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Books on the topic 'Parent psychological distress'

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Author: Grafiati
Published: 10 December 2022
Last updated: 28 January 2023

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1

Barnett, Rosalind C. Adult son-parent relationships and their associations with sons' psychological distress. Wellesley, MA: Wellesley College, Center for Research on Women, 1991.

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2

Barnett, Rosalind C. Adult son-parent relationships and their associations with sons' psychological distress. Wellesley, MA: Wellesley College, Center for Research on Women, 1991.

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3

Barnett, Rosalind C. Adult son-parent relationships and their associations with sons' psychological distress. Wellesley, Mass: Wellesley College, 1991.

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4

Barnett, Rosalind C. Gender, parent-role quality and psychological distress: A study of men and women in dual-earner couples. Wellesley, MA: Wellesley College, Center for Research on women, 1992.

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5

Barnett, Rosalind C. Gender, parent-role quality and psychological distress: A study of men and women in dual-earner couples. Wellesley, MA: Wellesley College, Center for Research on women, 1992.

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6

Barnett, Rosalind C. Gender, parent-role quality and psychological distress: A study of men and women in dual-earner couples. Wellesley, Mass: Wellesley College, 1992.

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7

Hope, Tana Louise. Treatment outcome of childhood obesity: The effect of children's psychological distress and problematic behavior. [s.l.]: Louisiana State University, 2001.

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8

Prell, Jan R. Psychological distress and social support in child abusive parents. 1989.

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9

Shaw, Richard J., and Sarah Horwitz. Treatment of Psychological Distress in Parents of Premature Infants: PTSD in the NICU. American Psychiatric Association Publishing, 2020.

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10

Shaw, Richard J., and Sarah Horwitz. Treatment of Psychological Distress in Parents of Premature Infants: PTSD in the NICU. American Psychiatric Association Publishing, 2020.

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11

Saadat, Haleh, and Zeev N. Kain. Psychological Preparation of the Pediatric Patient for Surgery. Edited by Kirk Lalwani, Ira Todd Cohen, Ellen Y. Choi, and Vidya T. Raman. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190685157.003.0057.

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Each year, about six million children undergo surgical procedures in the United States. More than 80% of all pediatric procedures in the United States are on an outpatient basis without hospital preoperative or postoperative admission. More than 60% of these children manifest emotional distress prior to the procedures and at the induction of anesthesia. The intense distress may lead to negative postoperative physiological and psychological outcomes in children and affect parental satisfaction. Preoperative stress can also exaggerate negative memories, which can exaggerate distress at subsequent procedures. Studies have looked into the incorporation of pharmacological agents as well as nonpharmacological strategies such as parental presence, and behavioral techniques such as imagery, relaxation, and hypnosis in the management of preoperative anxiety. The goal of this chapter is to examine the effects of preoperative anxiety and the effectiveness of these strategies in preventing preoperative psychological stress in children.
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12

Lawrence, Erika, and Kieran T. Sullivan, eds. The Oxford Handbook of Relationship Science and Couple Interventions. Oxford University Press, 2014. http://dx.doi.org/10.1093/oxfordhb/9780199783267.001.0001.

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Marriage and other long-term committed relationships are an integral part of our lives and confer many benefits. Unfortunately, many couples experience significant relationship distress and about half of marriages end in divorce. Among those who stay married, a notable number of couples remain in stably, severely distressed marriages for years or even decades. Given the serious physical and psychological consequences of relationship distress and divorce for spouses and their children, it is clear that relationship science––the basic and applied study of relationship development, maintenance, and dysfunction––is of critical importance.The Oxford Handbook of Relationship Science and Couple Interventionsshowcases cutting-edge research in relationship science, including couple functioning, relationship education, and couple therapy. The book begins with the most current definitions of and classifications for relationship dysfunction, which are reflected in the most recent versions of theDiagnostic and Statistical Manual of Mental Disorder (DSM-5)and theInternational Classification of Diagnoses (ICD-11). Next, the latest research on the biological, psychological, and interpersonal causes and correlates of couple dysfunction and subsequent treatment implications is presented. The latest findings regarding empirically supported prevention and treatment interventions for couple dysfunction are then presented, and diversity and cultural issues are discussed in the context of working with couples. The information contained in this handbook will benefit researchers who seek to understand relationship distress and design interventions to prevent and treat couple distress, and clinicians who are diagnosing, assessing, and treating couple dysfunction in their practices.
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13

Emanuel, Linda L., Richard A. Powell, George Handzo, Kelly Nichole Michelson, and Lara Dhingra. Validated assessment tools for psychological, spiritual, and family issues. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0074.

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Palliative care has a foundational commitment to integrate attention to psychological, spiritual, and family issues with biomedical matters. This requires being able to measure them. A limited number of assessment tools have been subjected to validity studies. Many measures are for service assessment, including assessments made as part of quality improvement; but a range of rigorously developed measures, including patient-reported outcome measures, is available. Those that are multidimensional and feasible in the real world of patient care are fewer. Domain-specific screening and measurement tools that focus on depression, anxiety, and a more generalized state of psychological distress as well as spirituality are described. Additional tools for measuring delirium and adjustment disorders or grief and bereavement are referenced. While rigorous, comprehensive family assessments and measures are not available, multiple measures that focus on particular aspects of family need and function are described.
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14

Okazaki, Sumie, and Nancy Abelmann. Korean American Families in Immigrant America. NYU Press, 2018. http://dx.doi.org/10.18574/nyu/9781479804207.001.0001.

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This book about Korean American immigrant families is the result of a collaboration between an anthropologist and a psychologist. Combining quantitative surveys with family ethnography, the book explored the central question, How do Korean American teens and parents navigate immigrant America? Both survey and ethnographic data revealed that acculturation differences between parents and teens—long assumed in the psychological literature to account for distress—did not necessarily make for family hardship. Instead, this research found that families struggle together, although not always easily, to figure out how best to navigate an American society that they all understood to be racist. This is not to say that the parents did not speak about cultural distinctions or that they were unconcerned about academic achievement. But what these parents anguished over most was how to fortify their children with protective psychological health and character traits that would allow them to succeed. Ethnographic chapters on five Korean American immigrant families introduce the parenting strategies and adolescents’ responses, which were at times defiantly resistant, sometimes accommodating, and at other times enormously appreciative. The book examines the delicate negotiations between parents and teens in the intimacy of family life, following them from homes to shopping malls, music recitals, church, workplaces, and school. The five families reflect a diversity of family dynamics, but uniting them all is the hard work that parents and children engage in to maintain the bonds of their family relationships.
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15

Mandeville, Anna L. Non-pharmacological methods of acute pain management. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199234721.003.0003.

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Psychological factors are a key part of pain perception as articulated in the neuromatrix model of pain. Psychoeducational interventions are of significant value in acute pain management and have reduced pain severity, distress, and length of hospital stay. Mood, beliefs about pain and illness, previous experience of pain, and the behaviour of health care professionals all influence pain perception and response to pain. Helping patients reappraise the threat value of pain through tailored information giving and where needed cognitive behavioural interventions are practical strategies. Attention control methods, including clinical hypnosis, are effective in reducing procedural pain.
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16

Grassi, Luigi, Maria Giulia Nanni, and Rosangela Caruso. Psychotherapeutic interventions. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198806677.003.0010.

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Psychotherapy is an integrative and integrated part of modern patient/relation-centered care in the advanced and terminal phases of physical illness. Psychiatric disorders (e.g. depressive spectrum, stress-related, and anxiety disorders), other clinically significant psychosocial conditions (e.g. demoralization, existential pain) and interpersonal, psychological, and spiritual needs have to be addressed by psychological intervention. Supportive-Expressive Group Psychotherapy (SEGT), Meaning-Centered Psychotherapy (MCT), Managing Cancer and Living Meaningfully Therapy (CALM), cognitive-existential therapy, dignity therapy (DT) and other psychotherapeutic interventions have been developed over the last 40 years. These treatments have proved to be effective in increasing the patients’ sense of dignity, purpose, and meaning, and to reduce demoralization, anxiety, and existential distress at the end of life. Also Family Focused Grief Therapy (FFGT) and grief therapy have shown to be effective in overcoming anxiety, depression, and complicated grief symptoms both before and after loss. Psychotherapy should thus be considered a mandatory ingredient of palliative care.
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17

Kissane, David W., and Talia I. Zaider. Bereavement. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0177.

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The phenomena and trajectory of mourning as a normal adaptive process are differentiated from clinical depression, avoidant and complicated grief, post-traumatic distress disorder, and other forms of pathological grief. Anticipatory grief can be a particular challenge during palliative care. The family is recognized as the major source of social support and the environment in which grief is shared with others. Key risk factors for pathological bereavement outcomes can be identified on admission to palliative care, permitting preventive models of psychological care to be used through palliative care into bereavement. Models of therapy include supportive-expressive, interpersonal, cognitive behavioural, family focused, and specific therapy for complicated grief. Pharmacotherapy can judiciously accompany psychotherapy. Life-cycle issues include bereaved children, siblings, parents, and grief for the very elderly. Grief can be stigmatized and ambiguous in special circumstances, yet positive growth is a desirable outcome from any loss.
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18

Palmieri, Arianna, Francesco Pagnini, and Chris Gibbons. Complementary and alternative medicines and ALS. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198757726.003.0005.

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Complementary and alternative medicines (CAMs) are medical practices and products that are not part of conventional medical practice, including drugs, diets, mind–body approaches, herbs, and exercises. Given the lack of conventional treatments, it is worth exploring alternative medicines, with the aim of improving the general well-being of the person with ALS. CAMs should be approached with an open attitude by the physicians, who can recognize the potential not only for the treatment itself, but also for re-establishing a sort of perceived control. Some of these treatments have provided interesting results. In particular, the uses of hypnosis and meditation have been explored more rigorously. Both approaches lead to an improvement of well-being and a reduction of psychological distress.
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19

Sullivan, Kieran T., and Erika Lawrence. Introduction. Edited by Erika Lawrence and Kieran T. Sullivan. Oxford University Press, 2016. http://dx.doi.org/10.1093/oxfordhb/9780199783267.013.19.

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Long-term committed intimate relationships such as marriage are an integral part of our lives and confer many benefits but many couples experience significant relationship distress and about half of all marriages end in divorce. The purpose of this edited volume is to showcase cutting-edge research on couple functioning and interventions, including the development of new guidelines for determining whether a given couple therapy is empirically supported, the relation between couple functioning and individual physical and psychological functioning (e.g., chronic pain, depression, anxiety), the role of genetics in interpersonal processes, best practices for the assessment, prevention, and treatment of couple dysfunction, and the relevance of couple functioning and couple therapy to the structure and utility of classification systems such as theDiagnostic and Statistical Manual of Mental Disorders (DSM) and the International Classification of Diseases (ICD).
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20

Makurumidze, Getrude, Anna Gamell, and Emili Letang. AIDS Orphans and Other Children Affected by HIV. Edited by Mary Ann Cohen, Jack M. Gorman, Jeffrey M. Jacobson, Paul Volberding, and Scott Letendre. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199392742.003.0005.

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Since the beginning of the HIV/AIDS epidemic, the number of deaths in reproductive age groups has led to nearly 18 million children being left orphaned. Orphans are not only faced with the loss of one or both parents but may also suffer loss of property and inheritance, disruption from school, and psychosocial distress from the stigma associated with HIV/AIDS. This chapter explores the psychological, social, and cultural aspects of HIV/AIDS orphanhood. It addresses the financial and emotional support that orphans and their caregivers need, as well as key strategies shown to be effective to protect, support, and empower orphans and vulnerable children (OVC). Such strategies include providing education, psychosocial care and support, household economic strengthening, social protection, health and nutrition, child and legal protection, and capacity building. However, despite the considerable progress achieved, multiple challenges still prevent many OVC from receiving effective care and support. These aspects need to be urgently addressed in order to build evidence-based programs, respond to the needs of all AIDS-affected children, and achieve the dream of an AIDS-free generation.
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21

McGuire, James, and Lisa Wootton. Multiple agencies with diverse goals. Edited by Alec Buchanan and Lisa Wootton. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198738664.003.0015.

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This chapter charts the relationships between three large areas of background knowledge and professional practice, at the intersection of which everyday work in forensic mental health takes place. We describe the three underpinning models (biomedical, psychological, and sociological) the differences between them in training and in outlook, and the relationship of each to the legal context in which all must operate. Representing different models of human problems and distress, we recognize that sometimes there is friction between them. Their diverse perspectives notwithstanding, these models can be integrated, and they all have an indispensable part to play in how we understand and respond to the difficulties of working with people with mental health problems who also break the law. We illustrate this with reference to how services are delivered, and conclude by discussing the role played by Multi- Agency Public Protection Arrangements (MAPPA) in England and Wales.
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22

Barr, Jane Ellen. Stoma therapy in palliative care. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0412.

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Patients with ostomies, wounds, or incontinence in the setting of a serious or life-threatening illness experience numerous challenges, including distress related to pain and other symptoms, psychological disturbances, and family concerns. Expert management of these conditions and their many complications is an essential part of a comprehensive palliative plan of care. In many countries, nurse specialists with advanced training in the management of ostomies, wounds, or incontinence are available as consultants or as members of a specialist palliative care team. These professionals can improve health care and quality of life for selected patients across venues of care that include hospital, home, long-term care, hospice, and specialized settings. If a stoma nurse specialist is available, he or she may have a key role in directing decision-making and care management related to these problems, evaluating and controlling symptoms that cause patients and families suffering, and providing psychosocial and spiritual support.
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23

Freudenberg, Nicholas. At What Cost. Oxford University Press, 2021. http://dx.doi.org/10.1093/oso/9780190078621.001.0001.

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Every day people decide what to eat, how to educate their children, where to find health care, and how to connect to others. For many, freely choosing a lifestyle defines the American dream. But in the 21st century, these choices are increasingly constructed by corporations and designed not to promote well-being, happiness, and planetary health, but to increase corporate profits and power. As a result, the decisions that corporations encourage individuals to make can lead to premature death, illness, or psychological distress as well as environmental pollution and social conflict. At What Cost: Modern Capitalism and the Future of Health maps the landscape of the changing role of capitalism in shaping health in America, documenting the human costs of the dominant political and economic system. It describes how globalization, financial speculation, monopoly concentration, and business control of science and technology have enhanced the ability of corporations and their allies to overwhelm influences of government, family, and community. It analyses how 21st-century capitalism structures the choices that affect the well-being of individuals, families, communities, and the planet. The book also explores how people, governments, civil society, and social movements are challenging corporate domination and forging alternative paths to a healthier, more sustainable world. While other books have explored pieces of this story, At What Cost offers a comprehensive analysis of the health consequences of modern capitalism. It provides citizens, parents, activists, scholars, and policy makers with the evidence they need to construct a better world for current and future generations.
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