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You searched for subject:(Caregiver Burden). Showing records 1 – 30 of 126 total matches.

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University of Waikato

1. Rose, Wallis. Caregiver Health Related Quality of Life and Burden When Caring for Children with Traumatic Brain Injury .

Degree: 2012, University of Waikato

 Often family members take on the responsibility of caregiver when another family member sustains a traumatic brain injury (TBI). The caregiving role is a stressful… (more)

Subjects/Keywords: Caregiver Burden; Traumatic Brain Injury

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APA (6th Edition):

Rose, W. (2012). Caregiver Health Related Quality of Life and Burden When Caring for Children with Traumatic Brain Injury . (Masters Thesis). University of Waikato. Retrieved from http://hdl.handle.net/10289/7573

Chicago Manual of Style (16th Edition):

Rose, Wallis. “Caregiver Health Related Quality of Life and Burden When Caring for Children with Traumatic Brain Injury .” 2012. Masters Thesis, University of Waikato. Accessed December 13, 2019. http://hdl.handle.net/10289/7573.

MLA Handbook (7th Edition):

Rose, Wallis. “Caregiver Health Related Quality of Life and Burden When Caring for Children with Traumatic Brain Injury .” 2012. Web. 13 Dec 2019.

Vancouver:

Rose W. Caregiver Health Related Quality of Life and Burden When Caring for Children with Traumatic Brain Injury . [Internet] [Masters thesis]. University of Waikato; 2012. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/10289/7573.

Council of Science Editors:

Rose W. Caregiver Health Related Quality of Life and Burden When Caring for Children with Traumatic Brain Injury . [Masters Thesis]. University of Waikato; 2012. Available from: http://hdl.handle.net/10289/7573


University of Canterbury

2. Jones, Ann Judith. Parkinson's Disease, Cognitive Status and Caregiver Outcomes.

Degree: Psychology, 2013, University of Canterbury

 Cognitive impairment in Parkinson’s disease (PD) can impact negatively on caregivers and is associated with carer distress and feelings of burden. To investigate this relationship… (more)

Subjects/Keywords: Parkinson's disease; mild cognitive impairment; caregiver burden

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APA (6th Edition):

Jones, A. J. (2013). Parkinson's Disease, Cognitive Status and Caregiver Outcomes. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/8717

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Jones, Ann Judith. “Parkinson's Disease, Cognitive Status and Caregiver Outcomes.” 2013. Thesis, University of Canterbury. Accessed December 13, 2019. http://hdl.handle.net/10092/8717.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Jones, Ann Judith. “Parkinson's Disease, Cognitive Status and Caregiver Outcomes.” 2013. Web. 13 Dec 2019.

Vancouver:

Jones AJ. Parkinson's Disease, Cognitive Status and Caregiver Outcomes. [Internet] [Thesis]. University of Canterbury; 2013. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/10092/8717.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Jones AJ. Parkinson's Disease, Cognitive Status and Caregiver Outcomes. [Thesis]. University of Canterbury; 2013. Available from: http://hdl.handle.net/10092/8717

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universiteit Utrecht

3. Oors, L.P.A. Prediction of caregiver burden in informal caregivers of frail older people.

Degree: 2015, Universiteit Utrecht

 Background The goal of the Dutch government is to ensure that frail older people can live independently as long as possible. The proportion of frail… (more)

Subjects/Keywords: caregiver burden; frail older people; prediction; determinants

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APA (6th Edition):

Oors, L. P. A. (2015). Prediction of caregiver burden in informal caregivers of frail older people. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/316327

Chicago Manual of Style (16th Edition):

Oors, L P A. “Prediction of caregiver burden in informal caregivers of frail older people.” 2015. Masters Thesis, Universiteit Utrecht. Accessed December 13, 2019. http://dspace.library.uu.nl:8080/handle/1874/316327.

MLA Handbook (7th Edition):

Oors, L P A. “Prediction of caregiver burden in informal caregivers of frail older people.” 2015. Web. 13 Dec 2019.

Vancouver:

Oors LPA. Prediction of caregiver burden in informal caregivers of frail older people. [Internet] [Masters thesis]. Universiteit Utrecht; 2015. [cited 2019 Dec 13]. Available from: http://dspace.library.uu.nl:8080/handle/1874/316327.

Council of Science Editors:

Oors LPA. Prediction of caregiver burden in informal caregivers of frail older people. [Masters Thesis]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/316327


Yale University

4. Philips, Psyche Linnea. The Emotional And Spiritual Wellbeing Of Hospice Patients In Botswana And Sources Of Distress For Their Caregivers.

Degree: MSN, Yale University School of Nursing, 2013, Yale University

  Background: Little regional data exists on the distress of people nearing the end of their lives and their caregivers. Objective: The purpose of this… (more)

Subjects/Keywords: botswana; caregiver burden; gaborone; hospice; palliative; QODD

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APA (6th Edition):

Philips, P. L. (2013). The Emotional And Spiritual Wellbeing Of Hospice Patients In Botswana And Sources Of Distress For Their Caregivers. (Masters Thesis). Yale University. Retrieved from https://elischolar.library.yale.edu/ysndt/1009

Chicago Manual of Style (16th Edition):

Philips, Psyche Linnea. “The Emotional And Spiritual Wellbeing Of Hospice Patients In Botswana And Sources Of Distress For Their Caregivers.” 2013. Masters Thesis, Yale University. Accessed December 13, 2019. https://elischolar.library.yale.edu/ysndt/1009.

MLA Handbook (7th Edition):

Philips, Psyche Linnea. “The Emotional And Spiritual Wellbeing Of Hospice Patients In Botswana And Sources Of Distress For Their Caregivers.” 2013. Web. 13 Dec 2019.

Vancouver:

Philips PL. The Emotional And Spiritual Wellbeing Of Hospice Patients In Botswana And Sources Of Distress For Their Caregivers. [Internet] [Masters thesis]. Yale University; 2013. [cited 2019 Dec 13]. Available from: https://elischolar.library.yale.edu/ysndt/1009.

Council of Science Editors:

Philips PL. The Emotional And Spiritual Wellbeing Of Hospice Patients In Botswana And Sources Of Distress For Their Caregivers. [Masters Thesis]. Yale University; 2013. Available from: https://elischolar.library.yale.edu/ysndt/1009


Oklahoma State University

5. Wolfe-Christensen, Cortney. Relationships of Parental Uncertainty and Caregiver Burden to Adjustment Outcomes in Children with Cancer: the Moderating Role of Parenting Stress.

Degree: Department of Psychology, 2009, Oklahoma State University

 The current study sought to determine whether levels of parental uncertainty and caregiver burden, as reported by parents of children with pediatric cancer, were related… (more)

Subjects/Keywords: adjustment; caregiver burden; parenting stress; pediatric oncology

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APA (6th Edition):

Wolfe-Christensen, C. (2009). Relationships of Parental Uncertainty and Caregiver Burden to Adjustment Outcomes in Children with Cancer: the Moderating Role of Parenting Stress. (Thesis). Oklahoma State University. Retrieved from http://hdl.handle.net/11244/6990

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wolfe-Christensen, Cortney. “Relationships of Parental Uncertainty and Caregiver Burden to Adjustment Outcomes in Children with Cancer: the Moderating Role of Parenting Stress.” 2009. Thesis, Oklahoma State University. Accessed December 13, 2019. http://hdl.handle.net/11244/6990.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wolfe-Christensen, Cortney. “Relationships of Parental Uncertainty and Caregiver Burden to Adjustment Outcomes in Children with Cancer: the Moderating Role of Parenting Stress.” 2009. Web. 13 Dec 2019.

Vancouver:

Wolfe-Christensen C. Relationships of Parental Uncertainty and Caregiver Burden to Adjustment Outcomes in Children with Cancer: the Moderating Role of Parenting Stress. [Internet] [Thesis]. Oklahoma State University; 2009. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/11244/6990.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wolfe-Christensen C. Relationships of Parental Uncertainty and Caregiver Burden to Adjustment Outcomes in Children with Cancer: the Moderating Role of Parenting Stress. [Thesis]. Oklahoma State University; 2009. Available from: http://hdl.handle.net/11244/6990

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

6. Logan, Bridget. Living With a Depressed Partner.

Degree: PhD, Nursing, 2011, U of Massachusetts : PhD

  Individuals who live with depressed partners have increased rates of anxiety, depression, and difficult coping. They experience greater burdens of parenting and financial responsibilities,… (more)

Subjects/Keywords: Caregiver Burden; Depression; Nondepressed Partner; Nursing

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APA (6th Edition):

Logan, B. (2011). Living With a Depressed Partner. (Doctoral Dissertation). U of Massachusetts : PhD. Retrieved from https://scholarworks.umass.edu/open_access_dissertations/340

Chicago Manual of Style (16th Edition):

Logan, Bridget. “Living With a Depressed Partner.” 2011. Doctoral Dissertation, U of Massachusetts : PhD. Accessed December 13, 2019. https://scholarworks.umass.edu/open_access_dissertations/340.

MLA Handbook (7th Edition):

Logan, Bridget. “Living With a Depressed Partner.” 2011. Web. 13 Dec 2019.

Vancouver:

Logan B. Living With a Depressed Partner. [Internet] [Doctoral dissertation]. U of Massachusetts : PhD; 2011. [cited 2019 Dec 13]. Available from: https://scholarworks.umass.edu/open_access_dissertations/340.

Council of Science Editors:

Logan B. Living With a Depressed Partner. [Doctoral Dissertation]. U of Massachusetts : PhD; 2011. Available from: https://scholarworks.umass.edu/open_access_dissertations/340


University of South Africa

7. Makura, Helena. Factors influencing the burden of caregivers of children with cerebral palsy in Namibia .

Degree: 2018, University of South Africa

 The aim of this study was to investigate factors that influence the burden of caregiving on the caregivers of children with cerebral palsy (CP) in… (more)

Subjects/Keywords: Burden; Caregiver; Caregiving; Cerebral palsy; Children; Factors

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APA (6th Edition):

Makura, H. (2018). Factors influencing the burden of caregivers of children with cerebral palsy in Namibia . (Masters Thesis). University of South Africa. Retrieved from http://hdl.handle.net/10500/25326

Chicago Manual of Style (16th Edition):

Makura, Helena. “Factors influencing the burden of caregivers of children with cerebral palsy in Namibia .” 2018. Masters Thesis, University of South Africa. Accessed December 13, 2019. http://hdl.handle.net/10500/25326.

MLA Handbook (7th Edition):

Makura, Helena. “Factors influencing the burden of caregivers of children with cerebral palsy in Namibia .” 2018. Web. 13 Dec 2019.

Vancouver:

Makura H. Factors influencing the burden of caregivers of children with cerebral palsy in Namibia . [Internet] [Masters thesis]. University of South Africa; 2018. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/10500/25326.

Council of Science Editors:

Makura H. Factors influencing the burden of caregivers of children with cerebral palsy in Namibia . [Masters Thesis]. University of South Africa; 2018. Available from: http://hdl.handle.net/10500/25326


University of Miami

8. Suro, Giulia C. Ethnic/Racial Differences in the Experience of Burden and Psychological Outcomes for Caregivers of Patients with Schizophrenia: the Influence of Family Cohesion and Interdependence.

Degree: MS, Psychology (Arts and Sciences), 2011, University of Miami

  Research has demonstrated that taking care of a patient with schizophrenia has serious mental health costs to caregivers including high levels of burden and… (more)

Subjects/Keywords: Schizophrenia; caregiver burden; family cohesion; interdependence

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APA (6th Edition):

Suro, G. C. (2011). Ethnic/Racial Differences in the Experience of Burden and Psychological Outcomes for Caregivers of Patients with Schizophrenia: the Influence of Family Cohesion and Interdependence. (Thesis). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_theses/274

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Suro, Giulia C. “Ethnic/Racial Differences in the Experience of Burden and Psychological Outcomes for Caregivers of Patients with Schizophrenia: the Influence of Family Cohesion and Interdependence.” 2011. Thesis, University of Miami. Accessed December 13, 2019. https://scholarlyrepository.miami.edu/oa_theses/274.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Suro, Giulia C. “Ethnic/Racial Differences in the Experience of Burden and Psychological Outcomes for Caregivers of Patients with Schizophrenia: the Influence of Family Cohesion and Interdependence.” 2011. Web. 13 Dec 2019.

Vancouver:

Suro GC. Ethnic/Racial Differences in the Experience of Burden and Psychological Outcomes for Caregivers of Patients with Schizophrenia: the Influence of Family Cohesion and Interdependence. [Internet] [Thesis]. University of Miami; 2011. [cited 2019 Dec 13]. Available from: https://scholarlyrepository.miami.edu/oa_theses/274.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Suro GC. Ethnic/Racial Differences in the Experience of Burden and Psychological Outcomes for Caregivers of Patients with Schizophrenia: the Influence of Family Cohesion and Interdependence. [Thesis]. University of Miami; 2011. Available from: https://scholarlyrepository.miami.edu/oa_theses/274

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Ohio University

9. VanMeter, Adrianna J. The Impact of Dementia Caregiving on Caregiver Cognitive Health.

Degree: PhD, Clinical Psychology (Arts and Sciences), 2017, Ohio University

 Providing care for individuals with dementia (IWD) is associated with significant burden and negative health outcomes. While it is well-documented that caregiving has negative effects… (more)

Subjects/Keywords: Psychology; Clinical Psychology; Dementia caregivers; caregiver stress; caregiver burden; cognition

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APA (6th Edition):

VanMeter, A. J. (2017). The Impact of Dementia Caregiving on Caregiver Cognitive Health. (Doctoral Dissertation). Ohio University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1508854228522232

Chicago Manual of Style (16th Edition):

VanMeter, Adrianna J. “The Impact of Dementia Caregiving on Caregiver Cognitive Health.” 2017. Doctoral Dissertation, Ohio University. Accessed December 13, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1508854228522232.

MLA Handbook (7th Edition):

VanMeter, Adrianna J. “The Impact of Dementia Caregiving on Caregiver Cognitive Health.” 2017. Web. 13 Dec 2019.

Vancouver:

VanMeter AJ. The Impact of Dementia Caregiving on Caregiver Cognitive Health. [Internet] [Doctoral dissertation]. Ohio University; 2017. [cited 2019 Dec 13]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1508854228522232.

Council of Science Editors:

VanMeter AJ. The Impact of Dementia Caregiving on Caregiver Cognitive Health. [Doctoral Dissertation]. Ohio University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1508854228522232


University of Louisville

10. Holley, Caitlin. Anticipatory grief in the context of dementia caregiving.

Degree: PhD, 2009, University of Louisville

  The current study investigated the nature of anticipatory grief in a sample of dementia caregivers, and examined the relationship between anticipatory grief and caregiver(more)

Subjects/Keywords: Anticipatory grief; Caregiver grief; Dementia caregiving; Caregiver burden; Grief

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APA (6th Edition):

Holley, C. (2009). Anticipatory grief in the context of dementia caregiving. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/625 ; https://ir.library.louisville.edu/etd/625

Chicago Manual of Style (16th Edition):

Holley, Caitlin. “Anticipatory grief in the context of dementia caregiving.” 2009. Doctoral Dissertation, University of Louisville. Accessed December 13, 2019. 10.18297/etd/625 ; https://ir.library.louisville.edu/etd/625.

MLA Handbook (7th Edition):

Holley, Caitlin. “Anticipatory grief in the context of dementia caregiving.” 2009. Web. 13 Dec 2019.

Vancouver:

Holley C. Anticipatory grief in the context of dementia caregiving. [Internet] [Doctoral dissertation]. University of Louisville; 2009. [cited 2019 Dec 13]. Available from: 10.18297/etd/625 ; https://ir.library.louisville.edu/etd/625.

Council of Science Editors:

Holley C. Anticipatory grief in the context of dementia caregiving. [Doctoral Dissertation]. University of Louisville; 2009. Available from: 10.18297/etd/625 ; https://ir.library.louisville.edu/etd/625


Queensland University of Technology

11. Truong, Quang Trung. The quality of life and caregiving burden among caregivers of people with dementia in Hanoi, Bac Ninh and Hai Phong, Vietnam.

Degree: 2015, Queensland University of Technology

 This three phase study aimed to describe dementia carer's quality of life (QoL) and perceived burden, and explore the associations between family carer characteristics, burden(more)

Subjects/Keywords: Quality of life; Caregiving burden; dementia caregiver; Vietnam; Vietnamese dementia caregiver

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APA (6th Edition):

Truong, Q. T. (2015). The quality of life and caregiving burden among caregivers of people with dementia in Hanoi, Bac Ninh and Hai Phong, Vietnam. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/82287/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Truong, Quang Trung. “The quality of life and caregiving burden among caregivers of people with dementia in Hanoi, Bac Ninh and Hai Phong, Vietnam.” 2015. Thesis, Queensland University of Technology. Accessed December 13, 2019. https://eprints.qut.edu.au/82287/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Truong, Quang Trung. “The quality of life and caregiving burden among caregivers of people with dementia in Hanoi, Bac Ninh and Hai Phong, Vietnam.” 2015. Web. 13 Dec 2019.

Vancouver:

Truong QT. The quality of life and caregiving burden among caregivers of people with dementia in Hanoi, Bac Ninh and Hai Phong, Vietnam. [Internet] [Thesis]. Queensland University of Technology; 2015. [cited 2019 Dec 13]. Available from: https://eprints.qut.edu.au/82287/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Truong QT. The quality of life and caregiving burden among caregivers of people with dementia in Hanoi, Bac Ninh and Hai Phong, Vietnam. [Thesis]. Queensland University of Technology; 2015. Available from: https://eprints.qut.edu.au/82287/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Northeastern University

12. Gallant, Kelly. Caregiver reactions in pulmonary hypertension.

Degree: PhD, School of Nursing, 2017, Northeastern University

 This dissertation contains a modified Walker and Avant (2005) concept analysis on caregiver reactions, a review of empirical referents, and a qualitative phenomenological investigation into… (more)

Subjects/Keywords: caregiver burden; caregiver reactions; concept analysis; informal caregivers; psychometrics; pulmonary hypertension

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APA (6th Edition):

Gallant, K. (2017). Caregiver reactions in pulmonary hypertension. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20272508

Chicago Manual of Style (16th Edition):

Gallant, Kelly. “Caregiver reactions in pulmonary hypertension.” 2017. Doctoral Dissertation, Northeastern University. Accessed December 13, 2019. http://hdl.handle.net/2047/D20272508.

MLA Handbook (7th Edition):

Gallant, Kelly. “Caregiver reactions in pulmonary hypertension.” 2017. Web. 13 Dec 2019.

Vancouver:

Gallant K. Caregiver reactions in pulmonary hypertension. [Internet] [Doctoral dissertation]. Northeastern University; 2017. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/2047/D20272508.

Council of Science Editors:

Gallant K. Caregiver reactions in pulmonary hypertension. [Doctoral Dissertation]. Northeastern University; 2017. Available from: http://hdl.handle.net/2047/D20272508


Boston University

13. Ness-Cohn, Avital. The post-stroke discharge planning toolkit: helping caregivers of stroke survivors navigate the transition from inpatient setting to home.

Degree: 2019, Boston University

 Stroke is the leading cause of long-term disability in the United States and often leaves individuals with physical and cognitive deficits. Stroke survivors are discharging… (more)

Subjects/Keywords: Occupational therapy; Caregiver burden; Caregiver burnout; Cognitive strategies; Toolbox; Transition

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APA (6th Edition):

Ness-Cohn, A. (2019). The post-stroke discharge planning toolkit: helping caregivers of stroke survivors navigate the transition from inpatient setting to home. (Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/38144

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ness-Cohn, Avital. “The post-stroke discharge planning toolkit: helping caregivers of stroke survivors navigate the transition from inpatient setting to home.” 2019. Thesis, Boston University. Accessed December 13, 2019. http://hdl.handle.net/2144/38144.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ness-Cohn, Avital. “The post-stroke discharge planning toolkit: helping caregivers of stroke survivors navigate the transition from inpatient setting to home.” 2019. Web. 13 Dec 2019.

Vancouver:

Ness-Cohn A. The post-stroke discharge planning toolkit: helping caregivers of stroke survivors navigate the transition from inpatient setting to home. [Internet] [Thesis]. Boston University; 2019. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/2144/38144.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ness-Cohn A. The post-stroke discharge planning toolkit: helping caregivers of stroke survivors navigate the transition from inpatient setting to home. [Thesis]. Boston University; 2019. Available from: http://hdl.handle.net/2144/38144

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Texas State University – San Marcos

14. Vannoy, Teresa A. BRFSS 2015-2017: Exploring the Burden of Caring For Others.

Degree: MS, Sociology, 2018, Texas State University – San Marcos

 Recognizing the growing public health need for informal care, the U.S. Centers for Disease Control & Prevention (CDC) commissioned an expert panel to develop a… (more)

Subjects/Keywords: BRFSS; Caregiver Burden; Caregiver Module; Medicine and psychology; Health surveys; Caregivers

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APA (6th Edition):

Vannoy, T. A. (2018). BRFSS 2015-2017: Exploring the Burden of Caring For Others. (Masters Thesis). Texas State University – San Marcos. Retrieved from https://digital.library.txstate.edu/handle/10877/7781

Chicago Manual of Style (16th Edition):

Vannoy, Teresa A. “BRFSS 2015-2017: Exploring the Burden of Caring For Others.” 2018. Masters Thesis, Texas State University – San Marcos. Accessed December 13, 2019. https://digital.library.txstate.edu/handle/10877/7781.

MLA Handbook (7th Edition):

Vannoy, Teresa A. “BRFSS 2015-2017: Exploring the Burden of Caring For Others.” 2018. Web. 13 Dec 2019.

Vancouver:

Vannoy TA. BRFSS 2015-2017: Exploring the Burden of Caring For Others. [Internet] [Masters thesis]. Texas State University – San Marcos; 2018. [cited 2019 Dec 13]. Available from: https://digital.library.txstate.edu/handle/10877/7781.

Council of Science Editors:

Vannoy TA. BRFSS 2015-2017: Exploring the Burden of Caring For Others. [Masters Thesis]. Texas State University – San Marcos; 2018. Available from: https://digital.library.txstate.edu/handle/10877/7781


University of Guelph

15. Ofosu, Antonia. The Association of Caregiver Burden with Perceived Stress and Youth Symptomatology .

Degree: 2018, University of Guelph

 This exploratory study was focused on caregivers’ burden and stress in families with youths hospitalized for severe psychiatric disorders. The study utilized survey research on… (more)

Subjects/Keywords: Caregiver burden; Caregiver burden among parents with youth with psychiatric disorders; Perceived parental stress among caregivers with hospitalized youth; Caregiver burden and perceived parental stress; Caregivers' perspectives on burden; Association of caregiver burden with youth psychiatric symptoms; Caregiver burden and youth psychiatric symptoms; Caregiver burden among parents with youth with severe psychiatric symptoms; Caregivers' views on burden and youth psychiatric hospitalization

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APA (6th Edition):

Ofosu, A. (2018). The Association of Caregiver Burden with Perceived Stress and Youth Symptomatology . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/12164

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ofosu, Antonia. “The Association of Caregiver Burden with Perceived Stress and Youth Symptomatology .” 2018. Thesis, University of Guelph. Accessed December 13, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/12164.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ofosu, Antonia. “The Association of Caregiver Burden with Perceived Stress and Youth Symptomatology .” 2018. Web. 13 Dec 2019.

Vancouver:

Ofosu A. The Association of Caregiver Burden with Perceived Stress and Youth Symptomatology . [Internet] [Thesis]. University of Guelph; 2018. [cited 2019 Dec 13]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/12164.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ofosu A. The Association of Caregiver Burden with Perceived Stress and Youth Symptomatology . [Thesis]. University of Guelph; 2018. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/12164

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

16. Holdsworth, Jason Keith. Burden of care impacting family caregivers of dependent community-dwelling older adults in rural and urban settings of Southern Turkey.

Degree: 2013, Technische Universität Dortmund

 Population ageing is taking place at an unprecedented rate in Turkey and expected to continue through 2050. This study represents an important first initiative aimed… (more)

Subjects/Keywords: Antalya home care survey; caregiver burden; primary family caregiver; rural, urban environments; Southern Turkey; 150

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APA (6th Edition):

Holdsworth, J. K. (2013). Burden of care impacting family caregivers of dependent community-dwelling older adults in rural and urban settings of Southern Turkey. (Thesis). Technische Universität Dortmund. Retrieved from http://hdl.handle.net/2003/30138

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Holdsworth, Jason Keith. “Burden of care impacting family caregivers of dependent community-dwelling older adults in rural and urban settings of Southern Turkey.” 2013. Thesis, Technische Universität Dortmund. Accessed December 13, 2019. http://hdl.handle.net/2003/30138.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Holdsworth, Jason Keith. “Burden of care impacting family caregivers of dependent community-dwelling older adults in rural and urban settings of Southern Turkey.” 2013. Web. 13 Dec 2019.

Vancouver:

Holdsworth JK. Burden of care impacting family caregivers of dependent community-dwelling older adults in rural and urban settings of Southern Turkey. [Internet] [Thesis]. Technische Universität Dortmund; 2013. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/2003/30138.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Holdsworth JK. Burden of care impacting family caregivers of dependent community-dwelling older adults in rural and urban settings of Southern Turkey. [Thesis]. Technische Universität Dortmund; 2013. Available from: http://hdl.handle.net/2003/30138

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Virginia Commonwealth University

17. Smith, Erin. A cross-cultural examination of the relations among Parkinson’s disease impairments, caregiver burden and mental health, and family dynamics in Mexico and the United States.

Degree: PhD, Health Psychology, 2019, Virginia Commonwealth University

  Parkinson’s Disease (PD) is a common progressive neurodegenerative disorder that leads to both physical and cognitive impairment over time. Eventually, these impairments may include… (more)

Subjects/Keywords: Parkinson's disease; caregiving; caregiver burden; caregiver mental health; family dynamics; Health Psychology; Multicultural Psychology

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APA (6th Edition):

Smith, E. (2019). A cross-cultural examination of the relations among Parkinson’s disease impairments, caregiver burden and mental health, and family dynamics in Mexico and the United States. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/5814

Chicago Manual of Style (16th Edition):

Smith, Erin. “A cross-cultural examination of the relations among Parkinson’s disease impairments, caregiver burden and mental health, and family dynamics in Mexico and the United States.” 2019. Doctoral Dissertation, Virginia Commonwealth University. Accessed December 13, 2019. https://scholarscompass.vcu.edu/etd/5814.

MLA Handbook (7th Edition):

Smith, Erin. “A cross-cultural examination of the relations among Parkinson’s disease impairments, caregiver burden and mental health, and family dynamics in Mexico and the United States.” 2019. Web. 13 Dec 2019.

Vancouver:

Smith E. A cross-cultural examination of the relations among Parkinson’s disease impairments, caregiver burden and mental health, and family dynamics in Mexico and the United States. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2019. [cited 2019 Dec 13]. Available from: https://scholarscompass.vcu.edu/etd/5814.

Council of Science Editors:

Smith E. A cross-cultural examination of the relations among Parkinson’s disease impairments, caregiver burden and mental health, and family dynamics in Mexico and the United States. [Doctoral Dissertation]. Virginia Commonwealth University; 2019. Available from: https://scholarscompass.vcu.edu/etd/5814


University of New South Wales

18. Seeher, Katrin. The psychosocial effects of becoming a carer: Predicting psychological distress and caregiver burden in family members and friends of older people with normal cognitive function, mild cognitive impairment and dementia over time.

Degree: Psychiatry, 2015, University of New South Wales

 Dementia caregiving has been linked to negative physical and mental health outcomes for carers. However, the evidence is primarily based on cross-sectional research, with only… (more)

Subjects/Keywords: Dementia; Caregiver; Mild cognitive impairment; Psychological distress; Caregiver burden; Family; Longitudinal; Latent growth curve

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APA (6th Edition):

Seeher, K. (2015). The psychosocial effects of becoming a carer: Predicting psychological distress and caregiver burden in family members and friends of older people with normal cognitive function, mild cognitive impairment and dementia over time. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/55026 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36386/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Seeher, Katrin. “The psychosocial effects of becoming a carer: Predicting psychological distress and caregiver burden in family members and friends of older people with normal cognitive function, mild cognitive impairment and dementia over time.” 2015. Doctoral Dissertation, University of New South Wales. Accessed December 13, 2019. http://handle.unsw.edu.au/1959.4/55026 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36386/SOURCE02?view=true.

MLA Handbook (7th Edition):

Seeher, Katrin. “The psychosocial effects of becoming a carer: Predicting psychological distress and caregiver burden in family members and friends of older people with normal cognitive function, mild cognitive impairment and dementia over time.” 2015. Web. 13 Dec 2019.

Vancouver:

Seeher K. The psychosocial effects of becoming a carer: Predicting psychological distress and caregiver burden in family members and friends of older people with normal cognitive function, mild cognitive impairment and dementia over time. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2019 Dec 13]. Available from: http://handle.unsw.edu.au/1959.4/55026 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36386/SOURCE02?view=true.

Council of Science Editors:

Seeher K. The psychosocial effects of becoming a carer: Predicting psychological distress and caregiver burden in family members and friends of older people with normal cognitive function, mild cognitive impairment and dementia over time. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/55026 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:36386/SOURCE02?view=true


University of Kansas

19. Rigby, Taylor. DIFFERENCES IN CAREGIVER GRIEF AND BURDEN BETWEEN DEMENTIA WITH LEWY BODIES, DEMENTIA OF THE ALZHEIMER’S TYPE, AND DEMENTIA ASSOCIATED WITH PARKINSON’S DISEASE.

Degree: MA, Psychology, 2016, University of Kansas

 Background: Caregiving for dementia has been associated with increased grief and burden. Dementia with Lewy Bodies (DLB) is the second most common form of dementia;… (more)

Subjects/Keywords: Clinical psychology; Gerontology; Psychology; caregiver; caregiver burden; caregiver grief; dementia; dementia with lewy bodies; lewy body dementia

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APA (6th Edition):

Rigby, T. (2016). DIFFERENCES IN CAREGIVER GRIEF AND BURDEN BETWEEN DEMENTIA WITH LEWY BODIES, DEMENTIA OF THE ALZHEIMER’S TYPE, AND DEMENTIA ASSOCIATED WITH PARKINSON’S DISEASE. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/25431

Chicago Manual of Style (16th Edition):

Rigby, Taylor. “DIFFERENCES IN CAREGIVER GRIEF AND BURDEN BETWEEN DEMENTIA WITH LEWY BODIES, DEMENTIA OF THE ALZHEIMER’S TYPE, AND DEMENTIA ASSOCIATED WITH PARKINSON’S DISEASE.” 2016. Masters Thesis, University of Kansas. Accessed December 13, 2019. http://hdl.handle.net/1808/25431.

MLA Handbook (7th Edition):

Rigby, Taylor. “DIFFERENCES IN CAREGIVER GRIEF AND BURDEN BETWEEN DEMENTIA WITH LEWY BODIES, DEMENTIA OF THE ALZHEIMER’S TYPE, AND DEMENTIA ASSOCIATED WITH PARKINSON’S DISEASE.” 2016. Web. 13 Dec 2019.

Vancouver:

Rigby T. DIFFERENCES IN CAREGIVER GRIEF AND BURDEN BETWEEN DEMENTIA WITH LEWY BODIES, DEMENTIA OF THE ALZHEIMER’S TYPE, AND DEMENTIA ASSOCIATED WITH PARKINSON’S DISEASE. [Internet] [Masters thesis]. University of Kansas; 2016. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/1808/25431.

Council of Science Editors:

Rigby T. DIFFERENCES IN CAREGIVER GRIEF AND BURDEN BETWEEN DEMENTIA WITH LEWY BODIES, DEMENTIA OF THE ALZHEIMER’S TYPE, AND DEMENTIA ASSOCIATED WITH PARKINSON’S DISEASE. [Masters Thesis]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/25431

20. Winge, Moa Malmqvist. Att tappa fotfästet : en litteraturstudie: Närståendes upplevelser och erfarenheter av att vårda en person som drabbats av stroke.

Degree: Health Science, 2012, University of Borås

Stroke är den tredje vanligaste dödsorsaken i Sverige och risken för att insjukna ökar med stigande ålder. Vid stroke har personen drabbats antingen av… (more)

Subjects/Keywords: stroke; stroke survivor; spouses; caring; informal caregiver; experiences; caregiver burden; caregiver support; Medical and Health Sciences; Medicin och hälsovetenskap

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APA (6th Edition):

Winge, M. M. (2012). Att tappa fotfästet : en litteraturstudie: Närståendes upplevelser och erfarenheter av att vårda en person som drabbats av stroke. (Thesis). University of Borås. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:hb:diva-16679

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Winge, Moa Malmqvist. “Att tappa fotfästet : en litteraturstudie: Närståendes upplevelser och erfarenheter av att vårda en person som drabbats av stroke.” 2012. Thesis, University of Borås. Accessed December 13, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:hb:diva-16679.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Winge, Moa Malmqvist. “Att tappa fotfästet : en litteraturstudie: Närståendes upplevelser och erfarenheter av att vårda en person som drabbats av stroke.” 2012. Web. 13 Dec 2019.

Vancouver:

Winge MM. Att tappa fotfästet : en litteraturstudie: Närståendes upplevelser och erfarenheter av att vårda en person som drabbats av stroke. [Internet] [Thesis]. University of Borås; 2012. [cited 2019 Dec 13]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hb:diva-16679.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Winge MM. Att tappa fotfästet : en litteraturstudie: Närståendes upplevelser och erfarenheter av att vårda en person som drabbats av stroke. [Thesis]. University of Borås; 2012. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hb:diva-16679

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


The Ohio State University

21. Hand, Brittany Nicole. Caregiver Burden, Participation, and Sensory Subtypes in Children with Autism.

Degree: PhD, Health and Rehabilitation Sciences, 2016, The Ohio State University

 Fifty-three percent of occupational therapists lack confidence when working with the autism population and 60% consider autism spectrum disorders (ASD) to be more challenging to… (more)

Subjects/Keywords: Occupational Therapy; Rehabilitation; Caregiver Burden, Participation, Sensory Subtypes, Children with Autism

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APA (6th Edition):

Hand, B. N. (2016). Caregiver Burden, Participation, and Sensory Subtypes in Children with Autism. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1479891856606551

Chicago Manual of Style (16th Edition):

Hand, Brittany Nicole. “Caregiver Burden, Participation, and Sensory Subtypes in Children with Autism.” 2016. Doctoral Dissertation, The Ohio State University. Accessed December 13, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1479891856606551.

MLA Handbook (7th Edition):

Hand, Brittany Nicole. “Caregiver Burden, Participation, and Sensory Subtypes in Children with Autism.” 2016. Web. 13 Dec 2019.

Vancouver:

Hand BN. Caregiver Burden, Participation, and Sensory Subtypes in Children with Autism. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2019 Dec 13]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1479891856606551.

Council of Science Editors:

Hand BN. Caregiver Burden, Participation, and Sensory Subtypes in Children with Autism. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1479891856606551


Universidade do Rio Grande do Sul

22. Marinho, Nathercia Estevam. Impacto da demência e dos sintomas neuropsiquiátricos sobre a sobrecarga do cuidador na doença de Parkinson.

Degree: 2017, Universidade do Rio Grande do Sul

OBJETIVO: O objetivo do estudo foi avaliar a associação entre sobrecarga do cuidador, demência e sintomas neuropsiquiátricos entre cuidadores familiares de pacientes com doença de… (more)

Subjects/Keywords: Doença de Parkinson; Disease; Demência; Caregiver burden; Cuidadores; Neuropsychiatric Symptoms; Insanity

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APA (6th Edition):

Marinho, N. E. (2017). Impacto da demência e dos sintomas neuropsiquiátricos sobre a sobrecarga do cuidador na doença de Parkinson. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/178964

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Marinho, Nathercia Estevam. “Impacto da demência e dos sintomas neuropsiquiátricos sobre a sobrecarga do cuidador na doença de Parkinson.” 2017. Thesis, Universidade do Rio Grande do Sul. Accessed December 13, 2019. http://hdl.handle.net/10183/178964.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Marinho, Nathercia Estevam. “Impacto da demência e dos sintomas neuropsiquiátricos sobre a sobrecarga do cuidador na doença de Parkinson.” 2017. Web. 13 Dec 2019.

Vancouver:

Marinho NE. Impacto da demência e dos sintomas neuropsiquiátricos sobre a sobrecarga do cuidador na doença de Parkinson. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2017. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/10183/178964.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Marinho NE. Impacto da demência e dos sintomas neuropsiquiátricos sobre a sobrecarga do cuidador na doença de Parkinson. [Thesis]. Universidade do Rio Grande do Sul; 2017. Available from: http://hdl.handle.net/10183/178964

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

23. GIOVANNA DEL GRANDE DA SILVA ALVES. SOBRECARGA E FATORES ASSOCIADOS EM CUIDADORES DE JOVENS ENTRE 18 E 24 ANOS COM TRANSTORNO DE HUMOR BIPOLAR E UNIPOLAR.

Degree: 2011, Universidade Catolica de Pelotas

Background: Caregiver burden has been associated both with the caregivers need for support and information, and the caregivers mental disorders. However, there are not quantitative… (more)

Subjects/Keywords: transtorno bipolar; depressão; sobrecarga; MEDICINA; Burden; Caregiver; Bipolar Disorder; cuidadores; Depression

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APA (6th Edition):

ALVES, G. D. G. D. S. (2011). SOBRECARGA E FATORES ASSOCIADOS EM CUIDADORES DE JOVENS ENTRE 18 E 24 ANOS COM TRANSTORNO DE HUMOR BIPOLAR E UNIPOLAR. (Thesis). Universidade Catolica de Pelotas. Retrieved from http://biblioteca.ucpel.tche.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=277

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

ALVES, GIOVANNA DEL GRANDE DA SILVA. “SOBRECARGA E FATORES ASSOCIADOS EM CUIDADORES DE JOVENS ENTRE 18 E 24 ANOS COM TRANSTORNO DE HUMOR BIPOLAR E UNIPOLAR.” 2011. Thesis, Universidade Catolica de Pelotas. Accessed December 13, 2019. http://biblioteca.ucpel.tche.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=277.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

ALVES, GIOVANNA DEL GRANDE DA SILVA. “SOBRECARGA E FATORES ASSOCIADOS EM CUIDADORES DE JOVENS ENTRE 18 E 24 ANOS COM TRANSTORNO DE HUMOR BIPOLAR E UNIPOLAR.” 2011. Web. 13 Dec 2019.

Vancouver:

ALVES GDGDS. SOBRECARGA E FATORES ASSOCIADOS EM CUIDADORES DE JOVENS ENTRE 18 E 24 ANOS COM TRANSTORNO DE HUMOR BIPOLAR E UNIPOLAR. [Internet] [Thesis]. Universidade Catolica de Pelotas; 2011. [cited 2019 Dec 13]. Available from: http://biblioteca.ucpel.tche.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=277.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

ALVES GDGDS. SOBRECARGA E FATORES ASSOCIADOS EM CUIDADORES DE JOVENS ENTRE 18 E 24 ANOS COM TRANSTORNO DE HUMOR BIPOLAR E UNIPOLAR. [Thesis]. Universidade Catolica de Pelotas; 2011. Available from: http://biblioteca.ucpel.tche.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=277

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

24. Hashimoto, Akiko; Matsuoka, Kiwamu; Yasuno, Fumihiko; Takahashi, Masato; Iida, Junzo; Jikumaru, Kiyoko. Frontal lobe function in elderly patients with Alzheimer's disease and caregiver burden. : アルツハイマー型認知症患者における前頭葉機能と介護負担の関係.

Degree: 博士(医学), 2017, Nara Medical University / 奈良県立医科大学

AIM: Understanding of the relationship between caregiver burden and the degree of behavioural deficits in patients with Alzheimer's disease (AD) is relatively limited. Therefore, it… (more)

Subjects/Keywords: Alzheimer's disease; caregiver burden; dementia; frontal lobe function

Page 1

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APA (6th Edition):

Hashimoto, Akiko; Matsuoka, Kiwamu; Yasuno, Fumihiko; Takahashi, Masato; Iida, Junzo; Jikumaru, K. (2017). Frontal lobe function in elderly patients with Alzheimer's disease and caregiver burden. : アルツハイマー型認知症患者における前頭葉機能と介護負担の関係. (Thesis). Nara Medical University / 奈良県立医科大学. Retrieved from http://hdl.handle.net/10564/3311

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hashimoto, Akiko; Matsuoka, Kiwamu; Yasuno, Fumihiko; Takahashi, Masato; Iida, Junzo; Jikumaru, Kiyoko. “Frontal lobe function in elderly patients with Alzheimer's disease and caregiver burden. : アルツハイマー型認知症患者における前頭葉機能と介護負担の関係.” 2017. Thesis, Nara Medical University / 奈良県立医科大学. Accessed December 13, 2019. http://hdl.handle.net/10564/3311.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hashimoto, Akiko; Matsuoka, Kiwamu; Yasuno, Fumihiko; Takahashi, Masato; Iida, Junzo; Jikumaru, Kiyoko. “Frontal lobe function in elderly patients with Alzheimer's disease and caregiver burden. : アルツハイマー型認知症患者における前頭葉機能と介護負担の関係.” 2017. Web. 13 Dec 2019.

Vancouver:

Hashimoto, Akiko; Matsuoka, Kiwamu; Yasuno, Fumihiko; Takahashi, Masato; Iida, Junzo; Jikumaru K. Frontal lobe function in elderly patients with Alzheimer's disease and caregiver burden. : アルツハイマー型認知症患者における前頭葉機能と介護負担の関係. [Internet] [Thesis]. Nara Medical University / 奈良県立医科大学; 2017. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/10564/3311.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hashimoto, Akiko; Matsuoka, Kiwamu; Yasuno, Fumihiko; Takahashi, Masato; Iida, Junzo; Jikumaru K. Frontal lobe function in elderly patients with Alzheimer's disease and caregiver burden. : アルツハイマー型認知症患者における前頭葉機能と介護負担の関係. [Thesis]. Nara Medical University / 奈良県立医科大学; 2017. Available from: http://hdl.handle.net/10564/3311

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


The Ohio State University

25. Stokes, Michele A. The Association of Adult Day Health Services Use and Burden, Self-Rated Health, and Additional Characteristics of Primary, Informal Caregivers of Older Adults.

Degree: PhD, Allied Medical Professions, 2011, The Ohio State University

 The objective of this research was to investigate characteristics, perceptions, and outcomes related to the use of adult day health services (ADS) among primary, informal… (more)

Subjects/Keywords: Gerontology; caregivers; older adults; adult day health services; caregiver burden

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APA (6th Edition):

Stokes, M. A. (2011). The Association of Adult Day Health Services Use and Burden, Self-Rated Health, and Additional Characteristics of Primary, Informal Caregivers of Older Adults. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1313610157

Chicago Manual of Style (16th Edition):

Stokes, Michele A. “The Association of Adult Day Health Services Use and Burden, Self-Rated Health, and Additional Characteristics of Primary, Informal Caregivers of Older Adults.” 2011. Doctoral Dissertation, The Ohio State University. Accessed December 13, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1313610157.

MLA Handbook (7th Edition):

Stokes, Michele A. “The Association of Adult Day Health Services Use and Burden, Self-Rated Health, and Additional Characteristics of Primary, Informal Caregivers of Older Adults.” 2011. Web. 13 Dec 2019.

Vancouver:

Stokes MA. The Association of Adult Day Health Services Use and Burden, Self-Rated Health, and Additional Characteristics of Primary, Informal Caregivers of Older Adults. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2019 Dec 13]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1313610157.

Council of Science Editors:

Stokes MA. The Association of Adult Day Health Services Use and Burden, Self-Rated Health, and Additional Characteristics of Primary, Informal Caregivers of Older Adults. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1313610157


Universiteit Utrecht

26. Beentjes, T.A.A. Nursing in different stages of a bipolar manic episode: Coping with dual loyalty and staying connected to outpatients and caregivers is easier when anticipated by having a good connection with both and making relapse prevention plans, a qualitative study.

Degree: 2013, Universiteit Utrecht

 Background: Bipolar disorder follows a pattern of different recurrent mood episodes. Acute mania causes marked impairment in social or occupational functioning and mania can be… (more)

Subjects/Keywords: Bipolar disorder; Dual Loyalty; Manic episodes; Caregiver burden

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APA (6th Edition):

Beentjes, T. A. A. (2013). Nursing in different stages of a bipolar manic episode: Coping with dual loyalty and staying connected to outpatients and caregivers is easier when anticipated by having a good connection with both and making relapse prevention plans, a qualitative study. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/262987

Chicago Manual of Style (16th Edition):

Beentjes, T A A. “Nursing in different stages of a bipolar manic episode: Coping with dual loyalty and staying connected to outpatients and caregivers is easier when anticipated by having a good connection with both and making relapse prevention plans, a qualitative study.” 2013. Masters Thesis, Universiteit Utrecht. Accessed December 13, 2019. http://dspace.library.uu.nl:8080/handle/1874/262987.

MLA Handbook (7th Edition):

Beentjes, T A A. “Nursing in different stages of a bipolar manic episode: Coping with dual loyalty and staying connected to outpatients and caregivers is easier when anticipated by having a good connection with both and making relapse prevention plans, a qualitative study.” 2013. Web. 13 Dec 2019.

Vancouver:

Beentjes TAA. Nursing in different stages of a bipolar manic episode: Coping with dual loyalty and staying connected to outpatients and caregivers is easier when anticipated by having a good connection with both and making relapse prevention plans, a qualitative study. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2019 Dec 13]. Available from: http://dspace.library.uu.nl:8080/handle/1874/262987.

Council of Science Editors:

Beentjes TAA. Nursing in different stages of a bipolar manic episode: Coping with dual loyalty and staying connected to outpatients and caregivers is easier when anticipated by having a good connection with both and making relapse prevention plans, a qualitative study. [Masters Thesis]. Universiteit Utrecht; 2013. Available from: http://dspace.library.uu.nl:8080/handle/1874/262987


California State University – San Bernardino

27. Torres, Janet Shin Yi. GENDER DIFFERENCES IN CAREGIVER BURDEN AMONG ALZHEIMER'S PATIENTS.

Degree: MSW, School of Social Work, 2018, California State University – San Bernardino

  The purpose of this research was to explore the gender differences in caregiver burden in Alzheimer’s patients in the Inland Empire. Currently, there are… (more)

Subjects/Keywords: gender differences; Alzheimer's disease; caregiver burden; Social Work

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Torres, J. S. Y. (2018). GENDER DIFFERENCES IN CAREGIVER BURDEN AMONG ALZHEIMER'S PATIENTS. (Thesis). California State University – San Bernardino. Retrieved from http://scholarworks.lib.csusb.edu/etd/681

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Torres, Janet Shin Yi. “GENDER DIFFERENCES IN CAREGIVER BURDEN AMONG ALZHEIMER'S PATIENTS.” 2018. Thesis, California State University – San Bernardino. Accessed December 13, 2019. http://scholarworks.lib.csusb.edu/etd/681.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Torres, Janet Shin Yi. “GENDER DIFFERENCES IN CAREGIVER BURDEN AMONG ALZHEIMER'S PATIENTS.” 2018. Web. 13 Dec 2019.

Vancouver:

Torres JSY. GENDER DIFFERENCES IN CAREGIVER BURDEN AMONG ALZHEIMER'S PATIENTS. [Internet] [Thesis]. California State University – San Bernardino; 2018. [cited 2019 Dec 13]. Available from: http://scholarworks.lib.csusb.edu/etd/681.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Torres JSY. GENDER DIFFERENCES IN CAREGIVER BURDEN AMONG ALZHEIMER'S PATIENTS. [Thesis]. California State University – San Bernardino; 2018. Available from: http://scholarworks.lib.csusb.edu/etd/681

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

28. Griffiths, Alys Wyn. The predictive value of psychological defeat and entrapment.

Degree: PhD, 2015, University of Manchester

 This thesis investigated the longitudinal role of defeat and entrapment in populations where these factors were expected to be particularly relevant (a sample of individuals… (more)

Subjects/Keywords: 616.001; defeat; entrapment; depression; anxiety; caregiver burden; psychometric

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APA (6th Edition):

Griffiths, A. W. (2015). The predictive value of psychological defeat and entrapment. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-predictive-value-of-psychological-defeat-and-entrapment(87be8ba9-3e95-419d-84dd-953228403ff6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644479

Chicago Manual of Style (16th Edition):

Griffiths, Alys Wyn. “The predictive value of psychological defeat and entrapment.” 2015. Doctoral Dissertation, University of Manchester. Accessed December 13, 2019. https://www.research.manchester.ac.uk/portal/en/theses/the-predictive-value-of-psychological-defeat-and-entrapment(87be8ba9-3e95-419d-84dd-953228403ff6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644479.

MLA Handbook (7th Edition):

Griffiths, Alys Wyn. “The predictive value of psychological defeat and entrapment.” 2015. Web. 13 Dec 2019.

Vancouver:

Griffiths AW. The predictive value of psychological defeat and entrapment. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Dec 13]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-predictive-value-of-psychological-defeat-and-entrapment(87be8ba9-3e95-419d-84dd-953228403ff6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644479.

Council of Science Editors:

Griffiths AW. The predictive value of psychological defeat and entrapment. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-predictive-value-of-psychological-defeat-and-entrapment(87be8ba9-3e95-419d-84dd-953228403ff6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644479


Louisiana State University

29. Jordan, Rhonda Lee. The effects of coping strategies on burden among Louisiana Alzheimer's disease caregivers.

Degree: MSW, Social Work, 2012, Louisiana State University

 The purpose of this study was to examine the relationship between three coping strategies—emotion-focused, task-focused, and avoidance-focused—and the perceived burden among Louisiana Alzheimer’s disease caregivers.… (more)

Subjects/Keywords: Alzheimer's disease; caregiver; social work; burden; coping strategies; coping

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Jordan, R. L. (2012). The effects of coping strategies on burden among Louisiana Alzheimer's disease caregivers. (Masters Thesis). Louisiana State University. Retrieved from etd-04192012-135431 ; https://digitalcommons.lsu.edu/gradschool_theses/707

Chicago Manual of Style (16th Edition):

Jordan, Rhonda Lee. “The effects of coping strategies on burden among Louisiana Alzheimer's disease caregivers.” 2012. Masters Thesis, Louisiana State University. Accessed December 13, 2019. etd-04192012-135431 ; https://digitalcommons.lsu.edu/gradschool_theses/707.

MLA Handbook (7th Edition):

Jordan, Rhonda Lee. “The effects of coping strategies on burden among Louisiana Alzheimer's disease caregivers.” 2012. Web. 13 Dec 2019.

Vancouver:

Jordan RL. The effects of coping strategies on burden among Louisiana Alzheimer's disease caregivers. [Internet] [Masters thesis]. Louisiana State University; 2012. [cited 2019 Dec 13]. Available from: etd-04192012-135431 ; https://digitalcommons.lsu.edu/gradschool_theses/707.

Council of Science Editors:

Jordan RL. The effects of coping strategies on burden among Louisiana Alzheimer's disease caregivers. [Masters Thesis]. Louisiana State University; 2012. Available from: etd-04192012-135431 ; https://digitalcommons.lsu.edu/gradschool_theses/707


UCLA

30. Saria, Marlon Garzo. The Hidden Morbidity of Cancer: An Exploratory Study of Burden in Caregivers of Cancer Patients with Brain Metastases.

Degree: Nursing, 2016, UCLA

 Caregiving is a highly individualized experience. While numerous papers have been published on caregiver burden in the context of a variety of diagnoses and conditions,… (more)

Subjects/Keywords: Nursing; Brain Metastases; Cancer Caregiving; Caregiver Burden; Cognitive Impairment; Coping

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Saria, M. G. (2016). The Hidden Morbidity of Cancer: An Exploratory Study of Burden in Caregivers of Cancer Patients with Brain Metastases. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/9nt2m1hh

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Saria, Marlon Garzo. “The Hidden Morbidity of Cancer: An Exploratory Study of Burden in Caregivers of Cancer Patients with Brain Metastases.” 2016. Thesis, UCLA. Accessed December 13, 2019. http://www.escholarship.org/uc/item/9nt2m1hh.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Saria, Marlon Garzo. “The Hidden Morbidity of Cancer: An Exploratory Study of Burden in Caregivers of Cancer Patients with Brain Metastases.” 2016. Web. 13 Dec 2019.

Vancouver:

Saria MG. The Hidden Morbidity of Cancer: An Exploratory Study of Burden in Caregivers of Cancer Patients with Brain Metastases. [Internet] [Thesis]. UCLA; 2016. [cited 2019 Dec 13]. Available from: http://www.escholarship.org/uc/item/9nt2m1hh.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Saria MG. The Hidden Morbidity of Cancer: An Exploratory Study of Burden in Caregivers of Cancer Patients with Brain Metastases. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/9nt2m1hh

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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