Journal of Psychosocial Oncology Impact Factor & Information

Publisher: Taylor & Francis (Routledge)

Journal description

Now in its eighteenth exciting year of publication, the Journal of Psychosocial Oncology is the first multidisciplinary journal published specifically for health professionals responsible for the psychosocial needs of cancer patients and their families. This forum provides for the rapid publication of new clinical and research material to help advance clinical and helping skills, as well as exploratory, hypothesis testing, and program evaluation research on such critical areas as the stigma of cancer, employment and personal problems facing cancer patients, patient education, family involvement in patient care, children with cancer, psychosocial needs of cancer patients, hospital and hospice staff, and volunteers. The journal covers all aspects of psychosocial care of the cancer patient from infancy through geriatrics. The distinguished editorial board includes representatives from many different fields in psychosocial oncology, including education, epidemiology, health advocacy, medical oncology, neurology, nursing, nutrition, pastoral counseling, physical therapy, psychiatry, psychology, public health, social work, sociology, and surgical oncology. Special columns and sections featured in the Journal of Psychosocial Oncology include: discussions of current ethical, philosophical, and existential issues for the psychosocial oncology specialist; a column on research issues, strategies, and methodologies in psychosocial oncology; announcements of current meetings, symposia, and courses offered in psychosocial oncology; book reviews that highlight important, new book-length works dealing with specific areas of psychosocial oncology; a selective bibliography of psychosocial oncology articles appearing in other journals.

Current impact factor: 1.04

Impact Factor Rankings

Additional details

5-year impact 1.38
Cited half-life 9.20
Immediacy index 0.09
Eigenfactor 0.00
Article influence 0.46
Website Journal of Psychosocial Oncology website
Other titles Journal of psychosocial oncology (Online), Journal of psychosocial oncology
ISSN 1540-7586
OCLC 50132408
Material type Document, Periodical, Internet resource
Document type Internet Resource, Computer File, Journal / Magazine / Newspaper

Publisher details

Taylor & Francis (Routledge)

  • Pre-print
    • Author can archive a pre-print version
  • Post-print
    • Author can archive a post-print version
  • Conditions
    • Some individual journals may have policies prohibiting pre-print archiving
    • On author's personal website or departmental website immediately
    • On institutional repository or subject-based repository after either 12 months embargo
    • Publisher's version/PDF cannot be used
    • On a non-profit server
    • Published source must be acknowledged
    • Must link to publisher version
    • Set statements to accompany deposits (see policy)
    • The publisher will deposit in on behalf of authors to a designated institutional repository including PubMed Central, where a deposit agreement exists with the repository
    • STM: Science, Technology and Medicine
    • Publisher last contacted on 25/03/2014
    • This policy is an exception to the default policies of 'Taylor & Francis (Routledge)'
  • Classification
    ‚Äč green

Publications in this journal

  • Journal of Psychosocial Oncology 09/2015; 33(5):599-601. DOI:10.1080/07347332.2015.1073056
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    ABSTRACT: The importance of training non-psychology healthcare professionals to offer psychological support to people with cancer is becoming increasingly recognised. This small scale pilot project sought to identify the training and support needs of oncology staff, and evaluate the effectiveness of a Level 2 Psychological Support Training Programme workshop. Semi-structured interviews with five members of multidisciplinary oncology staff identified that training needs were primarily around communication skills, recognising and dealing with emotions, offering support and empathy, and self-care. Pre and post-training questionnaires developed with these themes in mind revealed that the Level 2 Training Programme workshops run in this network of hospitals are effective in increasing participants' levels of perceived knowledge and confidence across each of these domains. Recommendations are made for further enhancing this effectiveness.
    Journal of Psychosocial Oncology 08/2015; DOI:10.1080/07347332.2015.1082170
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    ABSTRACT: Research suggests that spiritual well-being positively contributes to quality of life during and following cancer treatment. This relationship has not been well-described in ethnically diverse survivors of allogeneic transplantation. This study compares spiritual well-being and quality of life of Hispanic (n = 69) and non-Hispanic (n = 102) survivors. Hispanic participants were significantly younger, and reported significantly greater spiritual well-being than non-Hispanic survivors. Survivors with higher spiritual well-being had significantly better quality of life. Meaning and Peace significantly predicted quality of life. Although Hispanic survivors report greater spiritual well-being, Meaning and Peace, irrespective of ethnicity, have a salutary effect on quality of life.
    Journal of Psychosocial Oncology 08/2015; DOI:10.1080/07347332.2015.1082167
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    ABSTRACT: Social cognitive theory (SCT) measures related to exercise adherence in head and neck cancer (HNCa) patients were developed. Enrolling 101 HNCa patients, psychometric properties and associations with exercise behavior were examined for barriers self-efficacy, perceived barriers interference, outcome expectations, enjoyment, and goal setting. Cronbach's alpha ranged from .84 to .95; only enjoyment demonstrated limited test-retest reliability. Subscales for barriers self-efficacy (motivational, physical health) and barriers interference (motivational, physical health, time, environment) were identified. Multiple SCT constructs were cross-sectional correlates and prospective predictors of exercise behavior. These measures can improve the application of the SCT to exercise adherence in HNCa patients.
    Journal of Psychosocial Oncology 07/2015; DOI:10.1080/07347332.2015.1067277
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    ABSTRACT: The goal of the present research is to investigate and analyze possible peculiarities of the psychological state of cancer patients undergoing treatment. Scores characterizing the trait and state anxiety were acquired using Integrative Anxiety Test from four groups: adults with no appreciable disease, pregnant women, cancer patients examined during the specific antitumour treatment, and cancer patients brought into lasting clinical remission. Statistical analysis of the testing results revealed the bimodal type of the distribution of scores. The only statistically significant exception was the distribution of the state anxiety scores in cancer patients undergoing treatment that was clearly unimodal.
    Journal of Psychosocial Oncology 07/2015; DOI:10.1080/07347332.2015.1067280
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    ABSTRACT: The goal of this study was to determine the relationship between sexual adjustment, mastery, age, subjective health, and changes in sexual satisfaction in cancer patients receiving chemotherapy. A cross-sectional descriptive correlation study was conducted with a convenience sample comprising cancer patients who were visiting two cancer centers in Korea. Data were collected using self-report questionnaires, including the Global Sexual Satisfaction Index (GSSI) and sexual adjustment subscale of the Psychosocial Adjustment to Illness Scale (PAIS). The Mastery Scale was used to assess self-control. The hypothesized model was tested using a path analysis with AMOS 17.0. The path model was used to investigate causal relationships between variables, to obtain maximum-likelihood estimates of model parameters, and to provide goodness-of-fit indices. The proposed path model showed a good fit to the data. Subjective health and age may have an effect, mediated by mastery, on sexual adaption. Participants who reported more decreased sexual satisfaction showed lower levels of sexual adjustment. Mastery was not a mediating factor between changes in sexual satisfaction and sexual adjustment. Our model provides a framework for improving sexual adaption in cancer patients with chemotherapy. Health professionals should recognize and assess prior sexual satisfaction and sexual problems when providing sexual health care during treatment.
    Journal of Psychosocial Oncology 07/2015; DOI:10.1080/07347332.2015.1067278
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    ABSTRACT: Despite increasing utilization of hospice care, older adults with cancer enroll in hospice for shorter periods of time than those with other life-limiting illnesses. How older adults with cancer and their family members consider hospice is unknown. The purpose of this study was to compare decision-making in late-stage cancer in people who enrolled in hospice with those who declined. Concepts from the Carroll and Johnson (1990) decision-making framework guided the development of a hospice decision-making model. The study design was exploratory-descriptive, cross-sectional and used a 2-group comparison. Qualitative and quantitative data were collected in the same interview. Open-ended questions were used to explore the illness trajectory and decision-making process. The interrelationships between functional ability, quality of life and social support with hospice decision-making were assessed using the Katz, QLQ-30 and Lubben Social Network Scales. Study participants included 42 older adults with cancer who had been offered hospice enrollment (24 non-hospice and 18 hospice) and 38 caregivers (15 non-hospice and 23 hospice); N=80. The decisional model illustrates that the Recognition of Advanced Cancer and Information and Communication Needs were experienced similarly by both groups. There was interaction between the decisional stages: Formulation of Awareness and Generation of Alternatives that informed the Evaluation of Hospice but these stages were different in the hospice and non-hospice groups. The hospice enrollment decision represents a critical developmental juncture which is accompanied by a transformed identity and substantive cognitive shift. Increased attention to the psychosocial and emotional issues that accompany this transition are important for quality end-of-life care.
    Journal of Psychosocial Oncology 07/2015; DOI:10.1080/07347332.2015.1067282
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    ABSTRACT: Objective: The long-term psychosocial impact of adult daughters caring for their mothers with breast cancer has been recognized but understudied. The objectives of this study were to characterize the psychosocial functioning of women who served as informal caregivers during their mothers. treatment for breast cancer in two distinct samples, community and high risk clinic, and to determine differences in psychosocial functioning between the two samples. Methods: Using a cross-sectional design, a sample of mostly married, Caucasian and college educated women (N = 59) were administered a battery of questionnaires assessing socio-demographic and psychosocial factors (i.e. coping, caregiving tasks and difficulty, social support, spirituality, mental distress, depressive symptoms). Results: Using descriptive analysis, chi-square and T tests, results demonstrated significant differences between the two samples in time since caregiving, with the community sample reporting few years since the caregiving episode (e.g. 2.1 versus 15.1 years); coping strategies, with the clinic sample reporting higher scores on active coping, behavioral disengagement, planning, and self-blame; support type care tasks difficulty, with the clinic sample reporting higher scores on emotional support and tangible support, and all domains of spirituality (e.g. peace, meaning, faith), with higher levels being reported by the community sample. Although participants did not exhibit clinically significant levels of emotional distress, almost 25% of the community sample and 10% of the clinic sample had clinically significant depressive symptoms. Conclusions: Findings underscore the need for interventions tailored for caregivers to consider the unique psychosocial characteristics of caregivers across settings.
    Journal of Psychosocial Oncology 07/2015; 33(5). DOI:10.1080/07347332.2015.1067281
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    ABSTRACT: Breast cancer survivors commonly experience fatigue, but family-focused interventions as a means to reduce fatigue are understudied. This qualitative study explored the experience of adding a family component to a multi-modal group intervention for fatigue. Data were collected from group observations, in-depth interviews, and debriefing sessions with the program social worker. Fourteen survivors completed the family intervention (mean age 57 years) with a family member or close friend. Four themes associated with the family intervention were identified: (a) importance of family inclusion, (b) education of family members about fatigue, (c) enhanced family communication, and (d) family partnership to combat fatigue.
    Journal of Psychosocial Oncology 05/2015; 33(4). DOI:10.1080/07347332.2015.1046010
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    ABSTRACT: Objective: For people who are experiencing financial hardship, a cancer diagnosis can be devastating. For others, cancer may exacerbate financial stress, thereby influencing their livelihood, their ability to maintain employment benefits including health insurance, manage financial obligations, and participate meaningfully in cancer treatment. This study examined how vulnerabilities in psychosocial situations affect financial quality of life within the larger context of health-care decision making through a survey conducted with a cross-sectional availability sample of 90 cancer patients. Results from the multiple regression analysis found that health insurance adequacy, fewer perceived barriers to care, and reduced financial stress are significant predictors of better financial quality of life in this sample. Oncology social workers and other disciplines involved in psychosocial treatment with patients with cancer must assess and address financial and logistic aspects of life in order to provide comprehensive cancer care that meets all needs. Collaborative coordination with patients with cancer and their families to intervene psychosocially, medically, and financially are critical components of sound psychosocial and medical practice.
    Journal of Psychosocial Oncology 05/2015; 33(4). DOI:10.1080/07347332.2015.1045679
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    ABSTRACT: Young cancer patients are increasingly interested in preserving their fertility prior to undergoing gonadotoxic therapies. Although the medical safety and treatment protocols for fertility preservation have been well documented, limited research has addressed the emotional issues which arise in fertility preservation patients. We briefly review the literature on the psychosocial issues in adult female fertility preservation treatment and describe our experiences within this patient population patient. Our findings suggest that several important issues to be addressed during the psychological counseling of adult female fertility preservation patients include: 1) pre-existing psychological distress in patients undergoing treatment, 2) choice of fertility preservation strategy in the face of an uncertain relationship future, 3) decision making regarding use of third party reproduction (e.g., sperm/egg donation, gestational surrogacy), 4) treatment expectations regarding pregnancy and miscarriage, 5) ethical issues related to treatment including the creation, cryopreservation, and disposition of embryos/oocytes, and 6) decision regret from patients who declined fertility preservation.
    Journal of Psychosocial Oncology 05/2015; 33(4). DOI:10.1080/07347332.2015.1045677
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    ABSTRACT: Employment issues for cancer survivors (CS) were investigated from the perspective of Northern Ireland government general employment advisors. An e-survey was designed and developed based on the results of a scoping search of journal articles, previously validated questionnaires and relevant related surveys; discussions of draft versions of the e-survey and method with lead representatives of stakeholder organisations; and a pilot study with seven prospective respondents. The e-survey and subsequent reminder to employment advisors were distributed internally by the government employment advisory agency. The e-survey was completed by 78/156 (50%) advisors, the majority of whom (74%) received a request for advice in the last year from at least one CS. Most CS used the employment service less than one year (52%) or one year or more after treatment (32%). Fatigue was the most commonly reported barrier to returning to work (10%) and staying in work (14%); and a supportive employer was the top facilitating factor in returning to (21%), and continuing in (27%), employment. Although most advisors had a positive attitude about a CS's capacity to return-to-work, half were uncertain about how best to advise cancer survivors.
    Journal of Psychosocial Oncology 03/2015; 33(3). DOI:10.1080/07347332.2015.1019658
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    ABSTRACT: This study was conducted to identify the burden care and quality of life of caregivers of leukemia and lymphoma patients who had undergone peripheric stem cell transplantation. The sample consisted of 123 patient caregivers, all of whom were relatives. Data were collected using a survey, the Burden Interview, and the Caregiver Quality of Life Index Cancer Scale. Data evaluation was done using correlation analysis, Kruskall Wallis, and Mann-Whitney U tests. Factors that were significantly associated with quality of life and care burden perception included caring for an older patient, patient dependence for daily activities, and having low economic status.
    Journal of Psychosocial Oncology 03/2015; 33(3). DOI:10.1080/07347332.2015.1019660
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    ABSTRACT: Purpose. The goal of this study was to examine differences in physical functioning limitations among African-American and white breast cancer survivors. Methods. Data were analyzed from 724 African-American and 116 white breast cancer survivors who responded to a hospital registry-based survey. Physical functioning limitations were assessed using a series of eight questions in which individuals were asked about their ability to perform a physical task such as walking a quarter of a mile. A four category summary score, representing overall severity of limitation, was created using participant responses to the eight questions. Ordinal logistic regression was used to estimate the odds ratio (OR) and 95% confidence interval (CI) for the association between race and physical functioning limitation adjusted for potential confounders. Results. In the unadjusted model, the African-American breast cancer survivors were more than twice as likely to have a greater degree of physical functioning limitation compared to their white counterparts (OR 2.29; 95% CI 1.57, 3.34). After adjustment for covariates, including body mass index (BMI), the race OR was further attenuated and no longer statistically significant (OR 1.55; 95% CI 0.99, 2.44). Conclusions. Findings from this study showed that African-American breast cancer survivors were more likely to have worse physical functioning limitations than their white counterparts; however, much of this disparity was due to racial differences in other variables such as BMI. Future research should focus on effective interventions targeting modifiable risk factors of physical functioning limitations among breast cancer survivors with the goal of improving quality of life.
    Journal of Psychosocial Oncology 03/2015; 33(3). DOI:10.1080/07347332.2015.1019661