Greta Friedemann-Sánchez
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Greta Friedemann-Sánchez has a total of 78 co-authors. Here are the top co-authors by number of shared publications:
Joan M. Griffin
Robert D. and Patricia E. Kern Mayo Clinic Center for the Science of Health Care Delivery, Mayo Clinic, College of Medicine, Rochester, Minnesota; Division of Health Care Policy and Research, Mayo Clinic, Rochester, Minnesota
6 shared publications- Courtney Harold Van Houtven
Department of Population Health Sciences, Duke University School of Medicine, Durham, NC
5 shared publications - Joan M. Griffin
Mayo Clinic
5 shared publications - Brent C. Taylor
VA Health Service Research & Development (HSR&D) Center for Care Delivery and Outcomes Research (CCDOR), Minneapolis VA Health Care System (VAHCS) Minneapolis Minnesota USA
4 shared publications Michelle van Ryn
Division of Health Care Policy and Research, Mayo Clinic, Rochester, Minnesota; Oregon Health & Science University, Portland, Oregon
4 shared publicationsAgnes C. Jensen
2 shared publications
Latest Publications
- Open Access
- 17 March 2023
- Published by North American Business Press in Journal of Leadership, Accountability and Ethics
- Vol. 20 (1)
Public and Engaged Anthropology: The Legacy of Nina S. de Friedemann
Nina S. de Friedemann (1930-1998) was a public anthropologist. She practiced engaged research, with a view to promoting social justice for the communities with whom she collaborated and studied, and she anticipated the public anthropology of the North Atlantic academia by five decades. A pioneer in AfroColombian studies and in visual anthropology, she documented and defended the cultural contributions of Black populations to the identity of an ethnically diverse Colombia. Friedemann’s fundamental work inspired leaders of the Black communities in their demands that culminated in Law 70 of 1993, also known as the ley de negritudes. Her research materials are housed at the Luis Angel Arango Library under the name Fondo Nina S. de Friedemann, a repository available for study. Using unpublished materials, correspondence, publications, and photographs, Greta Friedemann-Sánchez reflected on three pillars of her mother’s ethical legacy within the contemporary normative framework for the protection of human subjects and the historical context during which Nina S. de Friedemann worked as an anthropologist.
- 17 March 2023
- Published by North American Business Press in Journal of Leadership, Accountability and Ethics
- Vol. 20 (1)
Open AccessPublic and Engaged Anthropology: The Legacy of Nina S. de Friedemann
Nina S. de Friedemann (1930-1998) was a public anthropologist. She practiced engaged research, with a view to promoting social justice for the communities with whom she collaborated and studied, and she anticipated the public anthropology of the North Atlantic academia by five decades. A pioneer in AfroColombian studies and in visual anthropology, she documented and defended the cultural contributions of Black populations to the identity of an ethnically diverse Colombia. Friedemann’s fundamental work inspired leaders of the Black communities in their demands that culminated in Law 70 of 1993, also known as the ley de negritudes. Her research materials are housed at the Luis Angel Arango Library under the name Fondo Nina S. de Friedemann, a repository available for study. Using unpublished materials, correspondence, publications, and photographs, Greta Friedemann-Sánchez reflected on three pillars of her mother’s ethical legacy within the contemporary normative framework for the protection of human subjects and the historical context during which Nina S. de Friedemann worked as an anthropologist.
- 1 November 2018
- Published by Elsevier in Archives of Physical Medicine and Rehabilitation
- Vol. 99 (11) , 2222-2229
The Impact of Stigma on Community Reintegration of Veterans With Traumatic Brain Injury and the Well-Being of Their Caregivers
- 1 November 2018
- Published by Elsevier in Archives of Physical Medicine and Rehabilitation
- Vol. 99 (11) , 2222-2229
The Impact of Stigma on Community Reintegration of Veterans With Traumatic Brain Injury and the Well-Being of Their Caregivers
- 1 December 2017
- Published by Elsevier in Diabetes Research and Clinical Practice
- Vol. 134, 168-177
Mental health and well-being among type 1 diabetes caregivers in India: Evidence from the IDREAM study
- 1 December 2017
- Published by Elsevier in Diabetes Research and Clinical Practice
- Vol. 134, 168-177
Mental health and well-being among type 1 diabetes caregivers in India: Evidence from the IDREAM study
- 15 August 2017
- Published by Hindawi Limited in Pediatric Diabetes
- Vol. 19 (3) , 527-533
Caregiving for children with type 1 diabetes and clinical outcomes in central India: The IDREAM study
Parental care influences outcomes for children's type 1 diabetes (T1D). There is little evidence about the impact of parental caregiving in developing countries, where fixed dose human insulin (conventional) therapy and limited self-monitoring of blood glucose are common. This article investigates whether performance of key T1D management tasks by children or their caregivers impacts hemoglobin A1c (HbA1c). We surveyed the caregivers of 179 children with T1D routinely treated in a specialized diabetes clinic in Maharashtra, India to determine who performs key diabetes care tasks: child or parent. We used linear regression to estimate the relationship between parental caregiving and HbA1c, and how this association varies by child age and time since diagnosis. Caregivers of older children were less involved in care tasks, though caregivers of 11- to 18-year olds performed more care for children diagnosed for a longer duration. Parental involvement in key insulin delivery tasks was associated with lower HbA1c levels for all children. These reductions were greatest among children 11 to 14 years old and diagnosed for less than 2 years: mean HbA1c levels were 8.5% (69 mmol/mol) if the caregiver, and 14.4% (134 mmol/mol) if the child, performed the tasks (P < .05). Parents of children diagnosed with T1D early in life remain involved in care throughout the child's adolescence. Parents of children diagnosed in late childhood and early adolescence are significantly less involved in care, and this is associated with worse glycemic control. Clinics must know who performs care tasks and tailor diabetes education appropriately.
- 15 August 2017
- Published by Hindawi Limited in Pediatric Diabetes
- Vol. 19 (3) , 527-533
Caregiving for children with type 1 diabetes and clinical outcomes in central India: The IDREAM study
Parental care influences outcomes for children's type 1 diabetes (T1D). There is little evidence about the impact of parental caregiving in developing countries, where fixed dose human insulin (conventional) therapy and limited self-monitoring of blood glucose are common. This article investigates whether performance of key T1D management tasks by children or their caregivers impacts hemoglobin A1c (HbA1c). We surveyed the caregivers of 179 children with T1D routinely treated in a specialized diabetes clinic in Maharashtra, India to determine who performs key diabetes care tasks: child or parent. We used linear regression to estimate the relationship between parental caregiving and HbA1c, and how this association varies by child age and time since diagnosis. Caregivers of older children were less involved in care tasks, though caregivers of 11- to 18-year olds performed more care for children diagnosed for a longer duration. Parental involvement in key insulin delivery tasks was associated with lower HbA1c levels for all children. These reductions were greatest among children 11 to 14 years old and diagnosed for less than 2 years: mean HbA1c levels were 8.5% (69 mmol/mol) if the caregiver, and 14.4% (134 mmol/mol) if the child, performed the tasks (P < .05). Parents of children diagnosed with T1D early in life remain involved in care throughout the child's adolescence. Parents of children diagnosed in late childhood and early adolescence are significantly less involved in care, and this is associated with worse glycemic control. Clinics must know who performs care tasks and tailor diabetes education appropriately.
- Open Access
- 1 January 2017
- Published by American Psychological Association (APA) in American Journal of Orthopsychiatry
- Vol. 87 (2) , 139-148
Burden and mental health among caregivers of veterans with traumatic brain injury/polytrauma.
Veterans who survive multiple traumatic injuries, including traumatic brain injuries (TBI), must often rely on family caregivers for ongoing care and support with reintegration. Understanding factors associated with caregiving that help or harm caregivers' health is critical for identifying appropriate and effective interventions that support caregiver health and promote the provision of quality care to veterans. This study utilized cross-sectional data from the Family and Caregiver Experiences Study, a survey of 564 caregivers caring for veterans who served after September 11, 2001, survived TBI/polytrauma during service, and received inpatient rehabilitation care in a Veterans Affairs Polytrauma Rehabilitation Center. Structural equation modeling was used to examine the relationship between caregiver stress (i.e., veterans' neurobehavioral problems and intensity of care required), and caregiver well-being (i.e., caregiver burden and mental health). Analyses also examined how intrapersonal, family or social, and financial resources mediate and moderate the relationship between caregiver stress and well-being. Results indicate that veterans' neurobehavioral problems and intensity of required care were associated with more caregiver burden, and more burden was associated with poor mental health. Intrapersonal and family or social resources mediated the relationship between veteran functioning and mental health. Family or social resources also moderated the relationship between care intensity and burden. The model explained a moderate amount of variability in burden (59%) and a substantial amount in mental health (75%). We conclude that caregivers of veterans with neurobehavioral problems who require intense care are at risk for burden and poor mental health. Increasing resources to bolster family or social resources may reduce risks. (PsycINFO Database Record
- 1 January 2017
- Published by American Psychological Association (APA) in American Journal of Orthopsychiatry
- Vol. 87 (2) , 139-148
Open AccessBurden and mental health among caregivers of veterans with traumatic brain injury/polytrauma.
Veterans who survive multiple traumatic injuries, including traumatic brain injuries (TBI), must often rely on family caregivers for ongoing care and support with reintegration. Understanding factors associated with caregiving that help or harm caregivers' health is critical for identifying appropriate and effective interventions that support caregiver health and promote the provision of quality care to veterans. This study utilized cross-sectional data from the Family and Caregiver Experiences Study, a survey of 564 caregivers caring for veterans who served after September 11, 2001, survived TBI/polytrauma during service, and received inpatient rehabilitation care in a Veterans Affairs Polytrauma Rehabilitation Center. Structural equation modeling was used to examine the relationship between caregiver stress (i.e., veterans' neurobehavioral problems and intensity of care required), and caregiver well-being (i.e., caregiver burden and mental health). Analyses also examined how intrapersonal, family or social, and financial resources mediate and moderate the relationship between caregiver stress and well-being. Results indicate that veterans' neurobehavioral problems and intensity of required care were associated with more caregiver burden, and more burden was associated with poor mental health. Intrapersonal and family or social resources mediated the relationship between veteran functioning and mental health. Family or social resources also moderated the relationship between care intensity and burden. The model explained a moderate amount of variability in burden (59%) and a substantial amount in mental health (75%). We conclude that caregivers of veterans with neurobehavioral problems who require intense care are at risk for burden and poor mental health. Increasing resources to bolster family or social resources may reduce risks. (PsycINFO Database Record
- 24 August 2016
- Published by SAGE Publications in Violence Against Women
- Vol. 23 (12) , 1484-1512
Impact of Domestic Violence on Children’s Education in Colombia: Methodological Challenges
We explore the methodological challenges of estimating the effects of intimate partner violence (IPV) against the mother on the educational outcomes of her children. We tackle the problem of potential endogeneity and non-random selection of children into situations where they are exposed to IPV using non-parametric matching methods and parametric instrumental variable methods. Using Colombia’s 2005 Demographic and Health Survey (DHS), we find that IV and non-IV estimators produce qualitatively similar results at varying degrees of precision, for some educational outcomes. Therefore, exogeneity of IPV to various education outcomes cannot be taken for granted; appropriate methods need to be used to study its causal effects.
- 24 August 2016
- Published by SAGE Publications in Violence Against Women
- Vol. 23 (12) , 1484-1512
Impact of Domestic Violence on Children’s Education in Colombia: Methodological Challenges
We explore the methodological challenges of estimating the effects of intimate partner violence (IPV) against the mother on the educational outcomes of her children. We tackle the problem of potential endogeneity and non-random selection of children into situations where they are exposed to IPV using non-parametric matching methods and parametric instrumental variable methods. Using Colombia’s 2005 Demographic and Health Survey (DHS), we find that IV and non-IV estimators produce qualitatively similar results at varying degrees of precision, for some educational outcomes. Therefore, exogeneity of IPV to various education outcomes cannot be taken for granted; appropriate methods need to be used to study its causal effects.
- 3 August 2016
- Published by Springer Nature
- p. 23-43
Who Will Care for the Elder Caregiver? Outlining Theoretical Approaches and Future Research Questions
- 3 August 2016
- Published by Springer Nature
- p. 23-43
Who Will Care for the Elder Caregiver? Outlining Theoretical Approaches and Future Research Questions
- Open Access
- 1 January 2015
- Published by Wiley in Behavioural Neurology
- Vol. 2015, 1-13
The Relationship between Training and Mental Health among Caregivers of Individuals with Polytrauma
This was a hypothesis-generating exploration of relationships between caregiver training during TBI/polytrauma rehabilitation and caregiver mental health. In this cross-sectional study, 507 informal caregivers to US service members with TBI who received inpatient rehabilitation care in a Veterans Affairs’ Polytrauma Rehabilitation Center from 2001 to 2009 completed a retrospective, self-report survey. Embedded in the survey were measures of caregiver mental health, including the National Institutes of Health’s Patient Reported Outcome Measurement Information System (PROMIS) Anxiety and Depression Short Forms, the Rosenberg Self-Esteem scale, and the Zarit Burden Short Form. Though no groups endorsed clinical levels, mental health symptoms varied by caregiver training category (Trained, Not Trained, and Did Not Need Training). Caregivers who did not receive training on how to navigate healthcare systems endorsed higher depression and burden and lower self-esteem than those who did. Caregivers who did not receive training in supporting their care recipients’ emotions endorsed higher anxiety, depression, and burden and lower self-esteem than those who did. Analyses also suggested a different association between training and mental health based on caregivers’ relationship to the care recipient and the intensity of care recipient needs. Potential hypotheses for testing in future studies raised by these findings are discussed.
- 1 January 2015
- Published by Wiley in Behavioural Neurology
- Vol. 2015, 1-13
Open AccessThe Relationship between Training and Mental Health among Caregivers of Individuals with Polytrauma
This was a hypothesis-generating exploration of relationships between caregiver training during TBI/polytrauma rehabilitation and caregiver mental health. In this cross-sectional study, 507 informal caregivers to US service members with TBI who received inpatient rehabilitation care in a Veterans Affairs’ Polytrauma Rehabilitation Center from 2001 to 2009 completed a retrospective, self-report survey. Embedded in the survey were measures of caregiver mental health, including the National Institutes of Health’s Patient Reported Outcome Measurement Information System (PROMIS) Anxiety and Depression Short Forms, the Rosenberg Self-Esteem scale, and the Zarit Burden Short Form. Though no groups endorsed clinical levels, mental health symptoms varied by caregiver training category (Trained, Not Trained, and Did Not Need Training). Caregivers who did not receive training on how to navigate healthcare systems endorsed higher depression and burden and lower self-esteem than those who did. Caregivers who did not receive training in supporting their care recipients’ emotions endorsed higher anxiety, depression, and burden and lower self-esteem than those who did. Analyses also suggested a different association between training and mental health based on caregivers’ relationship to the care recipient and the intensity of care recipient needs. Potential hypotheses for testing in future studies raised by these findings are discussed.
- Open Access
- 1 November 2012
- Published by SAGE Publications in INQUIRY: The Journal of Health Care Organization, Provision, and Financing
- Vol. 49 (4) , 339-351
Is Policy Well-Targeted to Remedy Financial Strain among Caregivers of Severely Injured U.S. Service Members?
U.S. military service members have sustained severe injuries since the start of the wars in Iraq and Afghanistan. This paper aims to determine the factors associated with financial strain of their caregivers and establish whether recent federal legislation targets caregivers experiencing financial strain. In our national survey, 62.3% of caregivers depleted assets and/or accumulated debt, and 41% of working caregivers left the labor force. If a severely injured veteran needed intensive help, the primary caregiver faced odds 4.63 times higher of leaving the labor force, and used $27,576 more in assets and/or accumulated debt compared to caregivers of veterans needing little or no assistance.
- 1 November 2012
- Published by SAGE Publications in INQUIRY: The Journal of Health Care Organization, Provision, and Financing
- Vol. 49 (4) , 339-351
Open AccessIs Policy Well-Targeted to Remedy Financial Strain among Caregivers of Severely Injured U.S. Service Members?
U.S. military service members have sustained severe injuries since the start of the wars in Iraq and Afghanistan. This paper aims to determine the factors associated with financial strain of their caregivers and establish whether recent federal legislation targets caregivers experiencing financial strain. In our national survey, 62.3% of caregivers depleted assets and/or accumulated debt, and 41% of working caregivers left the labor force. If a severely injured veteran needed intensive help, the primary caregiver faced odds 4.63 times higher of leaving the labor force, and used $27,576 more in assets and/or accumulated debt compared to caregivers of veterans needing little or no assistance.