{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,29]],"date-time":"2026-09-29T09:56:53Z","timestamp":1790675813854,"version":"4.1.0"},"reference-count":100,"publisher":"SAGE Publications","issue":"3","license":[{"start":{"date-parts":[[2026,8,20]],"date-time":"2026-08-20T00:00:00Z","timestamp":1787184000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Journal of Alzheimer\u2019s Disease"],"published-print":{"date-parts":[[2026,10]]},"abstract":"<jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Limited research has examined neurocognitive decline in family caregivers of persons with Alzheimer's disease and Alzheimer's disease-related dementias (AD\/ADRD), despite most caregivers being over 65 and more susceptible to age-related declines due to increased stressors. The lack of insight into how psychosocial factors interact with caregivers\u2019 neurocognitive functioning limits our ability to identify targets for reducing neurocognitive risk.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>Investigate the effects of psychosocial factors on neurocognitive functioning of AD\/ADRD caregivers.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      The caregiver sample (\n                      <jats:italic toggle=\"yes\">n<\/jats:italic>\n                      \u2009=\u200942) consisted predominantly of older adults (\n                      <jats:italic toggle=\"yes\">M<\/jats:italic>\n                      <jats:sub>age<\/jats:sub>\n                      = 69.40,\n                      <jats:italic toggle=\"yes\">SD<\/jats:italic>\n                      <jats:sub>age<\/jats:sub>\n                      = 11.58) who were caring for a spouse (64.3%). On average, caregivers provided 99\u2005h of care per week for several years (\n                      <jats:italic toggle=\"yes\">M<\/jats:italic>\n                      \u2009=\u20093.42,\n                      <jats:italic toggle=\"yes\">SD<\/jats:italic>\n                      \u2009=\u20092.39). Multiple linear regressions were conducted to examine the effects of psychological (i.e., depression, anxiety, pre-death grief, perceived stress) and social (i.e., social support, social network) factors on caregivers\u2019 neurocognitive functioning (i.e., visuospatial memory, verbal memory, processing speed, intelligence, executive functioning).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>Social support significantly predicted visuospatial memory and processing speed. As social support increased, delayed visuospatial memory and processing speed improved when controlling for social network size.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Caregivers may face additional stressors and have limited time or opportunities for social engagement. Social support may be especially important for spousal caregivers losing a primary support source (i.e., spouse). Findings suggest social support is a potential intervention target for reducing caregivers\u2019 risk of neurocognitive decline.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1177\/13872877261476965","type":"journal-article","created":{"date-parts":[[2026,8,20]],"date-time":"2026-08-20T15:02:19Z","timestamp":1787238139000},"page":"1357-1369","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":0,"title":["The impact of psychosocial factors on neurocognitive functioning in family caregivers of persons with Alzheimer's disease and related dementias"],"prefix":"10.1177","volume":"113","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9887-2242","authenticated-orcid":false,"given":"Lauren","family":"Elliott","sequence":"first","affiliation":[{"name":"Texas Tech University"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Emily","family":"Post","sequence":"additional","affiliation":[{"name":"Texas Tech 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