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Dive into the research topics where Helen M. Skerman is active.

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Featured researches published by Helen M. Skerman.


Journal of Clinical Oncology | 2005

Randomized Controlled Trial of an Educational Intervention for Managing Fatigue in Women Receiving Adjuvant Chemotherapy for Early-Stage Breast Cancer

Patsy Yates; Sanchia Aranda; Maryanne Hargraves; Bev Mirolo; Alexandra Clavarino; Sue-Anne McLachlan; Helen M. Skerman

PURPOSE To evaluate the efficacy of a psychoeducational intervention in improving cancer-related fatigue. PATIENTS AND METHODS This randomized controlled trial involved 109 women commencing adjuvant chemotherapy for stage I or II breast cancer in five chemotherapy treatment centers. Intervention group patients received an individualized fatigue education and support program delivered in the clinic and by phone over three 10- to 20-minute sessions 1 week apart. Instruments included a numeric rating scale assessing confidence with managing fatigue; 11-point numeric rating scales measuring fatigue at worst, average, and best; the Functional Assessment of Cancer Therapy-Fatigue and Piper Fatigue Scales; the Cancer Self-Efficacy Scale; the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire C30; and the Hospital Anxiety and Depression Scale. For each outcome, separate analyses of covariance of change scores between baseline (T1) and the three follow-up time points (T2, T3, and T4) were conducted, controlling for the variables corresponding baseline value. RESULTS Compared with the intervention group, mean difference scores between the baseline (T1) and immediate after the test (T2) assessments increased significantly more for the control group for worst and average fatigue, Functional Assessment of Cancer Therapy-Fatigue, and Piper fatigue severity and interference measures. These differences were not observed between baseline and T3 and T4 assessments. No significant differences were identified for any pre- or post-test change scores for confidence with managing fatigue, cancer self-efficacy, anxiety, depression, or quality of life. CONCLUSION Preparatory education and support has the potential to assist women to cope with cancer-related fatigue in the short term. However, further research is needed to identify ways to improve the potency and sustainability of psychoeducational interventions for managing cancer-related fatigue.


Research in Nursing & Health | 2009

Multivariate Methods to Identify Cancer-Related Symptom Clusters

Helen M. Skerman; Patsy Yates; Diana Battistutta

Multivariate methods are required to assess the interrelationships among multiple, concurrent symptoms. We examined the conceptual and contextual appropriateness of commonly used multivariate methods for cancer symptom cluster identification. From 178 publications identified in an online database search of Medline, CINAHL, and PsycINFO, limited to articles published in English, 10 years prior to March 2007, 13 cross-sectional studies met the inclusion criteria. Conceptually, common factor analysis (FA) and hierarchical cluster analysis (HCA) are appropriate for symptom cluster identification, not principal component analysis. As a basis for new directions in symptom management, FA methods are more appropriate than HCA. Principal axis factoring or maximum likelihood factoring, the scree plot, oblique rotation, and clinical interpretation are recommended approaches to symptom cluster identification.


BMC Cancer | 2013

Differences in the symptom experience of older versus younger oncology outpatients: a cross-sectional study

Janine K. Cataldo; Steven M. Paul; Bruce A. Cooper; Helen M. Skerman; Kimberly Alexander; Bradley E. Aouizerat; Virginia Schmied Blackman; John D. Merriman; Laura B. Dunn; Christine S. Ritchie; Patsy Yates; Christine Miaskowski

BackgroundMortality rates for cancer are decreasing in patients under 60 and increasing in those over 60 years of age. The reasons for these differences in mortality rates remain poorly understood. One explanation may be that older patients received substandard treatment because of concerns about adverse effects. Given the paucity of research on the multiple dimensions of the symptom experience in older oncology patients, the purpose of this study was to evaluate for differences in ratings of symptom occurrence, severity, frequency, and distress between younger (< 60 years) and older ( ≥ 60 years) adults undergoing cancer treatment. We hypothesized that older patients would have significantly lower ratings on four symptom dimensions.MethodsData from two studies in the United States and one study in Australia were combined to conduct this analysis. All three studies used the MSAS to evaluate the occurrence, severity, frequency, and distress of 32 symptoms.ResultsData from 593 oncology outpatients receiving active treatment for their cancer (i.e., 44.4% were < 60 years and 55.6% were ≥ 60 years of age) were evaluated. Of the 32 MSAS symptoms, after controlling for significant covariates, older patients reported significantly lower occurrence rates for 15 (46.9%) symptoms, lower severity ratings for 6 (18.9%) symptoms, lower frequency ratings for 4 (12.5%) symptoms, and lower distress ratings for 14 (43.8%) symptoms.ConclusionsThis study is the first to evaluate for differences in multiple dimensions of symptom experience in older oncology patients. For almost 50% of the MSAS symptoms, older patients reported significantly lower occurrence rates. While fewer age-related differences were found in ratings of symptom severity, frequency, and distress, a similar pattern was found across all three dimensions. Future research needs to focus on a detailed evaluation of patient and clinical characteristics (i.e., type and dose of treatment) that explain the differences in symptom experience identified in this study.


Climacteric | 2005

Associations between the use of complementary and alternative medications and demographic, health and lifestyle factors in mid-life Australian women

Sara Gollschewski; Debra Anderson; Helen M. Skerman; Philippa Lyons-Wall

Objective To determine the prevalence and types of complementary and alternative medications (CAMs) used by menopausal women living in South-East Queensland, Australia; and profile the women who are using CAMs through sociodemographic characteristics, self-rated health status, lifestyle and preventative health strategies. Method This study was a secondary data analysis of data collected by postal questionnaire from 886 women aged 48–67 years participating in the Queensland Midlife Womens Health Study. The outcome measure was CAM use, distinguished by three categories: herbal therapies, phytoestrogens and nutritional intake (supplements and healthy eating). Results The overall prevalence of CAM use among mid-life Australian women was 82% which included therapeutic techniques (83%), nutritional supplements (66.8%), phytoestrogens (55.8%), herbal therapies (41.3%), Evening Primrose oil (34%) and vitamin E (28.8%). CAM users, when compared to non-users, were more likely to be previous (p < 0.05) but not current users (p < 0.05) of hormone therapy (HT), higher educated (p < 0.05), low to middle income earners (p < 0.001) and have participated in self-breast examination (p < 0.01). They were also more likely to report good general health (p < 0.05) and improved physical functioning without limitations due to health (p < 0.05). CAM users were less likely to be aged over 55 years (p < 0.05) and smoke more than 20 cigarettes per day (p < 0.001). Conclusions/implications for health research As prevalence of current CAM use in this population group is considerably higher than HT use, health education programs to assist mid-life women to understand the scientific evidence (or lack of it) for their efficacy is recommended.


Journal of Pain and Symptom Management | 2015

Differences in Composition of Symptom Clusters Between Older and Younger Oncology Patients

Patsy Yates; Christine Miaskowski; Janine K. Cataldo; Steven M. Paul; Bruce A. Cooper; Kimberly Alexander; Bradley E. Aouizerat; Laura B. Dunn; Christine S. Ritchie; Alexandra L. McCarthy; Helen M. Skerman

CONTEXT Older oncology patients have unique needs associated with the many physical, psychological, and social changes associated with the aging process. The mechanisms underpinning and the impact of these changes are not well understood. Identification of clusters of symptoms is one approach that has been used to elicit hypotheses about the biological and/or psychological basis for variations in symptom experiences. OBJECTIVES The purposes of this study were to identify and compare symptom clusters in younger (<60 years) and older (≥60 years) patients undergoing cancer treatment. METHODS Symptom data from one Australian study and two U.S. studies were combined to conduct this analysis. A total of 593 patients receiving active treatment were dichotomized into younger (<60 years) and older (≥60 years) groups. Separate exploratory factor analyses (EFAs) were undertaken within each group to identify symptom clusters from occurrence ratings of the 32 symptoms assessed by the Memorial Symptom Assessment Scale. RESULTS In both groups, a seven-factor solution was selected. Four partially concordant symptom clusters emerged in both groups (i.e., mood/cognitive, malaise, body image, and genitourinary). In the older patients, the three unique clusters reflected physiological changes associated with aging, whereas in the younger group the three unique clusters reflected treatment-related effects. CONCLUSION The symptom clusters identified in older patients typically included a larger and more diverse range of physical and psychological symptoms. Differences also may be reflective of variations in treatment approaches between age groups. Findings highlight the need for better understanding of variation in treatment and symptom burden between younger and older adults with cancer.


Trials | 2014

The ENHANCES study—Enhancing Head and Neck Cancer patients’ Experiences of Survivorship: study protocol for a randomized controlled trial

Jane Turner; Patsy Yates; Lizbeth Kenny; Louisa Gordon; Bryan Burmeister; D. Thomson; Brett Hughes; Alexandra L. McCarthy; Chris Perry; Raymond Javan Chan; Alana Fraser; Helen M. Skerman; Martin D. Batstone; Kathryn Carswell

BackgroundFew cancers pose greater challenges than head and neck (H&N) cancer. Residual effects following treatment include body image changes, pain, fatigue and difficulties with appetite, swallowing and speech. Depression is a common comorbidity. There is limited evidence about ways to assist patients to achieve optimal adjustment after completion of treatment. In this study, we aim to examine the effectiveness and feasibility of a model of survivorship care to improve the quality of life of patients who have completed treatment for H&N cancer.Methods/DesignThis is a preliminary study in which 120 patients will be recruited. A prospective randomised controlled trial of the H&N Cancer Survivor Self-management Care Plan (HNCP) involving pre- and post-intervention assessments will be used. Consecutive patients who have completed a defined treatment protocol for H&N cancer will be recruited from two large cancer services and randomly allocated to one of three study arms: (1) usual care, (2) information in the form of a written resource or (3) the HNCP delivered by an oncology nurse who has participated in manual-based training and skill development in patient self-management support. The trained nurses will meet patients in a face-to-face interview lasting up to 60 minutes to develop an individualised HNCP, based on principles of chronic disease self-management. Participants will be assessed at baseline, 3 and 6 months. The primary outcome measure is quality of life. The secondary outcome measures include mood, self-efficacy and health-care utilisation. The feasibility of implementing this intervention in routine clinical care will be assessed through semistructured interviews with participating nurses, managers and administrators. Interviews with patients who received the HNCP will explore their perceptions of the HNCP, including factors that assisted them in achieving behavioural change.DiscussionIn this study, we aim to improve the quality of life of a patient population with unique needs by means of a tailored self-management care plan developed upon completion of treatment. Delivery of the intervention by trained oncology nurses is likely to be acceptable to patients and, if successful, will be a model of care that can be implemented for diverse patient populations.Trial registrationACTRN12613000542796 (registered on 15 May 2013)


Journal of Pain and Symptom Management | 2017

Symptom Clusters in Men With Castrate-Resistant Prostate Cancer

Petra Vayne-Bossert; Janet Hardy; Helen M. Skerman; Patsy Yates; Karyn Sullivan; Phillip Good

Men with metastatic castrate-resistant prostate cancer (CRPC) experience significant physical and mental health morbidity along with impaired quality of life (QoL).1 Pain related to skeletal metastases is the predominant physical symptom, but patients also suffer fatigue and drowsiness. On average, each prostate cancer patient has a median of four clinically relevant symptoms (defined as


Journal of Pain and Symptom Management | 2002

Barriers to Effective Cancer Pain Management: A Survey of Hospitalized Cancer Patients in Australia

Patsy Yates; Helen Edwards; Robyn Nash; Anne M. Walsh; Belinda J. Fentiman; Helen M. Skerman; Jake M. Najman

4/10 on the Edmonton Symptom Assessment Scale [ESAS]).2 Treatmentrelated symptoms may also occur, such as loss of libido, hot flashes, depression, osteoporosis, fatigue, weight gain, erectile dysfunction, and cognitive impairment with hormone suppression.


Patient Education and Counseling | 2004

A randomized controlled trial of a nurse-administered educational intervention for improving cancer pain management in ambulatory settings

Patsy Yates; Helen Edwards; Robyn Nash; Sanchia Aranda; David M. Purdie; Jake M. Najman; Helen M. Skerman; Anne M. Walsh


Nursing & Health Sciences | 2001

Determinants of nurses' intention to administer opioids for pain relief.

Helen Edwards; Robyn Nash; Jake M. Najman; Patsy Yates; Belinda J. Fentiman; Anne Dewar; Anne M. Walsh; Jan McDowell; Helen M. Skerman

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Patsy Yates

Queensland University of Technology

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Helen Edwards

Queensland University of Technology

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Robyn Nash

Queensland University of Technology

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Kimberly Alexander

Queensland University of Technology

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Steven M. Paul

University of California

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