoffman, C., Scoles, K., Feldman, P. H., Levine, C., & Gould, D. (2002). Challenged to care: informal caregivers in a changing health system. Health Aff (Millwood), 21(4), 222–231. https://www.ncbi.nlm.nih.gov/pubmed/12117133
Chapman, S. A., Keating, N., & Eales, J. (2003). Client-centred, community-based care for frail seniors. Health Soc Care Community, 11(3), 253–261. https://www.ncbi.nlm.nih.gov/pubmed/12823430
Cranswick, K., & Dosman, D. (2007). Eldercare:What we know today. http://www.statcan.gc.ca/pub/11-008-x/2008002/article/10689-eng.htm#footnote2
Kenny, P. M., Hall, J. P., Zapart, S., & Davis, P. R. (2010). Informal care and home-based palliative care: the health-related quality of life of carers. J Pain Symptom Manage, 40(1), 35–48. https://doi.org/10.1016/j.jpainsymman.2009.11.322
Labbé, D., Miller, B., Rushton, P., Routhier, F., Demers, L., & Mortenson, B. (2019). Positive experiences and resources of caregivers of powered wheelchair users: a qualitative inquiry. Disability and Rehabilitation.
Kirby, R. L., Rushton, P., Routhier, F., Demers, L., Titus, L., Miller-Polgar, J., Smith, C., McAllister, M., Theriault, C., Matheson, K., Parker, K., Sawatzky, B., Labbe, D., & Miller, B. (2018). The extent to which caregivers enhance the wheelchair skills capacity and confidence of power wheelchair users: a cross-sectional study. Archives of Physical Medicine and Rehabilitation, S0003-9993(17), 31462–31464. https://doi.org/10.1016/j.apmr.2017.11.014
Leslie, M., Eales, J., Fast, J., Mortenson, B., Atoyebi, O., & Mahani, A. (2019). Towards sustainable family care: Using goals to re-frame the user-centred design of technologies to support carers. International Journal of Care and Caring, 1–7. https://doi.org/https://doi.org/10.1332/239788219X15597493546652
Keating, N., Swindle, J., & Fletcher, S. (2011). Aging in rural Canada: a retrospective and review. Can J Aging, 30(3), 323–338. https://doi.org/10.1017/s0714980811000250
Pysklywec, A., Plante, M., Auger, C., Mortenson, B., Eales, J., Routhier, F., & Demers, L. (2019). The positive effects of caregiving for family caregivers of older adults: A scoping review. International Journal of Care and Caring.
Keating, N., & Eales, J. (2017). Social consequences of family care of adults: a scoping review. International Journal of Care and Caring, 1(2), 153–173. https://doi.org/10.1332/239788217X14937990731749
for N. Caregiving, N. A., & Care, U. H. U. (2011). e‑Connected Family Caregiver: Bringing Caregiving into the 21st Century. www.caregiving.org/data/FINAL_eConnected_Family_Caregiver_Study_Jan 2011.pdf
Black, B. S., Johnston, D., Rabins, P. V., Morrison, A., Lyketsos, C., & Samus, Q. M. (2013). Unmet needs of community-residing persons with dementia and their informal caregivers: findings from the maximizing independence at home study. J Am Geriatr Soc, 61(12), 2087–2095. https://www.ncbi.nlm.nih.gov/pubmed/24479141
Mahoney, D. F. (2010). An Evidence-Based Adoption of Technology Model for Remote Monitoring of Elders’ Daily Activities. Ageing Int, 36(1), 66–81. https://doi.org/10.1007/s12126-010-9073-0
Farley, N., Demers, L., & Swaine, B. R. (2008). Development of the French Canadian version of the Montgomery Borgatta caregiver burden scale]. Can J Aging, 27(2), 181–190. https://doi.org/10.3138/cja.27.2.181
Lero, D., Keating, N., Fast, J., Joseph, & Cook, A. (2007). The Interplay of Risk Factors Associated with Negative Outcomes among Family Caregivers: A Synthesis of the Literature. http://www.worklifecanada.ca/cms/resources/files/718/The_interplay_of_risk_factors_associated_with_negative_outcomes_among_family_caregivers_2007.pdf
McMillan, S. C. (2005). Interventions to facilitate family caregiving at the end of life. J Palliat Med, 8 Suppl 1, S132-9. https://doi.org/10.1089/jpm.2005.8.s-132
Beaudoin, M., Atoyebi, O., Mortenson, B., Auger, C., Demers, L., Wister, A., Plante, M., & Routhier, F. (2019). Être le proche aidant d’une personne âgée vivant avec des incapacités : Résultats préliminaires d’une étude qualitative. PluriÂges.
Mortenson, W. B., Demers, L., Fuhrer, J. M , Jutai, J. W., Lenker, J., & DeRuyter, F. (2012). How assistive technology use by individuals with disabilities impacts their caregivers: a systematic review of the research evidence. Am J Phys Med Rehabil, 91(11), 984–998. https://doi.org/10.1097/PHM.0b013e318269eceb
Edwards, B. (2008). The nature and impact of caring for family members with a disability in Australia. https://aifs.gov.au/publications/nature-and-impact-caring-family-members-di/executive-summary
Strickfaden, M. (2018). Caring by Design: Innovating Living Spaces for Persons with Dementia. Design Community Journal Special Issue on Rehabilitation and Aging Environments in Western Canada, 4(86), 46–71.
Rochette, A., Racine, E., Lefebvre, H., Lacombe, J., Bastien, J., & Tellier, M. (2014). Ethical issues relating to the inclusion of relatives as clients in the post-stroke rehabilitation process as perceived by patients, relatives and health professionals. Patient Educ Couns, 94(3), 384–389. https://doi.org/10.1016/j.pec.2013.10.028
Hollander, J. M , Liu, G., & Chappell, N. L. (2009). Who cares and how much? The imputed economic contribution to the Canadian healthcare system of middle-aged and older unpaid caregivers providing care to the elderly. Healthc Q, 12(2), 42–49.
Liu, L., Stroulia, E., Nikolaidis, I., Miguel-Cruz, A., & Rios-Rincon, A. (2016). Smart homes and home health monitoring technologies for older adults: A systematic review. International Journal of Medical Informatics. https://doi.org/http://dx.doi.org/10.1016/j.ijmedinf.2016.04.007
Schulz, R., & Martire, L. M. (2009). Caregiving and employment. The Johns Hopkins University Press.
Hammel, J., Southall, K., Jutai, J., Finlayson, M., Kashindi, G., & Fok, D. (2013). Evaluating use and outcomes of mobility technology: a multiple stakeholder analysis. Disability and Rehabilitation: Assistive Technology, 8(4), 294–304. https://doi.org/10.3109/17483107.2012.735745
Mortenson, B., Pysklywec, A., Fuhrer, M. J., Jutai, J., Plante, M., & Demers, L. (2018). Caregivers’ experiences with the selection and use of assistive technology. Disability and Rehabilitation: Assistive Technology, 13(6), 562–567. https://doi.org/10.1080/17483107.2017.1353652
Greenwood, N., Mackenzie, A., Cloud, G. C., & Wilson, N. (2008). Informal carers of stroke survivors–factors influencing carers: a systematic review of quantitative studies. Disabil Rehabil, 30(18), 1329–1349. https://www.ncbi.nlm.nih.gov/pubmed/19230230
team, T. N. (2010). Survey of Carers in Households 2009/10. http://content.digital.nhs.uk/catalogue/PUB02200/surv-care-hous-eng-2009-2010-rep1.pdf
Schwarz, K. A., & Dunphy, G. (2003). An examination of perceived stress in family caregivers of older adults with heart failure. Exp Aging Res, 29(2), 221–235. https://doi.org/10.1080/03610730303717
McIlfatrick, S. (2007). Assessing palliative care needs: views of patients, informal carers and healthcare professionals. J Adv Nurs, 57(1), 77–86. https://doi.org/10.1111/j.1365-2648.2006.04062.x
Sawatzky, J. E., & Fowler-Kerry, S. (2003). Impact of caregiving: listening to the voice of informal caregivers. J Psychiatr Ment Health Nurs, 10(3), 277–286. https://www.ncbi.nlm.nih.gov/pubmed/12755912
Hudson, P. L., Remedios, C., & Thomas, K. (2010). A systematic review of psychosocial interventions for family carers of palliative care patients. BMC Palliat Care, 9, 17. https://doi.org/10.1186/1472-684X-9-17
Hoff, A. (2009). Families, care and work: changes and challenges. http://www.oxfordmartin.ox.ac.uk/publications/view/74
Keating, N., & Dosman, D. (2009). Social capital and the care networks of frail seniors. Can Rev Sociol, 46(4), 301–318. https://www.ncbi.nlm.nih.gov/pubmed/20481408
Gélinas-Bronsard, D., Mortenson, B., Ahmed, S., Guay, C., & Auger, C. (2018). undefinedCo-construction of an Internet-based Intervention for Older Assistive Technology Users and their Family Caregivers: Stakeholders’ Perceptions". Disability and Rehabilitation: Assistive Technology. .
Hamann, J., Charette, C., Best, K., Smith, E. M., Miller, B., & Routhier, F. (2018). La marche du temps . Le Fil , 54(6). https://www.lefil.ulaval.ca/la-marche-du-temps/
Goodhead, A., & McDonald, J. (2007). Informal caregivers literature review. http://www.moh.govt.nz/notebook/nbbooks.nsf/0/fb327285c9043995cc25734500069193/FILE/informal-caregivers-literature-review.pdf
Keating, N., & d. Gierveld, J. (2015). Editorial: Families and Aging: From Private Troubles to a Global Agenda. Can J Aging, 34(3), 261–263. https://doi.org/10.1017/s0714980815000276
Hastall, M., Eiermann, N., & Ritterfeld, U. (2014). Formal and informal carers’ views on ICT in dementia care: Insights from two qualitative studies. Gerontechnology, 13(1), 51–56. https://doi.org/10.4017/gt.2014.13.1.003.00
Ahmed, S., Gogovor, A., Kosseim, M., Poissant, L., Riopelle, R., Simmonds, M., Krelenbaum, M., & Montague, T. (2010). Advancing the chronic care road map: a contemporary overview. Healthc Q, 13(3), 72–79.
Bien-Barkowska, K., Doroszkiewicz, H., & Bien, B. (2017). Silent strain of caregiving: exploring the best predictors of distress in family carers of geriatric patients. Clinical Interventions in Aging, 2017(12), 263–274. https://doi.org/https://doi.org/10.2147/CIA.S125664
Lero, D., & Fast, J. (2018). The availability and use of flexible work arrangements and caregiving leaves: Lessons learned about policies and practice. Journal of Law and Equity.
Duggleby, W., Robinson, C. A., Kaasalainen, S., Pesut, B., Nekolaichuk, C., MacLeod, R., Keating, N. C., Salas, A. S., Hallstrom, L. K., Fraser, K. D., Williams, A., Struthers-Montford, K., & Swindle, J. (2016). Developing Navigation Competencies to Care for Older Rural Adults with Advanced Illness. Can J Aging, 35(2), 206–214. https://doi.org/10.1017/s0714980816000131
Juleen, R., Rocco, R. P. B. P., Maqui, O., Barbara, F., Richard, S., Morton, M. S. C. S., Caine, L. S., Lu, H., & Everette, J. A. (2017). Caregiver Integration During Discharge Planning for Older Adults to Reduce Resource Use: A Metaanalysis. Journal of the American Geriatrics Society, 65(8), 1748–1755. https://doi.org/doi:10.1111/jgs.14873
Washington, K. T., Meadows, S. E., Elliott, S. G., & Koopman, R. J. (2011). Information needs of informal caregivers of older adults with chronic health conditions. Patient Educ Couns, 83(1), 37–44. https://doi.org/10.1016/j.pec.2010.04.017
Auger, C. (2007). Applicability of a toolkit for geriatric rehabilitation outcomes. Disability and Rehabilitation, 29(2), 97–109.
Gélinas-Bronsard, D., Mortenson, B., Ahmed, S., Guay, M., & Auger, C. (2018). Co-construction of an Internet-based intervention for older assistive technology users and their family caregivers: Needs identification phase. Disability and Rehabilitation.
Stajduhar, K., Funk, L., Toye, C., Grande, G., Aoun, S., & Todd, C. (2010). Part 1: Home-based family caregiving at the end of life: a comprehensive review of published quantitative research (1998-2008). Palliat Med, 24(6), 573–593. https://doi.org/10.1177/0269216310371412
Mortenson, W. B. (2013). Effects of an assistive technology intervention on older adults with disabilities and their informal caregivers: An exploratory randomized controlled trial. American Journal of Physical Medicine and Rehabilitation, 92(4), 297–306. http://www.scopus.com/inward/record.url?eid=2-s2.0-84877929232&partnerID=40&md5=cbcbe2fa42c85ef7b77f465fb84c0a04
Rochette, A., Racine, E., Lefebvre, H., Bastien, J., & Tellier, M. (2014). Actual and ideal services in acute care and rehabilitation for relatives post-stroke from three perspectives: Relatives, stroke clients and health professionals. J Rehabil Med, 46(1), 16–22. https://doi.org/10.2340/16501977-1228
Belle, S. H., Burgio, L., Burns, R., Coon, D., Czaja, S. J., Gallagher-Thompson, D., Gitlin, L. N., Klinger, J., Koepke, K. M., Lee, C. C., Martindale-Adams, J., Nichols, L., Schulz, R., Stahl, S., Stevens, A., Winter, L., Zhang, S., & Health, I. I. (2006). Enhancing the quality of life of dementia caregivers from different ethnic or racial groups: a randomized, controlled trial. Ann Intern Med, 145(10), 727–738. https://www.ncbi.nlm.nih.gov/pubmed/17116917
Tellier, M., Rochette, A., & Lefebvre, H. (2011). Impact of mild stroke on the quality of life of spouses. Int J Rehabil Res, 34(3), 209–214. https://doi.org/10.1097/MRR.0b013e328343d540
Sheets, D. J., Black, K., & Kaye, L. W. (2014). Who cares for caregivers? Evidence-based approaches to family support. J Gerontol Soc Work, 57(6–7), 525–530. https://doi.org/10.1080/01634372.2014.920606
Vincent, C. (2002). Examination of New Environmental Control Applications. Assistive Technology, 14(2), 98–111. http://www.scopus.com/inward/record.url?eid=2-s2.0-1342268863&partnerID=40&md5=8c0cf806753dd9ec8d4ab3a36139859b
Rialle, V., Ollivet, C., Guigui, C., & Herve, C. (2008). What do family caregivers of Alzheimer’s disease patients desire in smart home technologies? Contrasted results of a wide survey. Methods Inf Med, 47(1), 63–69. https://www.ncbi.nlm.nih.gov/pubmed/18213430
Czaja, S. J., Loewenstein, D., Schulz, R., Nair, S. N., & Perdomo, D. (2013). A videophone psychosocial intervention for dementia caregivers. Am J Geriatr Psychiatry, 21(11), 1071–1081. https://doi.org/10.1016/j.jagp.2013.02.019
Oswald, F., & Wahl, H. (2001). Housing in old age: Conceptual remarks and empirical data on place attachment. Bulletin on People-Environment Studies, 19, 8–12.
Bharucha, A. J., Anand, V., Forlizzi, J., Dew, A. M , Reynolds, C. F., Stevens, S., & Wactlar, H. (2009). Intelligent assistive technology applications to dementia care: current capabilities, limitations, and future challenges. Am J Geriatr Psychiatry, 17(2), 88–104. https://doi.org/10.1097/JGP.0b013e318187dde5
for N. Caregiving, N. A. (2009). Caregiving in the U.S. http://www.caregiving.org/data/Caregiving_in_the_US_2009_full_report.pdf
Lee, C. C., Czaja, S. J., & Schulz, R. (2010). The moderating influence of demographic characteristics, social support, and religious coping on the effectiveness of a multicomponent psychosocial caregiver intervention in three racial ethnic groups. J Gerontol B Psychol Sci Soc Sci, 65b(2), 185–194. https://doi.org/10.1093/geronb/gbp131
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