Good death among elderly cancer patients in Japan based on perspectives of the general population (#401)
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Smoking behaviour of students in the University of Ibadan, Nigeria (#402)
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Distress in patients and their natural caregivers early after the diagnosis of inoperable lung cancer (#403)
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Psychosexual effects of gynaecological cancer survivors in India (#404)
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Prostate cancer – men aren’t the only ones (#405)
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Integration of the health team to address the patients’ emotional aspects: Caring for the whole patient (#406)
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Reports from patients with advanced cancer and their caregivers of their health related quality of life (HRQoL). (#407)
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Posttraumatic growth in adult cancer survivors: a critical review of empirical research using the organismic valuing theory of growth (#408)
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Mental disorders in people diagnosed with cancer: Findings from the 2007 Australian National Survey of Mental Health and Wellbeing (#409)
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Stressful events and coping strategies among postmenopausal women during active treatment for primary or recurrent breast cancer. (#410)
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Employee to employer communication skills: Balancing cancer treatment and employment (#411)
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African American cancer patients’ perceptions of participation in a phase I,II, or III clinical trial: What do refusers say? (#412)
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Cognitive performance and psychosocial well-being of cancer patients: A preliminary study (#413)
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Chinese breast cancer patients undergoing radiotherapy: role of fatigue and its influences on their quality of life (#414)
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Predictors of engagement in an online psychological support program for men treated for prostate cancer (#415)
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Using the distress thermometer and the hospital anxiety and depression scale in Italian women newly diagnosed with breast cancer (#416)
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The implementation of a mindfulness group programme throughout the state of Queensland (#417)
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Intentions to use telephone and face-to-face support services: Attitudes of Australian men following prostatectomy. (#418)
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Patient preferences for adjuvant radiotherapy in early breast cancer – an Australian sub-study of the International TARGIT trial. (#419)
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Informational needs and deficits of Latinas diagnosed with breast cancer (#420)
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Demographic factors, referral patterns and clinical correlates in Adjustment Disorder in cancer patient referrals to an in-house liaison psychiatry service in a tertiary care oncology hospital in India (#422)
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Evaluation of a training module on client centered counseling in cancer conducted for volunteers working in oncology in a tertiary care cancer hospital in India (#424)
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Does it do what it says on the tin? : An evaluation of using a licensed communication skills training product within a regional education strategy to increase capability and capacity in end of life care (#426)
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“It’s a very difficult balance”: A qualitative study of cancer specialists’ perceptions of discussing Complementary and Alternative Medicine with their patients (#427)
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Association among depression, demoralization, and posttraumatic growth in cancer patient: preliminary study (#428)
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The physician-patient relationship and the experience of pain: A study of women undergoing diagnostic mammography (#429)
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"What should be taught to future clinicians and health-care professionals regarding grief reactions in the cancer field?" (#430)
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Current definitions and measures of quality of life in pediatric palliative care: A systematic review (#431)
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A systematic review comparing quality of life definitions and measurement strategies between adult palliative care and pediatric palliative care (#432)
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Daily bad news in stage IV cancer inpatients (#433)
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Lessons learnt from setting up a multi-centre cohort study in the UK: A cohort study to explore recovery of health and well-being following primary treatment of colo-rectal cancer (CREW (ColoRectal Wellbeing) cohort). (#434)
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Why don’t people get screened for cancer? Preliminary results from an online survey reaching under and never screened populations (#435)
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Implementing a national strategy for achieving person-centered care: the need for multiple strategies (#436)
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Effects of family therapy on the communication of patient suffering from cancer and its family. (#437)
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An exploratory study on factors associated with patient preferences for communication (#438)
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Hope & Hurdles: An information resource for women with secondary breast cancer (#439)
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Applying an evidence-based approach to development and evaluation of resources for families facing advanced cancer: Lessons learned from the “Consumer Toolkit” (#440)
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“I know you think there is this system: but this is what actually happened to me?” Translating cancer research into a responsive supportive care system of services, programs and policies. (#441)
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Cancer patients’ opinions of psychosocial screening. (#442)
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“Where now?” – Pilot study of a course for people living beyond cancer (#443)
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Are there differences between the written and the oral means of screening psychosocial distress with the Distress Thermometer in cancer patients? (#444)
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The bidirectional relationships of coping strategies and distress: a study among Taiwanese newly-diagnosed breast cancer patients. (#445)
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Developing a nationally collaborative framework for psychosocial oncology research: a review of the UK NCRI psychosocial oncology clinical studies group. (#446)
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Spirituality and meaning in life of the Japanese female breast cancer patients (#447)
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Depression predicts lower use of services in gynaecological cancer survivors (#448)
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A randomized, controlled trial of meditation for women with breast cancer (#449)
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‘Living beneath the sword of Damocles’: Perceptions of risk and fears of cancer recurrence amongst Australian melanoma survivors at high or moderate risk of developing new primary disease. (#450)
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"The critical ingredients of success": Evaluation findings of a supervised exercise programme for men who have had a diagnosis of cancer. (#451)
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Psychosocial impact of a cancer diagnosis on patients and families in Subsaharan Africa. (#452)
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Men with cancer using Complementary and Alternative Medicine (CAM): variations in significant others’ involvement (#453)
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Attitude to psycho-oncology and palliative care in Serbia today (descriptive presentation) (#454)
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Psychological support for parents, teens and adolescents during the treatment when a child or teen dies at the Oncological department (#455)
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Population survey on Swedish women’s attitudes towards tailored mammography screening based on individual risk for breast cancer (#456)
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Are caregivers of cancer patients depressed? - A single centre experience from South India. (#457)
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Factors influencing the treatment choices in early stage newly diagnosed carcinoma cervix patients - a single centre experience from South India. (#458)
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Targets for psychosocial treatment: family and work after breast cancer (#459)
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Couples coping with cancer: A qualitative study of the views of health care providers (#460)
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Exploration of the experiences and decision making of older people with cancer. (#461)
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Transition to follow-up care after breast cancer treatment in rural Australia: Women’s experiences of service provision (#462)
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A cognitive behavioural intervention on biopsychosocial factors in patients with cancer fatigue - A comparative, correlational study. (#463)
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Quality of life, posttraumatic stress and posttraumatic growth in breast cancer survivors (#464)
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The epidemiology of psychiatric disorders among women with breast cancer in South Korea: analysis of the national registry data (#465)
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Pre & post effects of the community support services on the QOL of cancer patients in Hong Kong (#466)
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Benefit finding in parental cancer: Prevalence, types and predictors (#467)
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Posttraumatic growth levels and their influencing factors among Chinese breast cancer patients (#468)
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Complementary and alternative medicine use of women with breast cancer: Self-help CAM attracts other women than guided CAM therapies (#469)
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Arthralgia with aromatase inhibitors: association with quality of life, emotional state and fear of recurrence (#470)
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Anxiety and depression during radiotherapy treatment: A comparison of touchscreen computer administration of the Hospital Anxiety and Depression Scale and single-item self-report measures (#471)
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Establishing a multidisciplinary service, The Hunter & Northern NSW Youth Cancer Service, Australia (#472)
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Adolescent and Young Adult (AYA) Task Force: identifying and evaluating educational and psychosocial needs of AYA’s. (#473)
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The importance of health literacy to adolescent and young adult cancer patients (#474)
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Ovarian cancer patients’ expectations of palliative chemotherapy: the fine line between hope and misunderstanding (#475)
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The lived experience of breast cancer survivors participating in challenge-based peer support programs: The transformative effect of riding motorcycles (#476)
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Need for psychosocial care – expressed by patients in primary treatment (#477)
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Prevalence of ‘Problem List’ symptoms among oncology outpatients and relationship with distress. (#479)
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Psychosocial concerns and coping strategies of patients with advanced stage Hepatobiliary cancer (#480)
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The effect of a specific music therapy song writing protocol on adult cancer patients mood - a mixed method, multi-site, randomized, wait-list controlled trial (#481)
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Identifying emotion in text generated from online interventions for people who have survived cancer (#482)
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Early palliative care improves the prognosis of cancer patients (#483)
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Posttraumatic stress symptoms as an important reaction in children who donate their stem cell to their siblings with cancer (#484)
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Posttraumatic stress symptoms among parents of childhood cancer in transition from inpatient to outpatient settings. (#485)
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Comparison of quality of life between cancer survivors and people with chronic stable diseases (#486)
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From a distance: the influence of dispositions and self-distanced analyses on affect among parents of pediatric cancer patients (#487)
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What happens online? Pilot evaluation of how breast cancer survivors use the non-guided Internet-based self-management intervention BREATH. (#488)
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My Changed Body: Breast cancer, body image, distress and self-compassion (#489)
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Avoidance of disgust's elicitors in colorectal contexts: mindfulness predicts avoidance when avoidance makes sense (#490)
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Factors influencing primary care physicians’ decision to order prostate-specific antigen (PSA) test for healthy men (#491)
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The effects of rumination on illness-related future thinking in young people: Implications for promoting resilience after cancer (#492)
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Resilience in cancer survivors after allogeneic hematopoietic stem cell transplantation (#493)
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Correlates of post-traumatic stress disorder (PTSD) and post-traumatic growth (PTG) in oncology populations: A systematic review and meta-analysis. (#494)
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Supporting Men, Supporting Women: Development of a web-based information and support resource for support partners of women undergoing genetic testing for breast cancer risk (#495)
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Clinical bio-psycho-social risk factors for depression in lung cancer patients: a comprehensive analysis using data from the Lung Cancer Database Project (#496)
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Comparison between patients with hepatitis c and hepatocellular carcinoma in quality of life and its related factors during receiving treatment (#497)
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“There is no information for us” - the development of the first Victorian gay men’s prostate Cancer Support Group. (#498)
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The use of a Personality/Stress Questionnaire in the prediction of cancer or CHD in healthy probands (#499)
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Experience of death conference at general hospital setting in Japan (#500)
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Associations between depressive mood, health behaviour, and diurnal cortisol slopes among women with breast cancer (#503)
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A systematic review of the recent quality of life studies in adult extremity sarcoma survivors: Need for further research to assess role of psychological distress in influencing overall outcomes (#504)
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Fear of cancer recurrence in young breast cancer survivors: the role of meta-cognitive style and disease-related factors. (#505)
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Intrusive thoughts after prostate cancer diagnosis and surgery (#506)
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Thinking about one’s own death when diagnosed with prostate cancer. (#507)
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Cancer patients’ rehabilitation in Europe: results from the Eurochip-3 project (#508)
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Breast cancer meanings: a cognitive-developmental study (#509)
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Sense-of-Coherence in breast cancer: is it protective of psychological morbidity? (#510)
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Expected friends reactions to cancer disclosure: an exploratory vignettes study among Japanese cancer survivors (#511)
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Building a psyco-oncology unit at a cancer center. Is this really one of the ways to break the stigma related to psychiatric care among cancer patients? (#512)
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Research informing practice: How can we translate hope in the palliative care practice? (#513)
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Follow-up contacts with the psychosocial care team after screening for distress in newly diagnosed cancer patients (#514)
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Testing reciprocal relationships between coping and post-traumatic growth among breast cancer patients: a cross-lagged structural equation study of approach, emotional, and disengage coping. (#515)
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Spiritual wellbeing in caregivers of geriatric cancer survivors: the association of peace, meaning, and faith to psychological morbidity and resilience (#517)
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The impact of cancer on development in adolescent and young adults: Perspectives from patients and health professionals. (#518)
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Death anxiety reduction after attending the psychological group tackling spiritual concerns (#519)
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My Choice, My Voice: End of life planning with adolescents and young adults (#520)
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Depression and anxiety in breast cancer patients undergoing chemotherapy (#521)
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