Abstract:Background: Adjustment to cancer as a stressful event is affected by bio-psycho-social factors. Objectives: This study aimed to investigate stigma phenomenon, the process of formation, and its impact on cancer patients and their families. Methods: This research was conducted based on the grounded theory study. Semi-structured interview was used with 12 cancer patients (7 women and 5 men), one of the immediate family members (spouse, parent or sibling) and 8 oncology staff members. Participants were selected in… Show more
“…More specifically, the “amount” of SS can be reduced in cultures where such beliefs prevail. Indeed, in Iranian culture, an individual may be less likely to seek out SS (Mohabbat-bahar et al, 2017). Patients and their family are less likely to engage in help-seeking, as it is deemed that the cancer is a result of the individual's or his or her family's past actions, and they are, therefore, less deserving of being given support (Ehsani et al, 2016; Mohabbat-bahar et al, 2017).…”
Section: Introductionmentioning
confidence: 99%
“…In some societies, illness and especially cancer are interpreted as the result of a person's or a family's actions, and it can, therefore, affect the amount of SS that it is believed that the individual "deserves" (Hasan Shiri et al, 2018). More specifically, within Iran, cancer is associated with fears of contagion and may often be attributed to family genetic defects, misfortune, fate, wrongdoing, and even being cursed (Mohabbat-bahar et al, 2017). Thus, Iranian patients and their families tend to hide their diagnosis from others.…”
Section: Introductionmentioning
confidence: 99%
“…Thus, although the mother may require SS as an assistive resource, cultural beliefs within these countries attract more stigma to the family experiencing such a crisis and mothers may, therefore, feel reluctant in calling upon potential SS networks. Within these cultures, there is great reluctance to seek SS outside of the context of the immediate family (Mohabbat-bahar et al, 2017). When a family member is sick, while relatives may come to the aid of the family, the mother is still precluded from seeking SS outside of the family from, for example, friends and colleagues.…”
Objective
The present study examined the extent to which social support (SS) availability and satisfaction could predict the extent of caregiver burden (CB) among mothers of children with Acute Lymphocytic Leukemia (ALL).
Method
The study was a cross-sectional, descriptive-correlative study. It was conducted on a sample of 117 mothers whose children were undergoing treatment in a public hospital in Bam, Iran. The Norbeck Social Support Scale and the Caregiver Burden Scale were used to measuring study variables. The data were analyzed using Pearson's correlations, t-tests, ANOVAs, and linear regressions.
Results
Significant correlations were observed between CB and SS availability (r = −0.499, p < 0.001), SS satisfaction (r = −0.543, p < 0.001), the age of the child with cancer (r = −0.22, p = 0.01), and duration of treatment (r = 0.336, p < 0.001). Married mothers experienced less CB than those that were widowed or divorced. Within the regression equation, SS satisfaction, SS availability, marital status, and duration of treatment were the predictors of CB.
Significance of results
Based on the results of the current study, mothers who have less SS, especially those who are single mothers, with younger children, and who have taken care of their child for an extended duration should be given special attention. Furthermore, it appears that there are distinct cultural variations amongst Iranian mothers which suggest that culture may impact upon SS availability. Results also suggest a need for interventions that enhance nurses' ability to provide support to caregivers and the broader family unit as a whole. Nurses in cancer care need to have psychological competencies to help family members of cancer patients especially mothers and more so those that are single mothers. As integral members of the patient care experience, nurses may be uniquely positioned to provide this needed psychosocial support.
“…More specifically, the “amount” of SS can be reduced in cultures where such beliefs prevail. Indeed, in Iranian culture, an individual may be less likely to seek out SS (Mohabbat-bahar et al, 2017). Patients and their family are less likely to engage in help-seeking, as it is deemed that the cancer is a result of the individual's or his or her family's past actions, and they are, therefore, less deserving of being given support (Ehsani et al, 2016; Mohabbat-bahar et al, 2017).…”
Section: Introductionmentioning
confidence: 99%
“…In some societies, illness and especially cancer are interpreted as the result of a person's or a family's actions, and it can, therefore, affect the amount of SS that it is believed that the individual "deserves" (Hasan Shiri et al, 2018). More specifically, within Iran, cancer is associated with fears of contagion and may often be attributed to family genetic defects, misfortune, fate, wrongdoing, and even being cursed (Mohabbat-bahar et al, 2017). Thus, Iranian patients and their families tend to hide their diagnosis from others.…”
Section: Introductionmentioning
confidence: 99%
“…Thus, although the mother may require SS as an assistive resource, cultural beliefs within these countries attract more stigma to the family experiencing such a crisis and mothers may, therefore, feel reluctant in calling upon potential SS networks. Within these cultures, there is great reluctance to seek SS outside of the context of the immediate family (Mohabbat-bahar et al, 2017). When a family member is sick, while relatives may come to the aid of the family, the mother is still precluded from seeking SS outside of the family from, for example, friends and colleagues.…”
Objective
The present study examined the extent to which social support (SS) availability and satisfaction could predict the extent of caregiver burden (CB) among mothers of children with Acute Lymphocytic Leukemia (ALL).
Method
The study was a cross-sectional, descriptive-correlative study. It was conducted on a sample of 117 mothers whose children were undergoing treatment in a public hospital in Bam, Iran. The Norbeck Social Support Scale and the Caregiver Burden Scale were used to measuring study variables. The data were analyzed using Pearson's correlations, t-tests, ANOVAs, and linear regressions.
Results
Significant correlations were observed between CB and SS availability (r = −0.499, p < 0.001), SS satisfaction (r = −0.543, p < 0.001), the age of the child with cancer (r = −0.22, p = 0.01), and duration of treatment (r = 0.336, p < 0.001). Married mothers experienced less CB than those that were widowed or divorced. Within the regression equation, SS satisfaction, SS availability, marital status, and duration of treatment were the predictors of CB.
Significance of results
Based on the results of the current study, mothers who have less SS, especially those who are single mothers, with younger children, and who have taken care of their child for an extended duration should be given special attention. Furthermore, it appears that there are distinct cultural variations amongst Iranian mothers which suggest that culture may impact upon SS availability. Results also suggest a need for interventions that enhance nurses' ability to provide support to caregivers and the broader family unit as a whole. Nurses in cancer care need to have psychological competencies to help family members of cancer patients especially mothers and more so those that are single mothers. As integral members of the patient care experience, nurses may be uniquely positioned to provide this needed psychosocial support.
“…Qualitative studies have yielded similar results to quantitative studies. [152930] However, the studies referred to above mainly reflect results obtained from socioculturally and economically developed countries. [45121823] Cross-cultural myths can also affect negative attitudes toward cancer.…”
Objective:The aim of the current study are to determine the depression levels of adult oncology patients in the cancer treatment phase and identify both cancer-related stigma and the factors affecting their depression levels.Methods:In this correlational study, 303 adult patients who had been treated at a medical outpatient clinic were surveyed using the convenience sampling method. The “questionnaire for measuring attitudes toward cancer – patient version,” a sociodemographic characteristics questionnaire, and the beck depression inventory were used. A multivariable linear regression model was used for the analysis.Results:The questionnaire and its subscale scores indicated a positive relationship between depression and attitudes toward cancer. The predictive variables for depression were “being younger than 40-year-old” and “feelings of social exclusion,” which accounted for 4% of the total variance. Four factors indicating negative attitudes toward cancer were “being more than 60-year-old,” “higher education,” “low income,” and “feelings of social exclusion,” which accounted for 11% of the total variance.Conclusions:Cancer-related stigma, which underlies patients' emotional and behavioral outlooks, should be reduced in cancer patients. Members of health teams should be sensitive to cancer-related stigma.
“…The image of death, bad fate, disaster and misery are some parts of attitude toward cancer [9]. In addition to the human health threat, cancer may be a deviation from the norm and an undesirable quality and the affected person can be exposed to negative emotions of others [5] [10].…”
Purpose: Disease-related Stigma is negative emotions, attitudes, stereotypes, and beliefs about diseases. Cancer is one of the diseases that can be exposed to stigma. Regarding the effects of stigma on the quality of life; admission and adherence to treatment, and considering stigma as a barrier to health promotion and cancer screening, the aim of this study was to provide a care plan for reducing stigma in cancer. Methods: This research was carried out during three phases of qualitative, quantitative studies and a review of the literature. The qualitative phase was conducted by conventional content analysis to find effective factors on the reduction of stigma through face to face semi-structured interviews. The quantitative phase was a cross-sectional descriptive study to measure the level of stigma. By using both quantitative and qualitative findings, and a review of the literature, a comprehensive care plan to reduce stigma in families with cancer patients was developed. Results: The results showed two categories of data; 1) reducing stigma at the individual or family level which needs increasing awareness, teaching coping skills, and support, as well as counseling; and 2) stigma reduction at the community level and policy rules which involve public education and cultural changes. Conclusion: Implementation of a care plan for reducing stigma can increase the physical and psychological health outcomes of people influenced by cancer, and at the community level, improves the attitude toward cancer and the success of screening programs, and ultimately reduces disability and mortality of the disease.
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