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Noriko Yamamoto-Mitani

Biographic Data

ID3886256
NAMENoriko Yamamoto-Mitani
GIVEN NAMESNoriko
FAMILY NAMEYamamoto-Mitani
SIGNATUREYAMAMOTO-MITANI N
AFFILIATIONSNoriko Yamamoto-Mitani is Associate Professor of Visiting Nursing at Chiba University School of Nursing, Japan. Previously she was a Visiting Professor at the University of California, Los Angeles. Her research interests include assisting families of older adults with dementia, quality of life of older adults with dementia, and quality assurance for home health care nursing
VERIFIEDNo
TOTAL WORKS9
TOTAL CITATIONS15
AUTHOR COUNT9
EDITOR COUNT0
FIRST PUBLICATION YEAR2002
LATEST PUBLICATION YEAR2021
H-INDEX2
  • Infant Injury Prevention Education for Pregnant Women Attending Antenatal Class: A Quasi-Experimental Study

    Open Access•Chikako Honda, Takashi Naruse et al.•ARTICLE•International Journal of…•2021

    It is important to educate caregivers in order to prevent infant injuries. However, there have been few studies on the effects of education on pregnant women. This study aimed to evaluate the effects of injury prevention group education on this group. Study participants were recruited from a group of pregnant mothers attending an antenatal class in Tokyo. Participants were assigned to either the intervention or control group based on the month in…

  • The Experience of Persons With Hematological Malignancy When Communicating With Health Care Professionals

    Open Access•Fumika Horinuki, Maiko Noguchi-Watanabe et al.•ARTICLE•Qualitative Health Research•2018•References: 44

    This study aimed to elucidate the experiences of Japanese persons with hematological malignancy (PHMs) in communicating with health care professionals (HCPs), from diagnosis to the end of life, as recalled by their families. We interviewed 14 bereaved families and analyzed the data using the basic techniques of grounded theory. We found that PHMs lived to the fullest possible when they experienced ownership of their illness process despite their …

  • Regaining my new life: Daily lives of suicide-bereaved individuals

    Mami Kasahara-Kiritani, Mari Ikeda et al.•ARTICLE•Death Studies•2017•Cited by: 2•References: 1

    This study aimed to develop a conceptual framework of the experience of persons who have lost a family member to suicide in Japan. The authors conducted in-depth interviews with 24 such family members. They conceptualized their experience as a process of regaining my new life. Initially, their lives were out of their hands, but gradually they learned striving skills and recuperative conditioning, and integrated the skills to regain their lives. S…

  • Female family caregivers face a higher risk of hypertension and lowered estimated glomerular filtration rates: A cross-sectional, comparative study

    Open Access•Yasuko Torimoto‐Sasai, Yasuko Torimoto-Sasai et al.•ARTICLE•BMC Public Health•2015

    Results suggest that female caregivers are at a higher risk of conditions such as cerebral, cardiovascular or kidney diseases than non-caregivers. Steps must be taken to identify caregivers with high blood pressure and lowered eGFR and provide them with the support they need before these risk factors develop into serious diseases

  • Home Care Nurses' Provision of Support to Families of the Elderly at the End of Life

    Open Access•Yuko Hirano, Noriko Yamamoto-Mitani et al.•ARTICLE•Qualitative Health Research•2011•Cited by: 1•References: 12

    In this article we describe our study of assistance for family decisions and caregiving by Japanese home care nurses to families of elderly relatives at the end of life. The participants were 31 nurses who had been evaluated as providing good end-of-life care. We carried out semistructured interviews concerning the practice of family support in two cases (cancer and noncancer). We conducted a qualitative analysis using the constant comparative ap…

  • The Meaning of Family Caregiving in Japan and the United States: A Qualitative Comparative Study

    Open Access•M Wallhagen, Margaret I Wallhagen et al.•ARTICLE•Journal of Transcultural Nursing•2006

    This study explores how cultural values affect the meaning and experiences of daughter (or daughter-in-law) caregivers of elderly persons with dementia by comparing caregivers in the United States and Japan. Nine American and seven Japanese caregivers were interviewed twice at 6-month intervals. Interviews were audiotaped and analyzed using constant-comparative techniques. Data suggest that moral obligation to care and intense loss are two univer…

  • Subjective quality of life and positive appraisal of care among Japanese family caregivers of older adults

    Open Access•Noriko Yamamoto-Mitani, Noriko Yamamoto‐mitani et al.•ARTICLE•Quality of Life Research•2004

  • When Caregiving Ends: The Course of Depressive Symptoms After Bereavement

    Open Access•Carol S Aneshensel, Amanda L Botticello et al.•ARTICLE•Journal of Health and Social…•2004•Cited by: 12•References: 33

    This study describes depressive symptoms among caregivers following bereavement and connects these trajectories to earlier features of caregiving using life course and stress process theory. Data are from a six-wave longitudinal survey (five years) of spouses and adult children caring for someone with Alzheimer's Disease. The analytic subsample (N = 291) is defined by death of the care-recipient after the baseline interview. A latent class mixtur…

  • Pursuit of Psychological Well-Being (Ikigai) and the Evolution of Self-Understanding in the Context of Caregiving in Japan

    Open Access•Noriko Yamamoto-Mitani, Noriko Yamamoto‐mitani et al.•ARTICLE•Culture Medicine and Psychiatry•2002

    Using the Japanese concept of ikigai, which describes a certain state of psychological well-being, this study explores how Japanese family caregivers of elderly parents with dementia pursue, maintain, or attempt to regain their psychological well-being in the face of the hardship of caregiving. Using constant comparative methodology, twenty-six Japanese women who were caring for an elderly demented parent or parent-in-law were interviewed. Based …

  • When Caregiving Ends: The Course of Depressive Symptoms After Bereavement

    Open Access•Carol S Aneshensel, Amanda L Botticello et al.•ARTICLE•Journal of Health and Social…•2004•Cited by: 12•References: 33

    This study describes depressive symptoms among caregivers following bereavement and connects these trajectories to earlier features of caregiving using life course and stress process theory. Data are from a six-wave longitudinal survey (five years) of spouses and adult children caring for someone with Alzheimer's Disease. The analytic subsample (N = 291) is defined by death of the care-recipient after the baseline interview. A latent class mixtur…

  • Regaining my new life: Daily lives of suicide-bereaved individuals

    Mami Kasahara-Kiritani, Mari Ikeda et al.•ARTICLE•Death Studies•2017•Cited by: 2•References: 1

    This study aimed to develop a conceptual framework of the experience of persons who have lost a family member to suicide in Japan. The authors conducted in-depth interviews with 24 such family members. They conceptualized their experience as a process of regaining my new life. Initially, their lives were out of their hands, but gradually they learned striving skills and recuperative conditioning, and integrated the skills to regain their lives. S…

  • Home Care Nurses' Provision of Support to Families of the Elderly at the End of Life

    Open Access•Yuko Hirano, Noriko Yamamoto-Mitani et al.•ARTICLE•Qualitative Health Research•2011•Cited by: 1•References: 12

    In this article we describe our study of assistance for family decisions and caregiving by Japanese home care nurses to families of elderly relatives at the end of life. The participants were 31 nurses who had been evaluated as providing good end-of-life care. We carried out semistructured interviews concerning the practice of family support in two cases (cancer and noncancer). We conducted a qualitative analysis using the constant comparative ap…

  • Pursuit of Psychological Well-Being (Ikigai) and the Evolution of Self-Understanding in the Context of Caregiving in Japan

    Open Access•Noriko Yamamoto-Mitani, Noriko Yamamoto‐mitani et al.•ARTICLE•Culture Medicine and Psychiatry•2002

    Using the Japanese concept of ikigai, which describes a certain state of psychological well-being, this study explores how Japanese family caregivers of elderly parents with dementia pursue, maintain, or attempt to regain their psychological well-being in the face of the hardship of caregiving. Using constant comparative methodology, twenty-six Japanese women who were caring for an elderly demented parent or parent-in-law were interviewed. Based …

  • Subjective quality of life and positive appraisal of care among Japanese family caregivers of older adults

    Open Access•Noriko Yamamoto-Mitani, Noriko Yamamoto‐mitani et al.•ARTICLE•Quality of Life Research•2004

  • When Caregiving Ends: The Course of Depressive Symptoms After Bereavement

    Open Access•Carol S Aneshensel, Amanda L Botticello et al.•ARTICLE•Journal of Health and Social…•2004•Cited by: 12•References: 33

    This study describes depressive symptoms among caregivers following bereavement and connects these trajectories to earlier features of caregiving using life course and stress process theory. Data are from a six-wave longitudinal survey (five years) of spouses and adult children caring for someone with Alzheimer's Disease. The analytic subsample (N = 291) is defined by death of the care-recipient after the baseline interview. A latent class mixtur…

  • The Meaning of Family Caregiving in Japan and the United States: A Qualitative Comparative Study

    Open Access•M Wallhagen, Margaret I Wallhagen et al.•ARTICLE•Journal of Transcultural Nursing•2006

    This study explores how cultural values affect the meaning and experiences of daughter (or daughter-in-law) caregivers of elderly persons with dementia by comparing caregivers in the United States and Japan. Nine American and seven Japanese caregivers were interviewed twice at 6-month intervals. Interviews were audiotaped and analyzed using constant-comparative techniques. Data suggest that moral obligation to care and intense loss are two univer…

  • Home Care Nurses' Provision of Support to Families of the Elderly at the End of Life

    Open Access•Yuko Hirano, Noriko Yamamoto-Mitani et al.•ARTICLE•Qualitative Health Research•2011•Cited by: 1•References: 12

    In this article we describe our study of assistance for family decisions and caregiving by Japanese home care nurses to families of elderly relatives at the end of life. The participants were 31 nurses who had been evaluated as providing good end-of-life care. We carried out semistructured interviews concerning the practice of family support in two cases (cancer and noncancer). We conducted a qualitative analysis using the constant comparative ap…

  • Female family caregivers face a higher risk of hypertension and lowered estimated glomerular filtration rates: A cross-sectional, comparative study

    Open Access•Yasuko Torimoto‐Sasai, Yasuko Torimoto-Sasai et al.•ARTICLE•BMC Public Health•2015

    Results suggest that female caregivers are at a higher risk of conditions such as cerebral, cardiovascular or kidney diseases than non-caregivers. Steps must be taken to identify caregivers with high blood pressure and lowered eGFR and provide them with the support they need before these risk factors develop into serious diseases

  • Regaining my new life: Daily lives of suicide-bereaved individuals

    Mami Kasahara-Kiritani, Mari Ikeda et al.•ARTICLE•Death Studies•2017•Cited by: 2•References: 1

    This study aimed to develop a conceptual framework of the experience of persons who have lost a family member to suicide in Japan. The authors conducted in-depth interviews with 24 such family members. They conceptualized their experience as a process of regaining my new life. Initially, their lives were out of their hands, but gradually they learned striving skills and recuperative conditioning, and integrated the skills to regain their lives. S…

  • The Experience of Persons With Hematological Malignancy When Communicating With Health Care Professionals

    Open Access•Fumika Horinuki, Maiko Noguchi-Watanabe et al.•ARTICLE•Qualitative Health Research•2018•References: 44

    This study aimed to elucidate the experiences of Japanese persons with hematological malignancy (PHMs) in communicating with health care professionals (HCPs), from diagnosis to the end of life, as recalled by their families. We interviewed 14 bereaved families and analyzed the data using the basic techniques of grounded theory. We found that PHMs lived to the fullest possible when they experienced ownership of their illness process despite their …

  • Infant Injury Prevention Education for Pregnant Women Attending Antenatal Class: A Quasi-Experimental Study

    Open Access•Chikako Honda, Takashi Naruse et al.•ARTICLE•International Journal of…•2021

    It is important to educate caregivers in order to prevent infant injuries. However, there have been few studies on the effects of education on pregnant women. This study aimed to evaluate the effects of injury prevention group education on this group. Study participants were recruited from a group of pregnant mothers attending an antenatal class in Tokyo. Participants were assigned to either the intervention or control group based on the month in…

Medicine (8 works) · Psychology (6 works) · Family medicine (4 works) · Nursing (4 works) · Developmental psychology (3 works) · Family caregivers (3 works) · Gerontology (3 works) · Grief, Bereavement, and Mental Health (3 works) · Intergenerational Family Dynamics and Caregiving (3 works) · Public health (3 works)

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