5 results
Search Results
2. Theoretical and practical outline of the Copenhagen PACT narrative-based exercise counselling manual to promote physical activity in post-therapy cancer survivors.
- Author
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Midtgaard, Julie
- Subjects
TUMOR treatment ,CANCER patients ,CONCEPTUAL structures ,COUNSELING ,TUMORS ,SOCIAL support ,PHYSICAL activity ,DISEASE complications - Abstract
Background. Sedentary behaviour and reduced exercise capacity are potential persisting effects of anti-cancer therapy that may predispose to serious health conditions. It is well-established that physical exercise may prevent some of these problems. However, the extent to which cancer survivors are able to adopt long-term physical activity habits depends largely on their motivation. Aim. This theoretical paper aims to outline how researchers and practitioners can draw from Antonovsky's salutogenetic theory and White & Epston's Narrative Therapy to develop and implement intervention efforts centered on promotion of long-term physical activity behaviour, while at the same time increasing the individual cancer survivor's sense of meaning and personal health resources. Material and methods. The Copenhagen PACT (Physical Activity after Cancer Treatment) Study targeting adoption and maintenance of regular physical activity in post-therapy cancer survivors is briefly presented including a brief review of the theoretical rationale behind the psychological component of the intervention, i.e. a narrative-based exercise counselling programme. Subsequently, particular attention is given to the core principles, different components and structure of the counselling manual including sample questions and examples of written documents that have emanated from the individual counselling sessions. Discussion. The discussion includes consideration of some methodological challenges that arise when attempting to evaluate narrative-based interventions in the context of physical activity promotion in cancer rehabilitation and survivorship care. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
- View/download PDF
3. Prevalence and risk factors for sexual dysfunction in young women following a cancer diagnosis – a population-based study.
- Author
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Wettergren, Lena, Eriksson, Lars E., Bergström, Charlotta, Hedman, Christel, Ahlgren, Johan, Smedby, Karin E., Hellman, Kristina, Henriksson, Roger, and Lampic, Claudia
- Subjects
TUMOR treatment ,DYSPAREUNIA ,FEMALE reproductive organ diseases ,SEXUAL dysfunction ,MASTURBATION ,CROSS-sectional method ,HUMAN sexuality ,SEXUAL intercourse ,RISK assessment ,CANCER patients ,COMPARATIVE studies ,DISEASE prevalence ,DESCRIPTIVE statistics ,QUESTIONNAIRES ,TUMORS ,LOGISTIC regression analysis ,EMOTIONS ,HYPOACTIVE sexual desire disorder ,FEMALE reproductive organ tumors ,BREAST tumors ,PSYCHOLOGICAL distress ,BODY image ,DISEASE risk factors ,DISEASE complications ,ADULTS - Abstract
Self-reported sex problems among women diagnosed with reproductive and nonreproductive cancers before the age of 40 are not fully understood. This study aimed to determine sexual dysfunction in young women following a cancer diagnosis in relation to women of the general population. Furthermore, to identify factors associated with sexual dysfunction in women diagnosed with cancer. A population-based cross-sectional study with 694 young women was conducted 1.5 years after being diagnosed with cancer (response rate 72%). Potential participants were identified in national quality registries covering breast and gynecological cancer, lymphoma and brain tumors. The women with cancer were compared to a group of women drawn from the general population (N = 493). Sexual activity and function were assessed with the PROMIS® SexFS. Logistic regression was used to assess differences between women with cancer and the comparison group, and to identify factors associated with sexual dysfunction. The majority of the women with cancer (83%) as well as the women from the comparison group (87%) reported having had sex the last month (partner sex and/or masturbation). More than 60% of the women with cancer (all diagnoses) reported sexual dysfunction in at least one of the measured domains. The women with cancer reported statistically significantly more problems than women of the comparison group across domains such as decreased interest in having sex, and vaginal and vulvar discomfort. Women with gynecological or breast cancer and those receiving more intense treatment were at particular high risk of sexual dysfunction (≥2 domains). Concurrent emotional distress and body image disturbance were associated with more dysfunction. The results underscore the need to routinely assess sexual health in clinical care and follow-up. Based on the results, development of interventions to support women to cope with cancer-related sexual dysfunction is recommended. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
4. Decreasing access to cancer diagnosis and treatment during the COVID-19 pandemic in Poland.
- Author
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Maluchnik, Michał, Podwójcic, Krzysztof, and Więckowska, Barbara
- Subjects
TUMOR diagnosis ,TUMOR treatment ,CANCER patients ,CANCER patient medical care ,CHEST tumors ,HEALTH services accessibility ,LABOR incentives ,INDUSTRIAL safety ,PAY for performance ,PATIENT safety ,REGRESSION analysis ,RESPIRATORY organ tumors ,SMART cards ,TUMORS ,GASTROINTESTINAL tumors ,GOVERNMENT aid ,MALE reproductive organ cancer ,DATA analysis software ,DESCRIPTIVE statistics ,COVID-19 pandemic - Abstract
In the article, the authors present their study on the effects of the COVID-19 pandemic in the access to cancer diagnosis and treatment to oncological patients in Poland. Also cited are the use of the DiLO card to facilitate diagnosis and treatment in the country and the National Health Fund as the responsible party in paying hospitals for procedures on oncological patients.
- Published
- 2021
- Full Text
- View/download PDF
5. Managing the consequences of cancer treatment and the English National Cancer Survivorship Initiative.
- Author
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Maher, E. J.
- Subjects
TUMOR prevention ,TUMOR surgery ,TUMOR treatment ,CANCER chemotherapy ,CANCER patients ,RADIOTHERAPY ,TUMORS ,EVALUATION of human services programs - Abstract
Background. In 2007 the English National Cancer Survivorship initiative was launched as a partnership between a national charity, Macmillan Cancer Support, the English Department of Health (DH) and the quality improvement agency NHS Improvement. The initiative involved a number of work streams, one of which was to improve the detection and management of the Consequences of adult cancer Treatment (COT). Material and methods. The adult COT group took evidence from a range of stakeholders and published a vision and work programme focused on awareness raising, linking self- administered questionnaires to routine activity data collection and testing new models of care with a particular focus on pelvic cancers. Results. Key outputs include national media campaigns, publications demonstrating the value of linking cancer treatment episodes to routine recording of chronic illness, identification of sensitive Patient Reported Outcome Measures (PROMs) items for use in national surveys, evidence reviews and published national guidelines, together with the development of a three level risk stratified model of care. Pilot testing with survivors treated for pelvic cancers, and adult survivors with radiation-induced brachial plexopathy has been completed. Conclusion. Early results suggest that a systematic approach to the prevention, detection and management of some treatment-related consequences can significantly improve the ability of patients to manage their conditions. As a result of these findings, new services have now been commissioned by the NHS, initially for those with complex problems. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
- View/download PDF
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