Relevant bibliographies by topics / Psychosocial experiences of cancer

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Psychosocial experiences of cancer'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Psychosocial experiences of cancer.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Psychosocial experiences of cancer"

1

Wenger, Lisa M., John L. Oliffe, and Joan L. Bottorff. "Psychosocial Oncology Supports for Men." American Journal of Men's Health 10, no. 1 (November 11, 2014): 39–58. http://dx.doi.org/10.1177/1557988314555361.

Full text
Abstract:
Although men’s cancer experiences have received limited attention within the field of psychosocial oncology, increasing attention is being devoted to the development and evaluation of men-centered programs. This scoping review describes this emergent body of literature, detailing the focus, participation, and impact of interventions designed to help men with cancer build illness-specific knowledge, adapt to illness, manage side effects, distress, and uncertainty, sustain relationships, and more. Striving to build on existing knowledge, research gaps and opportunities are discussed, including a need for stronger methodologies, more tailored and targeted supports, attention to the experiences of men with nonprostate cancers, and the explicit integration of gender analyses in the research process.
APA, Harvard, Vancouver, ISO, and other styles
2

Feraco, Angela Marie, Sarah R. McCarthy, P. Jeet Das, Anna Revette, James A. Tulsky, and Joanne Wolfe. "Pediatric cancer care professionals’ experiences with an interprofessional communication intervention." Journal of Clinical Oncology 36, no. 34_suppl (December 1, 2018): 53. http://dx.doi.org/10.1200/jco.2018.36.34_suppl.53.

Full text
Abstract:
53 Background: The National Academy of Medicine recommends interprofessional collaboration to promote optimal patient- and family-centered care. We sought to understand whether medical and psychosocial professionals who participated in an interprofessional communication intervention perceived it as distinct from usual clinical care. Methods: Our intervention targeted “medical” (physicians, nurse practitioners) and “psychosocial” (social workers, psychologists) professionals. It consisted of an interprofessional family conference, using a structured conversation guide, conducted during the first 6 months of a child’s cancer care. Conferences aimed to enable families to share hopes and worries and ask questions about their child’s care. Clinicians received a 60-minute training focused on communication skills, such as eliciting families’ hopes and worries, and suggested approaches to collaborating during conferences. Clinicians participated in debriefing interviews after each conference (range 1-3). Three of us conducted thematic analysis of interview data. Results: Twenty-two professionals (6 attending MDs, 4 fellow MDs, 8 NPs, and 8 psychosocial clinicians) gave 34 interviews. Medical and psychosocial professionals described interprofessional family conferences as distinct from usual practice patterns, largely due to their interprofessional colleagues’ presence. This co-presence contributed to “being on the same page.” Conferences sometimes bred a new understanding of a family’s needs and consequent care changes. However, both medical and psychosocial professionals noted that psychosocial professionals often were not vocal contributors to the conference. Some psychosocial clinicians reported being unsure of “the rules.” Conclusions: An interprofessional communication intervention promoted shared understanding between interprofessional colleagues. However, medical professionals were described as more vocal, perhaps due to insufficient role clarity or medical dominance.
APA, Harvard, Vancouver, ISO, and other styles
3

Fernandez, A. S. "Exploring the Post-Treatment Experiences of Childhood Cancer Survivors." Journal of Global Oncology 4, Supplement 2 (October 1, 2018): 119s. http://dx.doi.org/10.1200/jgo.18.44700.

Full text
Abstract:
Background: One of the great successes in medicine is the treatment of childhood cancer. Due to the overall increase in the survival rate of individuals with cancer, the disease is now considered a chronic condition (Meeske, Patel, Palmer, Nelson, & Parow, 2007) rather than a terminal illness, drawing tremendous amount of attention toward examining the subjective well-being among cancer patients and survivors. In the Philippines, there is a growing number of childhood cancer survivors, however, they face posttreatment challenges that are given less attention in research in the country. Aim: The study sought to understand the experiences of Filipino childhood cancer survivors, focusing on the challenges, triumphs, and experiences related to postcancer treatment. An awareness and a better understanding of these will likely help psychosocial oncology professionals improve survivors´ level of functioning and quality of life in the posttreatment period. Methods: Using a qualitative design, six focus group discussions were conducted with 21 survivors of childhood cancer. Two of the FGDs were with survivors ages 13-18 years old and four FGDs were with 19-25 years old. The discussions were recorded and then transcribed for data storage, management, and analysis. Results: The results consisted of information grouped into two broad categories as positive and negative experiences. Survivors of childhood cancer reported positive experiences during the post-treatment period. They experienced improvement in their physical condition (healthy lifestyle, better health), in psychosocial wellness (gratefulness, determination), and in sustained religious engagement (prayerfulness, involvement in religious activities). On the other hand, the survivors also reported negative posttreatment experiences. Their negative experiences were thematically clustered according to the broad areas of cognitive (inefficient memory retrieval), physical (limitations on physical activities, pain, body issues), and socio-emotional (worry about cancer in the family, fear of relapse, fear of rejection, irritability) aspects. Conclusion: The experiences of the survivors in the posttreatment have both positive and negative dimensions. However, the reported negative experiences seem to weigh heavily on the survivors, with numerous cognitive, physical and socio-emotional concerns. There is an increasing urgency to understand the posttreatment psychological needs of the growing population of childhood cancer survivors, and develop follow-up psychosocial interventions for them. These psychosocial interventions can equip survivors with strategies to effectively manage and overcome their chronic worries, instill confidence and a sense of security and be able to plan for their future more positively.
APA, Harvard, Vancouver, ISO, and other styles
4

Ang, Sin Hui, Serena Siew Lin Koh, Xiu Hua @. Hideka Tamamura Lee, and Shefaly Shorey. "Experiences of adolescents living with cancer: A descriptive qualitative study." Journal of Child Health Care 22, no. 4 (March 15, 2018): 532–44. http://dx.doi.org/10.1177/1367493518763109.

Full text
Abstract:
This study aimed to explore the experiences of adolescents from Singapore, aged 10–18 years old, living with cancer and their perceptions on how their psychosocial outcomes can be improved. A descriptive qualitative study design was used. Convenience sampling was used to recruit 10 participants from a pediatric oncology ward in a Singapore hospital. Individual semi-structured interviews were conducted. Thematic analysis was used to analyze the data. Five major themes emerged: (1) experience of physical symptoms, (2) emotional response to their condition, (3) changes in social dynamics, and (4) falling behind in academics. The psychosocial outcomes of Singaporean adolescents with cancer could be improved by thorough pain assessments and creating a more conducive hospital environment.
APA, Harvard, Vancouver, ISO, and other styles
5

Duggleby, Wendy, Dan Cooper, Cheryl Nekolaichuk, Laura Cottrell, Jenny Swindle, and Kelsi Barkway. "The psychosocial experiences of older palliative patients while participating in a Living with Hope Program." Palliative and Supportive Care 14, no. 6 (April 8, 2016): 672–79. http://dx.doi.org/10.1017/s1478951516000183.

Full text
Abstract:
AbstractObjective:Several studies have reported the effectiveness of a variety of psychosocial interventions in increasing levels of hope in palliative care patients. The experience of palliative patients while participating in these interventions is unknown. Understanding these experiences would provide a rich understanding of how the interventions work to foster hope. The purpose of the present study was to describe the psychosocial processes that participants with advanced cancer receiving palliative care experienced when taking part in a Living with Hope Program (LWHP).Method:In the context of a study evaluating the LWHP, data were collected from 13 dyads (persons with advanced cancer and their caregivers) at two timepoints (one week apart). A thematic qualitative analysis of 52 open-ended audiotaped interviews was conducted that focused on the psychosocial processes that occurred during the LWHP.Results:The average age of palliative participants was 67 (SD = 6.6) and of their family caregivers 61 years of age (SD = 13.9). A thematic analysis suggested that the participants experienced the following psychosocial processes while participating in the LWHP: (1) reminiscing, (2) leaving a legacy, (3) positive reappraisal, and (4) motivational processes. These processes are the mechanisms by which the LWHP fosters the positive outcomes of increasing hope and improving quality of life. As well, the finding of motivational processes suggested that the LWHP may also increase life satisfaction, which is an outcome of motivational processes.Significance of the results:The findings from our study underscore the importance of uncovering the psychosocial processes through which the LWHP works to foster hope. They will assist in making revisions to the intervention that will increase its effectiveness, as well as providing a better understanding of hope in persons with advanced cancer.
APA, Harvard, Vancouver, ISO, and other styles
6

Nedjat-Haiem, Frances R., Iraida V. Carrion, Karl A. Lorenz, Kathleen Ell, and Lawrence Palinkas. "Psychosocial Concerns among Latinas with Life-Limiting Advanced Cancers." OMEGA - Journal of Death and Dying 67, no. 1-2 (August 2013): 167–74. http://dx.doi.org/10.2190/om.67.1-2.t.

Full text
Abstract:
Research has demonstrated that limited dialogue in end-of-life (EOL) care can negatively impact decision-making and place of death. Furthermore, when vulnerable populations are faced with EOL cancer care, they experience issues resulting from previous gaps in services attributed to sociocultural and economic issues that influence EOL care. These conditions place an additional burden on disadvantaged populations which can cause distress, especially as disparate conditions continue to persist. Little is known about Latinos' psychosocial concerns that lead to distress in EOL care. The objective of this study is to explore Latinas' experiences with life-limiting cancer conditions to identify the EOL care concerns that impact their dying experience. This study used a phenomenological approach to explore the EOL care concerns of 24 Latinas receiving treatment for metastatic cancers in a public sector healthcare system in Los Angeles, California. In-depth interviews were recorded and transcribed, and qualitative analysis was performed using Atlas.ti software.
APA, Harvard, Vancouver, ISO, and other styles
7

Boles, Jessika, and Sarah Daniels. "Researching the Experiences of Children with Cancer: Considerations for Practice." Children 6, no. 8 (August 16, 2019): 93. http://dx.doi.org/10.3390/children6080093.

Full text
Abstract:
Children and adolescents with cancer often participate in medical and psychosocial research throughout their diagnosis and treatment. Furthermore, this involvement frequently extends into the survivorship period. Sometimes referred to as “doubly vulnerable” research participants, children and adolescents with cancer are not only minors, but also minors facing significant medical, developmental, and psychosocial stressors associated with chronic illness. Thus, it is important to exercise care in designing and conducting research with this population; however, these considerations have not been adequately addressed in pediatric healthcare literature. Therefore, the purpose of this review is to describe the research preferences and experiences of children and adolescents with cancer to identify techniques for supporting this population as research participants. By incorporating developmentally appropriate, context-specific, and child-centered adjustments, researchers can help children and adolescents with cancer effectively and meaningfully describe their illness experiences while also developing a positive outlook on future research participation.
APA, Harvard, Vancouver, ISO, and other styles
8

Wenger, Lisa M., and John L. Oliffe. "Moving Beyond the Prostate." American Journal of Men's Health 7, no. 2 (October 17, 2012): 138–41. http://dx.doi.org/10.1177/1557988312463420.

Full text
Abstract:
As researchers recognize the value in considering gender dynamics within the cancer experience, a majority of the masculinities work has centered on men with prostate cancer. This focus has positioned prostate cancer as the flagship of men’s cancer (and perhaps men’s health). There is value in this research. However, as 78% of men experience cancers of a different type, a narrow focus on prostate cancer does not necessarily account for broader intersections of cancer and masculinity. Argued here are the benefits to expanding the focus of research on men’s cancer experiences. As researchers consider patterns and diversities among men managing an array of cancers, there is opportunity to broaden understanding of the challenges “cancer” can present for men, disrupt assumptions that the study of men’s gendered experience of cancer must be tethered to male sex–specific biology, and enhance the relevance and impact of psychosocial interventions for men living with cancer.
APA, Harvard, Vancouver, ISO, and other styles
9

Bomar, Kaitlin, Elizabeth Willingham, Terra Dillard, Chad M. Dingman, Crystal Humphries, Stacey Kindall, Patricia D. Hegedus, James D. Bearden, and Hal E. Crosswell. "Bridging the gap in psychosocial care in cancer survivorship: A pilot project evaluating psychosocial interventions through telemedicine." Journal of Clinical Oncology 34, no. 3_suppl (January 20, 2016): 215. http://dx.doi.org/10.1200/jco.2016.34.3_suppl.215.

Full text
Abstract:
215 Background: Psychosocial distress is a well‐recognized consequence of cancer therapy, but psychosocial care for cancer survivors remains fragmented. Through the use of telemedicine, establishing an integrated, information technology‐based infrastructure between community‐based cancer programs may enhance coordination of survivorship care and increase psychosocial distress screening and intervention. We describe a one year pilot program intended to bridge institutional and geographic gaps in psychosocial intervention for cancer survivors through the use of telemedicine. Methods: There are 17 Commission on Cancer-accredited sites in South Carolina-only 31% of sites routinely conduct distress screening. This SC Cancer Alliance-supported pilot was designed as a quality care improvement project between two community-based cancer programs. The development and execution of the telemedicine project will be described. A survey-based, qualitative assessment of patient satisfaction with psychosocial intervention with between both physical and virtual counselling was performed and scored. Results: All patients seen in survivorship clinics at both institutions received psychosocial distress screening. By the end of the pilot project, 9 cancer survivors from the Spartanburg area were identified as having significant psychosocial distress, participated in counselling and reported on their experiences. Patients were seen either via face-to-face and/or virtual encounters. Counselling sessions performed via telemedicine were well accepted and that there was no difference in patient satisfaction as compared to face-to-face sessions. Anecdotal experiences and comments will be highlighted. Conclusions: Our pilot project demonstrates that psychosocial screening and intervention via telemedicine is feasible and may be effective at reducing psychosocial distress in cancer survivors. Psychosocial intervention via telemedicine may serve as a viable method of providing counselling services to resource poor areas, but significant barriers exist, including reimbursement, institutional variations in screening and care and information technology.
APA, Harvard, Vancouver, ISO, and other styles
10

Bonsu, Adwoa Bemah, Lydia Aziato, and Joe Nat A. Clegg-Lamptey. "Living with Advanced Breast Cancer among Ghanaian Women: Emotional and Psychosocial Experiences." International Journal of Palliative Care 2014 (June 25, 2014): 1–9. http://dx.doi.org/10.1155/2014/403473.

Full text
Abstract:
The purpose of this study was to explore the emotional and psychosocial experiences of Ghanaian women living with advanced breast cancer in the Kumasi metropolis. The study employed a qualitative exploratory descriptive design. Purposive sampling approach was used and data was saturated with 10 participants aged between 32 and 65 years. All interviews were audio-taped and transcribed. Data was analyzed concurrently based on the techniques of content analysis. Anonymity and confidentiality were ensured. Women experienced emotional reactions such as sadness, fear, and anxiety. Pain was severe and led to suicidal ideations. Women experienced lost hopes regarding their marriage, parenting, and work. They received support from their families, spouses, colleagues, health professionals, and spiritual leaders. Women coped by accepting the disease and surrendering to God and having the will to live. Five major themes described were emotional reactions, pain, lost hope, support, and coping. It was recommended that health care providers involved in breast cancer management should be trained to enhance effective and holistic care of women and their families. Also, patients with advanced disease should be given effective pain management and a multidisciplinary palliative care team should be instituted to care for the women.
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Psychosocial experiences of cancer"

1

Flynn, Samantha E. "Cancer experiences in people with intellectual disabilities." Thesis, University of Chester, 2018. http://hdl.handle.net/10034/621794.

Full text
Abstract:
People with intellectual disabilities are increasingly being diagnosed with cancer due, in part, to increases in life expectancy for this population. Despite the growing number of people with cancer and intellectual disabilities, the cancer-related experiences of people with intellectual disabilities are under-researched. Person-centred approaches to research are needed to better understand the needs and psychosocial outcomes of people with cancer and intellectual disabilities. This thesis aims to better understand the cancer-related experiences of people with intellectual disabilities, and the impact on the people who support them. The thesis comprises four related studies: (1) a systematic review of psychosocial experiences of cancer in people with intellectual disabilities; (2) a qualitative study of cancer experiences in people with intellectual disabilities using thematic analysis informed by grounded theory; (3) a survey of UK oncology nurses' attitudes and care perceptions towards people with intellectual disabilities; and (4) a feasibility study of an intervention to improve healthcare professionals' perceptions of communicating with people with cancer and intellectual disabilities. Five themes emerged from the ten papers included in the systematic review: delayed diagnosis; information, communication, and understanding; negative psychological consequences; negative physical consequences; and social support. Six of the ten papers included data from the same ethnographic study of 13 people, highlighting a paucity of empirical research regarding the psychosocial cancer experiences of people with intellectual disabilities. The qualitative study indicated that people with intellectual disabilities were often excluded from conversations about their diagnosis, treatment, and ongoing care, and expressed confusion and anxiety about their cancer. Attempts to protect them from distress inhibited communication, but where additional support was offered, participants engaged more meaningfully in their experience and this should, therefore, be encouraged. In the qualitative study, oncology nurses were reported to be important figures in the care of patients with intellectual disabilities. The survey of oncology nurses highlighted that caring for cancer patients with intellectual disabilities may intensify their already difficult role; however, previous experience may ameliorate negative consequences. This sample identified their need for training about communicating with people with intellectual disabilities. The first three studies informed the development of a novel, brief, online, video-based intervention for healthcare professionals working with people with intellectual disabilities and cancer. The feasibility trial of this intervention indicated that there were problems with recruitment, high attrition, and intervention adherence. These problems were, most likely due to participants finding the content and delivery method to be unacceptable. It is clear that the intervention is not feasible in its current format, and that further theoretical and modelling work is needed before the intervention is feasibility tested again ahead of a definitive trial. This body of work has demonstrated that people with intellectual disabilities and cancer face multiple barriers to accessing cancer care, including informative and understandable communication with healthcare professionals. With appropriate support, psychological and physical outcomes can be improved for people with intellectual disabilities and cancer, but caring for people with cancer and intellectual disabilities can be challenging for paid and informal carers, and oncology staff. Difficulties with communication are bi-directional, and improving communication might be an appropriate first step to improving cancer experiences for this population, but developing effective interventions presents numerous feasibility challenges.
APA, Harvard, Vancouver, ISO, and other styles
2

Chen, Chwen Cheng. "Psychosocial stress, coping style and the risk of breast cancer." Thesis, King's College London (University of London), 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.287787.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Simard, Sarah-Nicole. "Bridging the Gap – A Grounded Theory of Cancer Coaching Experiences." Thesis, Université d'Ottawa / University of Ottawa, 2016. http://hdl.handle.net/10393/34436.

Full text
Abstract:
Cancer incidence is increasing and so are survival rates. The aftermath of cancer includes multi-dimensional and long-lasting effects that prevent individuals from recovering and re-integrating into their daily routines. Cancer systems attend to patients during diagnosis and treatment, but often fall short in providing continuity of care afterward. This results in a considerable number of individuals living with the effects of cancer, with little support care. While there are evidence-based recommendations to improve follow-up cancer care, the extent to which they have been implemented remains unknown. To support the needs of cancer survivors The Ottawa Regional Cancer Foundation developed a Cancer Coaching Program (CCP). As life and health coaching interventions have been shown to benefit this population, this study aimed to explore the impacts of the CCP on the lives of cancer survivors. Using a grounded theory approach, the experiences of (n=12) cancer survivors who had previously participated in the program were explored, to create an explanatory model. Descriptive results depicted various beneficial outcomes to participating in the CCP. The dominant role of the CCP is to support survivors by “bridging the gap” to survivorship, through tailored coaching services. This study provides insight into the mechanisms that work for this cancer coaching program, which may be helpful for other programs exploring strategies to assist this population.
APA, Harvard, Vancouver, ISO, and other styles
4

Shermak, Sheryl Lee. "Diggin in, moving on : the experiences of breast cancer dragon boat paddlers." Thesis, University of British Columbia, 2008. http://hdl.handle.net/2429/2642.

Full text
Abstract:
It is commonly believed that breast cancer dragon boating benefits survivors in a range of psychosocial areas, but there have been few empirical studies to investigate such relationships. An interpretive description design and a critical health promotion approach were used to explore the psychosocial experiences of women who breast cancer dragon boat. In-depth interviews with six participants were analyzed. Themes that arose from the data are: (1) moving past isolation — networks of like-minded support, (2) taking control,(3) journey into adventure, (4) affirmative outlook, (5) confronting painful experience, (6) rebuilding identity, (7) and spiritual engagement. The findings illustrate that dragon boating provides breast cancer survivors with a significant venue for change and the opportunity to move beyond traumatic elements of cancer.
APA, Harvard, Vancouver, ISO, and other styles
5

Human, Carine. "The psychosocial experiences of the patient and family of skin cancer diagnosis and treatment." Diss., University of Pretoria, 2015. http://hdl.handle.net/2263/53411.

Full text
Abstract:
Skin cancer is the most common cancer in South Africa with about 20 000 reported cases every year and 700 deaths. The Cancer Association of South Africa (CANSA) urges all South Africans to be SunSmart to reduce the high incidence of skin cancer in the country. The World Health Organization (2014) reports that between two and three million non-melanoma skin cancers and approximately 132 000 malignant melanomas occur globally every year. South Africa has the second highest incidence of skin cancer in the world after Australia (CANSA, 2014). Skin cancer is an increasing phenomenon in South Africa and enough is not done to raise awareness. The researcher has a very personal interest in skin cancer, the emotions around it, the needs, thoughts and experiences of patients diagnosed with skin cancer, due to various family members having suffered skin cancer. The researcher also learnt through own experience that there is a lack of support systems for the traumatised family to fall back on, specifically when it comes to skin cancer. Individuals who wish to support the patient may also need education, support and information regarding the condition in order to do so. The latter was confirmed through consultations with a Dermatologist and a Plastic Surgeon with regards to the emotional effects of skin cancer. Both specialists expressed eagerness to learn more in this regard and committed to assist the researcher in this study in finding suitable participants, who were selected and interviewed. It was clear from the first interview that none of the participants had expected skin cancer and many emotions were expressed. When a person is diagnosed with skin cancer he or she will often experience anxiety which can be very severe. Anxiety may make the pain experienced by cancer sufferers worse. Anxiety is a normal response to stressful events and is part of the process of coming to terms with an illness. Fear of the unknown is often a significant cause of anxiety. Patients may feel less anxious when they are given more information about their illness and their treatment, or when they find out more from booklets available from cancer charities and patient groups or from websites. Patients also usually begin to feel less anxious as they become more accustomed to seeing the doctor and going to hospitals. As they get to know hospital staff they gradually feel more at ease and less threatened by fears of the unknown. (Gillie, 2005:42). The patient participants had some form of treatment for skin cancer. Various emotions and experiences were observed and expressed by both patient and family participants and it became evident that from diagnosis, through treatment and even post treatment, the participants had a lot of emotions and each phase brought along its own experiences, feelings and needs. This supported theory around the issue of skin cancer and the experience around it being studied. The emotional effects of cancer may last long after the end of treatment. People often find they continue to feel anxious about minor signs of illness or pain, fearing a recurrence. Regular check-ups may be necessary and these can be very scary times. Permanent changes in lifestyle, as a result of cancer, or bodily changes may be daily reminders of the cancer and cause sadness. As distressing as these emotions may be, they are natural reactions to a cancer diagnosis. Talking to family and friends may be helpful (The Cancer Council of New South Wales Coping with Cancer (2005:1). The researcher followed a qualitative approach in this study and attempted to understand the subjective life experience of the participants who suffer from skin cancer and have been diagnosed and undergone treatment. In order to add to the development of insight and a better understanding of the experiences skin cancer patients have in the current South African context, the researcher was able to obtain first-hand information through the use of unstructured interviews as it allowed the participants to share their thought and feelings and experience without guidance from the researcher. The information gathered was in the form of words and concepts, which gave meaning to the participants experiences of a skin cancer diagnosis and treatment. In total 13 participants were selected as part of the study, who included both skin cancer patients and family members. These participants were selected from existing patients and family members of patients of two private medical specialists in Panorama, Parow and Cape Town. Unstructured interviews were conducted with the participants and were voice recorded with their permission. These interviews were then transcribed. The data was then analysed by the researcher and from that, themes and sub-themes were identified. The research findings are presented by the biological profile of all the participants being portrayed and a thematic analysis of the themes and sub-themes. Literature and verbatim quotes were then given in support of the findings. Five themes were identified as follows: Theme 1: Lack of knowledge around skin cancer Theme 2: Reaction to diagnosis Theme 3: Treatment Theme 4: Post-diagnosis mindfulness and behaviour change and Theme 5: Support structures. Each theme had sub-themes which were also discussed. In conclusion, it was eminent that skin cancer patients and their family go through a lot of emotional turmoil and therefore it is of vital importance that the medical personnel or the multi-disciplinary team is aware of this when working with skin cancer patients. It was clear that at the point of diagnosis, patients and their families experience a lot of shock and disbelief which they have to work through. Some even have immediate fears of death, whereas others are oblivious of the severity of the condition. It was mentioned as a need from participants, but also noted in theory that knowledge or a good understanding of a condition and of the treatment lowers anxiety levels. All members of the multi-disciplinary team should ideally be aware and motivated to ensure patients emotional needs are identified and addressed. Social workers have a vital role to play as their skills to identify needs are highly developed and have a good understanding of the family as a support system, as well as connecting patients and families with support systems within their environment and community.
Mini Dissertation (MSW)--University of Pretoria, 2015.
Social Work and Criminology
MSW
Unrestricted
APA, Harvard, Vancouver, ISO, and other styles
6

Flack, Hazel June. "The psychosocial experiences of young people with cancer : a qualitative comparison between paediatric and adult treatment settings." Thesis, University of East Anglia, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.436523.

Full text
Abstract:
Qualitative methods were used to investigate the psychosocial experiences of young people (aged 13-21) with cancer (N=8). The experiences of young people treated in a paediatric ward were compared with those treated in adult wards. Data were collected using semi-structured interviews, observations and discussions with the treatment teams. The findings were considered in relation to two developmental theories of adolescence frequently used within this field of research: 1) Havighurst (1948), and 2) Erikson (1968). Four main themes emerged from the data: 1) personal (emotional and physical changes), 2) setting (the physical treatment environment), 3) relational (interactions with family, peers, other patients and the treatment team), and 4) education, career and the future. Differences emerged between the treatment wards in relation to young people's psychosocial experiences. The theoretical implications of the research are considered and the researcher questions the usefulness of these developmental theories within the context of young people with cancer. Alternative theories (including ideas from: positive psychology, models of chronic illness, and systemic theory) are proposed to enhance our understanding of young people's experiences during treatment. The research also discusses clinical implications, including how to enhance the provision of psychosocial care for young people with cancer.
APA, Harvard, Vancouver, ISO, and other styles
7

Larson, Cheryl Ann Davisson. "Spiritual, psychosocial, and physical correlates of well-being across the breast cancer experience." Diss., The University of Arizona, 2004. http://hdl.handle.net/10150/280719.

Full text
Abstract:
Spirituality has gained increasing attention by scientists for its importance in contributing to understanding human health experiences. The purpose of this study was to examine the relationships of spiritual, psychosocial, and physical correlates to well-being and depression over the trajectory of breast cancer experience. Nursing theory, lifespan development, and chronic illness trajectory provided the conceptual framework for the study. A correlational, retrospective design was used allowing for collection of longitudinal data during a one-time measurement process. The sample consisted of 64 women (constituting a 91% response rate) 60 years or older with Stage I, II, or III breast cancer, who had chemotherapy and/or radiation, and were 8 to 24 months post treatment. A set of questionnaires was used to obtain data over three phases of their breast cancer experience: Anticipatory; Therapy; and Survivor. For data analysis, it was determined that all instruments had adequate reliability and validity, and statistical assumptions were met. Multiple regression results indicated that two variables in particular (self-transcendence and symptom distress) were consistently significant in explaining well-being and depression (with explained variance ranging from 57% to 85%) across all three phases. Other variables (hope, spiritual perspective, social support) also contributed significantly to the explained variance across some phases. Repeated Measure ANOVA and post hoc tests indicated that the scores on several variables differed significantly depending upon the phase of illness. While symptom distress is often a primary concern of patient and nurse, it was concluded that spiritual variables are also important factors in experiences of well-being and depression across the trajectory of the illness. A second conclusion was that, as with physical or social aspects, spirituality includes many dimensions of human experience and should be studied for the variety of spiritual factors that may be significant across the trajectory of illness. In this study, at least one or more different spiritual variables were significant in the regression equations for every phase of illness. Findings provided empirical evidence to refine and further develop a mid-range theory on how spirituality functions as an important resource for well-being within the context of other variables, across the breast cancer experience.
APA, Harvard, Vancouver, ISO, and other styles
8

Lloyd, Susannah. "Understanding the experience of prophylactic bilateral mastectomy : a grounded theory study." Thesis, University of East Anglia, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.302194.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Schüttler, Johanna, and Hanna Samuelsson. "Ung vuxen med cancer - behov och upplevelser under och efter behandling : En litteraturstudie." Thesis, Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-368292.

Full text
Abstract:
Background: In Sweden, approximately 800 young adults between 16-30 years of age are affected by a cancer disease. Studies has shown that this is not only the medical treatment that affects how patients live with their cancer, but also how their psychological health are affected. When a young adult gets a cancer diagnosis can thoughts about the disease, death, changed body image, loss of fertility etcetera be particularly disturbing and anxiety evoking. To achieve good health and quality of life, care and good relations between patient and nurses are important. Aim: The aim of the literature study was to: 1) Examine young adults experiences of a cancer disease, 2) Experienced need of support from healthcare professionals and 3) Experiences of psychosocial support from nurses during and after treatment. Method: A literature study where qualitative articles were searched through the database Pubmed. 10 original articles out of a total of 27 articles were included because they met the inclusion criteria and were either medium or high quality. Results: The analysis revealed nine themes based on the three questions; attitudes and emotional reactions related to the disease, changed perception of identity, positive aspects of the disease, post-treatment reactions, support from family and friends, support and adaptation within health care, informative support, personal and emotional support and participation and trust. The need for information from healthcare professionals was particularly prominent, especially on the topics of sexuality and fertility. The importance of obtaining information in a manner that is easy to understand was highlighted. The majority of young adults experienced positive support from nurses which made them gain confidence, trust and joy. Conclusion: Young adults have an increased need for continuous information and guidance during and after treatment. Nurses need to be better at communicating, which would contribute to increased understanding and provide security for the patient in order to feel better mentally. Nurses have an important role in providing advice and information in areas which the patient lack knowledge in.
APA, Harvard, Vancouver, ISO, and other styles
10

Foster, Charles A. "Getting Back to My Life: Exploring Adaptation to Change Through the Experiences of Breast Cancer Survivors." Antioch University / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=antioch1338575681.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Books on the topic "Psychosocial experiences of cancer"

1

Baum, Andrew, and Barbara L. Andersen, eds. Psychosocial interventions for cancer. Washington: American Psychological Association, 2001. http://dx.doi.org/10.1037/10402-000.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

University of Texas M.D. Anderson Cancer Center, ed. MD Anderson handbook of psychosocial oncology. New York: McGraw-Hill, 2010.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
3

British Psychosocial Oncology Group. Conference. Psychosocial oncology: Proceedings of the Second and Third Meetings of the British Psychosocial Oncology Group, London and Leicester, 1985 and 1986. Edited by Watson M, Greer S, Thomas C, and British Psychosocial Oncology Group. Conference. Oxford: Pergamon Press, 1988.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
4

Idemudia, Erhabor, and Klaus Boehnke. Psychosocial Experiences of African Migrants in Six European Countries. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-48347-0.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Irvine, Diane. Investigating psychosocial adjustment in breast cancer: A discussion paper. Ottawa, Ontario: Health Canada, 1997.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
6

Shelley, Currie. The Alberta Cancer Board Psychosocial Oncology Network: Provincial framework. [Edmonton]: Alberta Cancer Board, 2003.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
7

1947-, Watson M., Greer S, Thomas C, and British Psychosocial Oncology Group (Conference), (3rd : 1986 : Leicester), eds. Psychosocial oncology: Proceedings of the second and third meetings of the British Psychosocial Oncology Group, London and Leicester, 1985 and 1986. Oxford: Pergamon, 1987.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

1947-, Watson M., and Greer S, eds. Psychosocial issues in malignant disease: Proceedings of the first annual conference. Oxford: Pergamon, 1986.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
9

Pollack, Alan, and Mansoor M. Ahmed. Hypofractionation: Scientific concepts and clinical experiences. Ellicott City, MD: LumiText Publishing, 2011.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
10

National Cancer Control Initiative (Australia), ed. Clinical practice guidelines for the psychosocial care of adults with cancer. [Canberra?]: NHMRC, 2003.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Book chapters on the topic "Psychosocial experiences of cancer"

1

Tang, Michael H. "In Their Own Voices: Experiences of Children and Adolescents with Cancer." In Pediatric Psychosocial Oncology: Textbook for Multidisciplinary Care, 387–90. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-21374-3_23.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Alfano, Catherine M., and Julia H. Rowland. "The experience of survival for patients: Psychosocial adjustment." In Handbook of cancer control and behavioral science: A resource for researchers, practitioners, and policymakers., 413–30. Washington: American Psychological Association, 2009. http://dx.doi.org/10.1037/14499-023.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Fentiman, Ian. "Psychosocial." In Male Breast Cancer, 97–104. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-04669-3_7.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Weihs, Karen. "Psychosocial Oncology." In Supportive Cancer Care, 45–55. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-24814-1_3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Hulbert-Williams, Nicholas, and Gill Hubbard. "Psychosocial Adjustment to Cancer." In Cancer and Cancer Care, 272–82. 1 Oliver’s Yard, 55 City Road London EC1Y 1SP: SAGE Publications Ltd, 2015. http://dx.doi.org/10.4135/9781473920620.n18.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Penedo, Frank J., Catherine Benedict, and Bonnie McGregor. "Cancer: Psychosocial Treatment." In Encyclopedia of Behavioral Medicine, 319–25. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-1005-9_156.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Penedo, Frank J., Catherine Benedict, and Bonnie McGregor. "Cancer: Psychosocial Treatment." In Encyclopedia of Behavioral Medicine, 358–65. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-39903-0_156.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Kennedy, Fiona, and Nicholas Hulbert-Williams. "Psychosocial Research in Cancer Care." In Cancer and Cancer Care, 500–516. 1 Oliver’s Yard, 55 City Road London EC1Y 1SP: SAGE Publications Ltd, 2015. http://dx.doi.org/10.4135/9781473920620.n33.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Braš, Marijana, and Veljko Đorđević. "Psychosocial Aspects of Cancer Pain." In Cancer Pain, 211–19. London: Springer London, 2013. http://dx.doi.org/10.1007/978-0-85729-230-8_16.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Singer, Susanne. "Psychosocial Impact of Cancer." In Recent Results in Cancer Research, 1–11. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-64310-6_1.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Psychosocial experiences of cancer"

1

Quilty, Caroline, and Jonathan Koffman. "P-172 Psychosocial experience of weight loss in cancer cachexia. what can health care professionals learn?" In Leading, Learning and Innovating, Hospice UK 2017 National Conference, 22–24 November 2017, Liverpool. British Medical Journal Publishing Group, 2017. http://dx.doi.org/10.1136/bmjspcare-2017-hospice.197.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Savitri, Wenny, and Amin Haryati. "Psychosocial Distress in Breast Cancer Patients." In International Conference on Health and Medical Sciences (AHMS 2020). Paris, France: Atlantis Press, 2021. http://dx.doi.org/10.2991/ahsr.k.210127.032.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Gomes, Ana Sofia. "Maltreatment experiences and depression in adolescents: The moderating effect of psychosocial functioning." In 3th International Conference on Cognitive - Social, and Behavioural Sciences. Cognitive-crcs, 2015. http://dx.doi.org/10.15405/epsbs.2015.08.6.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Candido, Maria Joao, Ana Bartolo, and Sara Monteiro. "Reproductive concerns and psychosocial adjustment of young breast and gynecologic cancer patients." In 2nd icH&Hpsy International Conference on Health and Health Psychology. Cognitive-crcs, 2016. http://dx.doi.org/10.15405/epsbs.2016.07.02.22.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Im, YR, RE Phillips, and A. Gite. "G553(P) ‘back to school’: the psychosocial impact on children with cancer." In Royal College of Paediatrics and Child Health, Abstracts of the RCPCH Conference and exhibition, 13–15 May 2019, ICC, Birmingham, Paediatrics: pathways to a brighter future. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2019. http://dx.doi.org/10.1136/archdischild-2019-rcpch.536.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Priday, G. "G51(P) The psychosocial needs of teenagers and young people with cancer." In Royal College of Paediatrics and Child Health, Abstracts of the Annual Conference, 24–26 May 2017, ICC, Birmingham. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2017. http://dx.doi.org/10.1136/archdischild-2017-313087.50.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Malmqvist, Jessica, Volkert Siersma, Mie Hestbech, and John Brodersen. "31 Psychosocial consequences of participating in a national colorectal cancer screening programme." In Preventing Overdiagnosis, Abstracts, August 2018, Copenhagen. BMJ Publishing Group Ltd, 2018. http://dx.doi.org/10.1136/bmjebm-2018-111070.31.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Fallowfield, LJ. "Abstract PL03: Psychosocial, survivorship issues: Are we doing better?" In Abstracts: Thirty-Sixth Annual CTRC-AACR San Antonio Breast Cancer Symposium - Dec 10-14, 2013; San Antonio, TX. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/0008-5472.sabcs13-pl03.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Jones, Jeffrey, and Allison Hart-Young. "EXPLORING PSYCHOSOCIAL EXPERIENCES AND OUTCOMES OF COLLEGE MENTORS ENGAGED IN A COMMUNITY SERVICE AND SOCIAL ACTION PROGRAM." In International Technology, Education and Development Conference. IATED, 2016. http://dx.doi.org/10.21125/iceri.2016.2107.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Cheng, Yawen. "843 Emerging psychosocial work hazards and evolving policy actions: experiences of taiwan and other east asian countries." In 32nd Triennial Congress of the International Commission on Occupational Health (ICOH), Dublin, Ireland, 29th April to 4th May 2018. BMJ Publishing Group Ltd, 2018. http://dx.doi.org/10.1136/oemed-2018-icohabstracts.13.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Reports on the topic "Psychosocial experiences of cancer"

1

Hull, Pamela C. Psychosocial and Cultural Barriers to Prostate Cancer Screening: Racial Comparisons. Fort Belvoir, VA: Defense Technical Information Center, March 2008. http://dx.doi.org/10.21236/ada485653.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Poole, Elizabeth M. Psychosocial Stress and Ovarian Cancer Risk: Metabolomics and Perceived Stress. Fort Belvoir, VA: Defense Technical Information Center, October 2014. http://dx.doi.org/10.21236/ada613203.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Brewster, Abenaa, Susan Peterson, Scott Cantor, Robert Volk, Yu Shen, Isabelle Bedrosian, Herbert Dupont, and Patricia Parker. Contralateral Prophylactic Mastectomy and Breast Cancer: Clinical and Psychosocial Outcomes. Patient-Centered Outcomes Research Institute (PCORI), October 2018. http://dx.doi.org/10.25302/10.2018.ce.13046293.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Hull, Pamela C. Psychosocial and Cultural Barriers to Prostate Cancer Screening: Racial Comparisons. Fort Belvoir, VA: Defense Technical Information Center, March 2007. http://dx.doi.org/10.21236/ada470085.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Hull, Pamela C. Psychosocial and Cultural Barriers to Prostate Cancer Screening: Racial Comparisons. Fort Belvoir, VA: Defense Technical Information Center, March 2009. http://dx.doi.org/10.21236/ada511620.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Taylor, C. B., and Andrew J. Winzelberg. The Development and Evaluation of an Innovative Internet-Based Breast Cancer Psychosocial Intervention. Fort Belvoir, VA: Defense Technical Information Center, October 2001. http://dx.doi.org/10.21236/ada403662.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Taylor, C. B. The Development and Evaluation of an Innovative Internet-Based Breast Cancer Psychosocial Intervention. Fort Belvoir, VA: Defense Technical Information Center, October 2000. http://dx.doi.org/10.21236/ada392283.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Coyne, James C. Using the Internet to Collaborate with Consumers in Redefining a Psychosocial Agenda for Families with Hereditary Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, June 2007. http://dx.doi.org/10.21236/ada473796.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Shapiro, Pamela J., James C. Coyne, David J. Vaughn, and Rosette P. Biester. Cognitive Performance, Quality of Life, and Psychosocial Adjustment Among Men Receiving Androgen Deprivation Therapy for Treatment of Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, April 2005. http://dx.doi.org/10.21236/ada437272.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Shapiro, Pamela J. Cognitive Performance Quality of Life and Psychosocial Adjustment Among Men Receiving Androgen Deprivation Therapy for Treatment of Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, April 2004. http://dx.doi.org/10.21236/ada428002.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Psychosocial experiences of cancer' for particular source types:
Journal articles Dissertations / Theses Books
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography