Factors related to perceived burden among caregivers of service members/veterans following TBI. Brickell, T. A., French, L. M., Gartner, R. L., Driscoll, A. E., Wright, M. M., Lippa, S. M., & Lange, R. T. Rehabilitation Psychology, 64(3):307–319, August, 2019. doi abstract bibtex PURPOSE/OBJECTIVE: To examine factors related to perceived caregiving burden in a sample of caregivers assisting service members and veterans (SMVs) across four areas: SMV injury and health status; caregiver life circumstances; caregiver duty and responsibilities; and caregiver needs. Research Method/Design: Participants were 214 caregivers (95.8% female; 86.0% spouse/partner; Age: M = 38.6 years [SD = 10.4]) of SMVs who sustained a mild, moderate, severe, or penetrating traumatic brain injury (TBI). Caregivers were recruited from Walter Reed National Military Medical Center and via community outreach. Participants completed the Caregiver Appraisal Scale, Mayo-Portland Adaptability Inventory-4, and Caregiver Questionnaire. The sample was divided into 2 Caregiver Burden groups: High (n = 138) and Low Burden (n = 76). RESULTS: Factors significantly related to higher levels of perceived burden were (a) experiencing a greater caregiving time commitment now and over time, (b) caring for activities of daily living/instrumental activities of daily living, (c) experiencing an impact of caregiving on employment, income, and out of pocket expenses, (d) parenting more than 1 child, (e) having less time to devote to one's self now and over time, (f) having caregiver needs, and/or (g) assisting a SMV who had incurred a mild TBI; was experiencing greater functional disability; had a posttraumatic stress disorder (PTSD) diagnosis; received mental health and rehabilitation treatment; and/or used an assistive device (all p \textless .05; odds ratios [ORs] = 1.13 to 14.57; ds = .02 to 1.30). CONCLUSIONS/IMPLICATIONS: Providing care for a SMV after a TBI can impose a heavy burden, particularly for caregivers who provide support to SMVs with comorbid mental health problems, such as PTSD. (PsycINFO Database Record (c) 2019 APA, all rights reserved).
@article{brickell_factors_2019,
title = {Factors related to perceived burden among caregivers of service members/veterans following {TBI}},
volume = {64},
issn = {1939-1544},
doi = {10.1037/rep0000272},
abstract = {PURPOSE/OBJECTIVE: To examine factors related to perceived caregiving burden in a sample of caregivers assisting service members and veterans (SMVs) across four areas: SMV injury and health status; caregiver life circumstances; caregiver duty and responsibilities; and caregiver needs. Research Method/Design: Participants were 214 caregivers (95.8\% female; 86.0\% spouse/partner; Age: M = 38.6 years [SD = 10.4]) of SMVs who sustained a mild, moderate, severe, or penetrating traumatic brain injury (TBI). Caregivers were recruited from Walter Reed National Military Medical Center and via community outreach. Participants completed the Caregiver Appraisal Scale, Mayo-Portland Adaptability Inventory-4, and Caregiver Questionnaire. The sample was divided into 2 Caregiver Burden groups: High (n = 138) and Low Burden (n = 76).
RESULTS: Factors significantly related to higher levels of perceived burden were (a) experiencing a greater caregiving time commitment now and over time, (b) caring for activities of daily living/instrumental activities of daily living, (c) experiencing an impact of caregiving on employment, income, and out of pocket expenses, (d) parenting more than 1 child, (e) having less time to devote to one's self now and over time, (f) having caregiver needs, and/or (g) assisting a SMV who had incurred a mild TBI; was experiencing greater functional disability; had a posttraumatic stress disorder (PTSD) diagnosis; received mental health and rehabilitation treatment; and/or used an assistive device (all p {\textless} .05; odds ratios [ORs] = 1.13 to 14.57; ds = .02 to 1.30).
CONCLUSIONS/IMPLICATIONS: Providing care for a SMV after a TBI can impose a heavy burden, particularly for caregivers who provide support to SMVs with comorbid mental health problems, such as PTSD. (PsycINFO Database Record (c) 2019 APA, all rights reserved).},
language = {eng},
number = {3},
journal = {Rehabilitation Psychology},
author = {Brickell, Tracey A. and French, Louis M. and Gartner, Rachel L. and Driscoll, Angela E. and Wright, Megan M. and Lippa, Sara M. and Lange, Rael T.},
month = aug,
year = {2019},
pmid = {30896245},
keywords = {Psychology, TBI},
pages = {307--319}
}
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Research Method/Design: Participants were 214 caregivers (95.8% female; 86.0% spouse/partner; Age: M = 38.6 years [SD = 10.4]) of SMVs who sustained a mild, moderate, severe, or penetrating traumatic brain injury (TBI). Caregivers were recruited from Walter Reed National Military Medical Center and via community outreach. Participants completed the Caregiver Appraisal Scale, Mayo-Portland Adaptability Inventory-4, and Caregiver Questionnaire. The sample was divided into 2 Caregiver Burden groups: High (n = 138) and Low Burden (n = 76). RESULTS: Factors significantly related to higher levels of perceived burden were (a) experiencing a greater caregiving time commitment now and over time, (b) caring for activities of daily living/instrumental activities of daily living, (c) experiencing an impact of caregiving on employment, income, and out of pocket expenses, (d) parenting more than 1 child, (e) having less time to devote to one's self now and over time, (f) having caregiver needs, and/or (g) assisting a SMV who had incurred a mild TBI; was experiencing greater functional disability; had a posttraumatic stress disorder (PTSD) diagnosis; received mental health and rehabilitation treatment; and/or used an assistive device (all p \\textless .05; odds ratios [ORs] = 1.13 to 14.57; ds = .02 to 1.30). CONCLUSIONS/IMPLICATIONS: Providing care for a SMV after a TBI can impose a heavy burden, particularly for caregivers who provide support to SMVs with comorbid mental health problems, such as PTSD. (PsycINFO Database Record (c) 2019 APA, all rights reserved).","language":"eng","number":"3","journal":"Rehabilitation Psychology","author":[{"propositions":[],"lastnames":["Brickell"],"firstnames":["Tracey","A."],"suffixes":[]},{"propositions":[],"lastnames":["French"],"firstnames":["Louis","M."],"suffixes":[]},{"propositions":[],"lastnames":["Gartner"],"firstnames":["Rachel","L."],"suffixes":[]},{"propositions":[],"lastnames":["Driscoll"],"firstnames":["Angela","E."],"suffixes":[]},{"propositions":[],"lastnames":["Wright"],"firstnames":["Megan","M."],"suffixes":[]},{"propositions":[],"lastnames":["Lippa"],"firstnames":["Sara","M."],"suffixes":[]},{"propositions":[],"lastnames":["Lange"],"firstnames":["Rael","T."],"suffixes":[]}],"month":"August","year":"2019","pmid":"30896245","keywords":"Psychology, TBI","pages":"307–319","bibtex":"@article{brickell_factors_2019,\n\ttitle = {Factors related to perceived burden among caregivers of service members/veterans following {TBI}},\n\tvolume = {64},\n\tissn = {1939-1544},\n\tdoi = {10.1037/rep0000272},\n\tabstract = {PURPOSE/OBJECTIVE: To examine factors related to perceived caregiving burden in a sample of caregivers assisting service members and veterans (SMVs) across four areas: SMV injury and health status; caregiver life circumstances; caregiver duty and responsibilities; and caregiver needs. Research Method/Design: Participants were 214 caregivers (95.8\\% female; 86.0\\% spouse/partner; Age: M = 38.6 years [SD = 10.4]) of SMVs who sustained a mild, moderate, severe, or penetrating traumatic brain injury (TBI). Caregivers were recruited from Walter Reed National Military Medical Center and via community outreach. Participants completed the Caregiver Appraisal Scale, Mayo-Portland Adaptability Inventory-4, and Caregiver Questionnaire. The sample was divided into 2 Caregiver Burden groups: High (n = 138) and Low Burden (n = 76).\nRESULTS: Factors significantly related to higher levels of perceived burden were (a) experiencing a greater caregiving time commitment now and over time, (b) caring for activities of daily living/instrumental activities of daily living, (c) experiencing an impact of caregiving on employment, income, and out of pocket expenses, (d) parenting more than 1 child, (e) having less time to devote to one's self now and over time, (f) having caregiver needs, and/or (g) assisting a SMV who had incurred a mild TBI; was experiencing greater functional disability; had a posttraumatic stress disorder (PTSD) diagnosis; received mental health and rehabilitation treatment; and/or used an assistive device (all p {\\textless} .05; odds ratios [ORs] = 1.13 to 14.57; ds = .02 to 1.30).\nCONCLUSIONS/IMPLICATIONS: Providing care for a SMV after a TBI can impose a heavy burden, particularly for caregivers who provide support to SMVs with comorbid mental health problems, such as PTSD. 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