8 results on '"Boltong, Anna"'
Search Results
2. A telephone outcall program to support caregivers of people diagnosed with cancer: utility, changes in levels of distress, and unmet needs
- Author
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Heckel, Leila, Fennell, Kate M., Orellana, Liliana, Boltong, Anna, Byrnes, Monica, and Livingston, Patricia M.
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- 2018
- Full Text
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3. A systematic review of cancer caregiver interventions: Appraising the potential for implementation of evidence into practice.
- Author
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Ugalde, Anna, Gaskin, Cadeyrn J., Rankin, Nicole M., Schofield, Penelope, Boltong, Anna, Aranda, Sanchia, Chambers, Suzanne, Krishnasamy, Meinir, and Livingston, Patricia M.
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META-analysis ,ELECTRONIC paper ,DATA extraction ,CANCER ,CAREGIVERS - Abstract
Objective: nformal caregivers provide substantial support for people living with cancer. Previous systematic reviews report on the efficacy of cancer caregiver interventions but not their potential to be implemented. The aim of this systematic review was to explore the potential for cancer caregiver interventions to be implemented into practice.Methods: We searched three electronic databases to identify cancer caregiver interventions on 5 January 2018. We operationalised six implementation outcomes (acceptability, adoption, appropriateness, feasibility, fidelity, and costs) into a tool to guide data extraction.Results: The search yielded 33 papers (27 papers from electronic databases and six papers from other sources) reporting on 26 studies that met review criteria. Fewer than half the studies (46%) contained evidence about the acceptability of interventions from caregivers' perspectives; only two studies (8%) included interventions developed with input from caregivers. Two studies (8%) addressed potential adoption of interventions, and no studies discussed intentions, agreement, or action to implement interventions into practice. All studies reported on intervention appropriateness by providing a rationale for the interventions. For feasibility, on average less than one-third of caregivers who were eligible to be involved consented to participate. On fidelity, whether interventions were conducted as intended was reported in 62% of studies. Cost data were reported in terms of intervention delivery, requiring a median time commitment of staff of 180 minutes to be delivered.Conclusions: Caregiver intervention studies lack components of study design and reporting that could bridge the gap between research and practice. There is enormous potential for improvements in cancer caregiver intervention study design to plan for future implementation. [ABSTRACT FROM AUTHOR]- Published
- 2019
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4. Exploring the rationale, experience and impact of using Cancer Information and Support (CIS) services: an international qualitative study.
- Author
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Boltong, Anna, Ledwick, Martin, Babb, Kevin, Sutton, Clare, and Ugalde, Anna
- Subjects
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SUPPORT groups for cancer patients , *INFORMATION storage & retrieval systems , *CANCER information services , *CANCER treatment , *HEALTH care teams , *ONCOLOGY nursing , *ONCOLOGY - Abstract
Purpose: The aim of this study was to develop an in-depth understanding of the rationale, experiences, evaluation and outcomes of using Cancer Information and Support (CIS) services in Australia, the UK and USA. Methods: Semi-structured interviews were used to gather data between November 2015 and January 2016. Telephone interviews were recorded, de-identified, transcribed and thematically analysed. Ten users from each of three international CIS services ( n = 30 in total) were recruited. Participants were eligible for inclusion if they had utilised the CIS in 2015 via telephone contact with a cancer nurse and identified as a patient or cancer survivor, or friend or family member of such a person. Results: Four major themes were derived and included a total of 25 sub-themes. Key themes included (i) drivers for access, (ii) experience of the service, (iii) impact and (iv) an adjunct to cancer treatment services. Conclusions: Cancer Information and Support nurses internationally act as expert navigators, educators and compassionate communicators who 'listen between the lines' to enable callers to better understand and contextualise their situation and discuss it with their healthcare team and family and friends. Use of the service can result in reduced worry, extend support repertoires and enable use of new knowledge and language as a tool to getting the most from the healthcare team. The positioning of CIS alongside cancer treatment services aids fuller integration of supportive care, benefiting both patients and clinicians. [ABSTRACT FROM AUTHOR]
- Published
- 2017
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5. A Prospective Cohort Study of the Effects of Adjuvant Breast Cancer Chemotherapy on Taste Function, Food Liking, Appetite and Associated Nutritional Outcomes.
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Boltong, Anna, Aranda, Sanchia, Keast, Russell, Wynne, Rochelle, Francis, Prudence A., Chirgwin, Jacqueline, and Gough, Karla
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LONGITUDINAL method , *COHORT analysis , *TASTE , *APPETITE , *HEALTH outcome assessment ,BREAST cancer chemotherapy - Abstract
Background: ‘Taste’ changes are commonly reported during chemotherapy. It is unclear to what extent this relates to actual changes in taste function or to changes in appetite and food liking and how these changes affect dietary intake and nutritional status. Patients and methods: This prospective, repeated measures cohort study recruited participants from three oncology clinics. Women (n = 52) prescribed adjuvant chemotherapy underwent standardised testing of taste perception, appetite and food liking at six time points to measure change from baseline. Associations between taste and hedonic changes and nutritional outcomes were examined. Results: Taste function was significantly reduced early in chemotherapy cycles (p<0.05) but showed recovery by late in the cycle. Ability to correctly identify salty, sour and umami tastants was reduced. Liking of sweet food decreased early and mid-cycle (p<0.01) but not late cycle. Liking of savory food was not significantly affected. Appetite decreased early in the cycle (p<0.001). Reduced taste function was associated with lowest kilojoule intake (r = 0.31; p = 0.008) as was appetite loss with reduced kilojoule (r = 0.34; p = 0.002) and protein intake (r = 0.36; p = 0.001) early in the third chemotherapy cycle. Decreased appetite early in the third and final chemotherapy cycles was associated with a decline in BMI (p = <0.0005) over the study period. Resolution of taste function, food liking and appetite was observed 8 weeks after chemotherapy completion. There was no association between taste change and dry mouth, oral mucositis or nausea. Conclusion: The results reveal, for the first time, the cyclical yet transient effects of adjuvant chemotherapy on taste function and the link between taste and hedonic changes, dietary intake and nutritional outcomes. The results should be used to inform reliable pre-chemotherapy education. [ABSTRACT FROM AUTHOR]
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- 2014
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6. Chemosensory Changes from Cancer Treatment and Their Effects on Patients' Food Behavior: A Scoping Review.
- Author
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Nolden, Alissa A., Hwang, Liang-Dar, Boltong, Anna, and Reed, Danielle R.
- Abstract
Individuals undergoing treatment for cancer can experience changes in taste or smell that are often assumed to affect constructs related to food behavior, although this relationship is rarely measured directly. To ascertain the extent to which measured changes in taste and smell during and after cancer treatment affect food behavior, we conducted a scoping review and completed a comparative analysis for studies that met our criteria, which were: they directly measured cancer patients' (a) psychophysical response to taste and/or olfactory stimuli, and (b) food behavior (including food enjoyment, food preference, dietary intake) in people affected by cancer. Eleven studies met these criteria and were included in the review. All 11 studies evaluated taste and five also measured smell. A comparative analysis exploring taste and food behavior shows that a reduced sweet taste function (decreased sensitivity) was associated with a reduced intake of a variety of different macro and micro nutrients, reduced appetite, and overall lower energy intake. One out of six studies that measured smell and food measured observed changes in olfactory function following cancer treatment. There were no significant relationships reported between olfactory measures and food behavior. Taste changes that arise from cancer treatment appear to have a direct effect on food behavior, although there is a need for more research using standardized measures and larger sample sizes. A better understanding of taste alterations and their implications for dietary intake and food enjoyment will support optimal nutritional health by identifying strategies to help patients eat well during and after cancer treatment. [ABSTRACT FROM AUTHOR]
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- 2019
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7. A telephone outcall program to support caregivers of people diagnosed with cancer: utility, changes in levels of distress, and unmet needs
- Author
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Monica Byrnes, Anna Boltong, Patricia M. Livingston, Leila Heckel, Kate M. Fennell, Liliana Orellana, Heckel, Leila, Fennell, Kate M, Orellana, Liliana, Boltong, Anna, Byrnes, Monica, and Livingston, Patricia M
- Subjects
Adult ,Male ,caregivers ,medicine.medical_specialty ,Pain medicine ,Burnout, Psychological ,Unmet needs ,03 medical and health sciences ,0302 clinical medicine ,telephone intervention ,Hotlines ,Neoplasms ,Surveys and Questionnaires ,medicine ,cancer ,Humans ,030212 general & internal medicine ,Aged ,business.industry ,Nursing research ,distress ,unmet ,Social Support ,Cancer ,Middle Aged ,medicine.disease ,Telephone ,Distress ,Caregivers ,Oncology ,030220 oncology & carcinogenesis ,Family medicine ,oncology ,Female ,business ,Needs Assessment ,Stress, Psychological ,Follow-Up Studies - Abstract
Purpose: To evaluate the utility of a telephone outcall program for cancer caregivers and to examine longitudinal changes in their distress levels and supportive care needs. Methods: As part of the PROTECT trial, caregivers assigned to the intervention arm (N = 108) received three telephone outcalls from a Cancer Council 13 11 20 nurse at three time points (7–10 days post-randomization, 1 and 4 months later). During each call, caregivers were screened for distress using the Distress Thermometer (range: 0–10) then six supportive care issues were raised for discussion. Participants completed a utility survey 1 month post-intervention. Results: The outcall program was highly acceptable and perceived as beneficial by caregivers. Overall, 95% reported it was worth their time to take part in the outcall program and 82% stated that the program was very relevant to them. Level of distress and impact of distress decreased over time (p = 0.0031, p < 0.0001, respectively). Average call duration decreased over time (p < 0.0001) and was longer for female than male caregivers (p = 0.0009). The frequency of caregivers discussing issues related to psychological distress (p = 0.0003), health literacy (p < 0.0001), financial (p = 0.0014), and practical concerns (p = 0.0121) decreased over time. Psychological distress was more often discussed by female than male caregivers (p = 0.0153), and family issues more often by younger (< 55 years) than older caregivers (p = 0.0071). Conclusions: Utility of this outcall program was high. Caregivers’ level of distress and unmet needs decreased over time. Gender and age differences emerged, which warrants the need for tailored support. Further research is necessary to identify the best method of improving access to 13 11 20 services for caregivers Refereed/Peer-reviewed
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- 2018
8. Efficacy of a telephone outcall program to reduce caregiver burden among caregivers of cancer patients [PROTECT]: a randomised controlled trial
- Author
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Melinda Williams, Mari Botti, Kate M. Fennell, John V. Reynolds, Cadeyrn J. Gaskin, Cathrine Mihalopoulos, Anna Boltong, Jacquie Chirgwin, David M. Ashley, Patricia M. Livingston, Richard H. Osborne, Leila Heckel, Heckel, Leila, Fennell, Kate M, Reynolds, John, Boltong, Anna, Botti, Mari, Osborne, Richard H, Mihalopoulos, Cathrine, Chirgwin, Jacquie, Williams, Melinda, Gaskin, Cadeyrn J, Ashley, David M, and Livingston, Patricia M
- Subjects
Male ,Cancer Research ,Psychological intervention ,law.invention ,0302 clinical medicine ,Quality of life ,Randomized controlled trial ,law ,Neoplasms ,Adaptation, Psychological ,Health care ,Single-Blind Method ,030212 general & internal medicine ,Helpline ,Cancer ,support ,Depression ,Telephone intervention ,Caregiver burden ,Middle Aged ,lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,3. Good health ,Oncology ,Caregivers ,030220 oncology & carcinogenesis ,depression ,Female ,Support ,RCT ,Research Article ,Adult ,caregivers ,medicine.medical_specialty ,unmet needs ,Health literacy ,lcsh:RC254-282 ,Unmet needs ,03 medical and health sciences ,telephone intervention ,Intervention (counseling) ,helpline ,Genetics ,medicine ,Humans ,cancer ,Aged ,caregiver burden ,business.industry ,Telephone ,Clinical trial ,Family medicine ,Quality of Life ,business ,health literacy - Abstract
Background Informal caregivers provide extended support to people with cancer but they receive little support from the health care system to assist them in their caring role. The aim of this single-blind, multi-centre, randomised controlled trial was to test the efficacy of a telephone outcall program to reduce caregiver burden and unmet needs, and improve psychological well-being among cancer caregivers, as well as evaluating the potential impact on patient outcomes. Methods Cancer patient/caregiver dyads (N = 216) were randomised to a telephone outcall program (n = 108) or attention control group (n = 108). The primary outcome was self-reported caregiver burden. Secondary endpoints included depressive symptoms, unmet needs, self-esteem, self-empowerment, and health literacy. Data were collected at baseline and at both 1 and 6 months post-intervention. An intention to treat analysis was performed. Results The intervention had no effect on the primary outcome (caregiver burden), but reduced the number of caregiver unmet needs (intervention group baseline, mean = 2.66, 95% confidence interval (CI) [1.91–3.54]; intervention group 1 month post intervention, mean = 0.85, 95%CI [0.42–1.44]; control group baseline, mean = 1.30 95%CI [0.80–1.94], control group 1 month post intervention, mean = 1.02 95%CI [0.52–1.69]; p = 0.023). For caregivers at risk for depression, the intervention had a significant effect on caregivers’ confidence in having sufficient information to manage their health (p = 0.040). No effects were found for patients’ depressive symptoms, unmet needs, self-empowerment, and other health literacy domains. Conclusions While caregiver burden was not reduced, the outcall program was effective in reducing unmet needs in caregivers. Provision of cancer information and support via a telephone service may represent a feasible approach to reducing unmet needs among cancer caregiver populations. Trial registration ACTRN12613000731796; prospectively registered on 02/07/2013. Electronic supplementary material The online version of this article (10.1186/s12885-017-3961-6) contains supplementary material, which is available to authorized users.
- Published
- 2018
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