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Madeleine King

Biographic Data

ID3929588
NAMEMadeleine King
GIVEN NAMESMadeleine
FAMILY NAMEKing
SIGNATUREKING M
AFFILIATIONSThe University of Sydney
ORCID0000-0001-7192-2887
VERIFIEDYes
TOTAL WORKS45
TOTAL CITATIONS22
AUTHOR COUNT45
EDITOR COUNT0
FIRST PUBLICATION YEAR1991
LATEST PUBLICATION YEAR2024
H-INDEX2
  • Japanese value set for the EORTC QLU-C10D

    Open Access•Takeru Shiroiwa, Madeleine King et al.•ARTICLE•Quality of Life Research•2024

    The Japan-specific QLU-C10D value set is suitable for evaluating the cost and utility of oncology treatments for Japanese health technology assessment and decision-making

  • Danish value sets for the EORTC QLU-C10D utility instrument

    Open Access•Jens Lehmann, Leslye Rojas-Concha et al.•ARTICLE•Quality of Life Research•2024

    The EORTC QLU-C10D is a relatively new multi-attribute utility instrument and is a promising cancer-specific health technology assessment candidate measure. The country-specific Danish utility weights from this study can be used for cost-utility analyses in Danish patients and for comparison with other country-specific utility data

  • Relationship between reasons for intermittent missing patient-reported outcomes data and missing data mechanisms

    Open Access•Lene Kongsgaard Nielsen, Rebecca Mercieca‐Bebber et al.•ARTICLE•Quality of Life Research•2024

    Intermittent NRs due to hospital admission, mental or physical reasons were aligned with MNAR mechanism for nearly half of PRO domains, while intermittent NRs due to technical difficulties/procedural errors or other/unspecified reasons generally were aligned with MCAR mechanism

  • Norwegian and Swedish value sets for the EORTC QLU-C10D utility instrument

    Open Access•Gudrun Rohde, Jens Lehmann et al.•ARTICLE•Quality of Life Research•2024

    This study provides the first set of utility weights for the EORTC QLU-C10D specific to Norway and Sweden, reflecting the unique health preferences of these populations. The generated utility decrements can inform cost-utility analyses and optimize resource allocation in cancer care within the Norwegian and Swedish healthcare systems

  • Chinese utility weights for the EORTC cancer-specific utility instrument QLU-C10D

    Open Access•Yiyin Cao, Juan Xu et al.•ARTICLE•Quality of Life Research•2024

  • Th Annual Conference of the International Society for Quality of Life Research

    Open Access•Lene id_orcid 0000-0003- Kongsgaard Nielsen, Soren id_orcid Moller et al.•ARTICLE•Quality of Life Research•2023

  • Apples to apples? Comparison of the measurement properties of hospital anxiety and depression-anxiety subscale (Hads-A), depression, anxiety and stress scale-anxiety subscale (Dass-A), and generalised…

    Open Access•Kerrie Clover, Sylvie D Lambert et al.•ARTICLE•Current Psychology•2022

  • Health-related quality of life of Australians during the 2020 Covid-19 pandemic

    Open Access•Rebecca Mercieca‐Bebber, Rachel Campbell et al.•ARTICLE•Quality of Life Research•2022

    ANZCTR number is: ACTRN12621001240831. Web address of your trial: https://www.anzctr.org.au/ACTRN12621001240831.aspx . Date submitted: 26/08/2021 2:56:53 PM. Date registered: 14/09/2021 9:40:31 AM. Registered by: Margaret-Ann Tait. Principal Investigator: Madeleine King

  • Improving the patient-reported outcome sections of clinical trial protocols

    Open Access•Madeleine King, Margaret-Ann Tait et al.•ARTICLE•Quality of Life Research•2022

    Although participants were highly satisfied with these workshops, the completeness of PRO protocol content generally did not improve. Additional knowledge translation efforts are needed to assist protocol writers address SPIRIT-PRO guidance and avoid research waste that may eventuate from sub-optimal PRO protocol content

  • Th Annual Conference of the International Society for Quality of Life Research

    Open Access•Lene id_orcid 0000-0003- Nielsen, Lene Kongsgaard Nielsen et al.•ARTICLE•Quality of Life Research•2021

  • EORTC QLU-C10D value sets for Austria, Italy, and Poland

    Open Access•Eva‐Maria Gamper, MT King et al.•ARTICLE•Quality of Life Research•2020

    QLU-C10D cancer-specific utilities can now be calculated in three more countries. Differences between countries indicate that careful consideration is required when using non-country-specific value sets in economic evaluations

  • Strategies to improve patient-reported outcome completion rates in longitudinal studies

    Open Access•Lene Kongsgaard Nielsen, Madeleine King et al.•ARTICLE•Quality of Life Research•2019

    Electronic reminders and real-time monitoring contributed to a very high completion rate in the study. To increase the quality of PRO data, we propose integrating these strategies in PRO studies, however highlighting that an increase in staff resources is required for implementation

  • German value sets for the EORTC QLU-C10D, a cancer-specific utility instrument based on the EORTC QLQ-C30

    Open Access•Georg Kemmler, Eva‐Maria Gamper et al.•ARTICLE•Quality of Life Research•2019

    This study established German utility weights for the cancer-specific utility instrument QLU-C10D

  • Can Methods Developed for Interpreting Group-level Patient-reported Outcome Data be Applied to Individual Patient Management

    Madeleine King, Madeleine T King et al.•ARTICLE•Medical Care•2019•References: 38

    BACKGROUND: Patient-reported outcome (PRO) data may be used at 2 levels: to evaluate impacts of disease and treatment aggregated across individuals (group-level) and to screen/monitor individual patients to inform their management (individual-level). For PRO data to be useful at either level, we need to understand their clinical relevance. PURPOSE: To provide clarity on whether and how methods historically developed to interpret group-based PRO r…

  • Trials with patient-reported outcomes registered on the Australian New Zealand Clinical Trials Registry (ANZCTR)

    Open Access•the International Society for Quality of Life Research, Rebecca…•ARTICLE•Quality of Life Research•2018

  • PROMIS depression measures perform similarly to legacy measures relative to a structured diagnostic interview for depression in cancer patients

    Open Access•Kerrie Clover, Sylvie D Lambert et al.•ARTICLE•Quality of Life Research•2018

  • Preliminary evidence on the uptake, use and benefits of the Consort-PRO extension

    Open Access•Rebecca Mercieca‐Bebber, Julie Rouette et al.•ARTICLE•Quality of Life Research•2017

  • Measuring what matters Most

    Open Access•Madeleine King, Madeleine T King et al.•ARTICLE•Quality of Life Research•2017

  • Qlu-C10d

    Open Access•Madeleine King, M T King et al.•ARTICLE•Quality of Life Research•2016

  • Phase 1 in the development of a patient-reported measure to quantify perceived inconvenience of radiotherapy

    Open Access•Puma Sundaresan, Christopher Milross et al.•ARTICLE•Quality of Life Research•2016

  • The Impact of Cancer on Psychological and Social Outcomes

    Open Access•Daniel Costa, Daniel Sj Costa et al.•ARTICLE•Australian Psychologist•2016•Cited by: 1•References: 4

    Cancer is now the biggest cause of mortality worldwide. Although the debilitating physical symptoms of cancer have long been known, the psychological and social impacts of cancer have become the subject of examination only relatively recently. The psychological outcomes that have been examined are primarily negative emotional variables, e.g., anxiety, but emerging research has focused on positive emotional variables, e.g., post‐traumatic growth, …

  • International Society for Quality of Life Research commentary on the draft European Medicines Agency reflection paper on the use of patient-reported outcome (PRO) measures in oncology studies

    Open Access•Derek Kyte, Bryce B Reeve et al.•ARTICLE•Quality of Life Research•2015

  • Using a discrete choice experiment to value the QLU-C10D

    Open Access•Richard Norman, Rowena Viney et al.•ARTICLE•Quality of Life Research•2015

  • Bias in Area Under the Curve for Longitudinal Clinical Trials With Missing Patient Reported Outcome Data

    Open Access•Melanie L Bell, Madeleine King et al.•ARTICLE•SAGE Open•2014

    A common approach to the analysis of longitudinal patient reported outcomes (PROs) is the use of summary measures such as area under the time curve (AUC). However, it is not clear how missing data affects the validity of AUC analysis. This study aimed to compare the use of AUC summary measures (in individuals) with AUC summary statistics (on groups, calculated from the estimated parameters of a mixed model) when data are complete, missing at rand…

  • Testing the measurement invariance of the EORTC QLQ-C30 across primary cancer sites using multi-group confirmatory factor analysis

    Open Access•Daniel Costa, D S J Costa et al.•ARTICLE•Quality of Life Research•2014

Next
  • Is general practitioner decision making associated with patient socio-economic status

    Open Access•Anthony Scott, Alan Shiell et al.•ARTICLE•Social Science & Medicine•1996•Cited by: 12•References: 41

  • The physical functioning and mental health of informal carers

    Open Access•Patricia Kenny, Madeleine King et al.•ARTICLE•Health & Social Care in the…•2014•Cited by: 9•References: 3

    Informal carers represent a substantial proportion of the population in many countries and health is an important factor in their capacity to continue care-giving. This study investigated the impact of care-giving on the mental and physical health of informal carers, taking account of contextual factors, including family and work. We examined health changes from before care-giving commenced to 2 and 4 years after, using longitudinal data from the…

  • The Impact of Cancer on Psychological and Social Outcomes

    Open Access•Daniel Costa, Daniel Sj Costa et al.•ARTICLE•Australian Psychologist•2016•Cited by: 1•References: 4

    Cancer is now the biggest cause of mortality worldwide. Although the debilitating physical symptoms of cancer have long been known, the psychological and social impacts of cancer have become the subject of examination only relatively recently. The psychological outcomes that have been examined are primarily negative emotional variables, e.g., anxiety, but emerging research has focused on positive emotional variables, e.g., post‐traumatic growth, …

  • Le cercle de généalogie juive

    Madeleine King•ARTICLE•Revue des Études Juives•1991

    King Madeleine. Le Cercle de généalogie juive. In: Revue des études juives, tome 150, n°1-2, janvier-juin 1991. pp. 161-162

  • Is general practitioner decision making associated with patient socio-economic status

    Open Access•Anthony Scott, Alan Shiell et al.•ARTICLE•Social Science & Medicine•1996•Cited by: 12•References: 41

  • Quality of life three months and one year after first treatment for early stage breast cancer

    Open Access•Madeleine King, M T King et al.•ARTICLE•Quality of Life Research•2000

  • Patterns over time in quality of life, coping and psychological adjustment in late stage melanoma patients

    Open Access•Judith Brown, J E Brown et al.•ARTICLE•Quality of Life Research•2000

  • Adaptation to changing health

    Open Access•Madeleine King•ARTICLE•Quality of Life Research•2002

  • A mother's choice

    Open Access•Alan Shiell, Sue Cameron et al.•ARTICLE•Health & Social Care in the…•2007

    An Early Discharge Programme (EDP) for medically uncomplicated obstetric patients operated from three hospitals in Sydney's western suburbs. A number of women who were eligible for this programme declined to take part. This study investigated the reasons why some women chose to remain longer in hospital rather than go home early with domiciliary midwifery support. The results showed a lack of awareness and information about the EDP, particularly …

  • A highly significant difference in baseline characteristics

    Open Access•Peter Fayers, Peter M Fayers et al.•ARTICLE•Quality of Life Research•2008

  • Measures of asthma control and quality of life

    Open Access•Madeleine King, Madeleine T King et al.•ARTICLE•Quality of Life Research•2009

  • How to guarantee finding a statistically significant difference

    Open Access•Peter Fayers, Peter M Fayers et al.•ARTICLE•Quality of Life Research•2009

  • Validation of modified forms of the PedsQL generic core scales and cancer module scales for adolescents and young adults (AYA) with cancer or a blood disorder

    Open Access•Jane Ewing, Jane E Ewing et al.•ARTICLE•Quality of Life Research•2009

    These modified forms provide reliable and valid measures of HRQOL in AYA with cancer or a blood disorder, suitable for clinical trials, research, and practice

  • Validation and calibration of the SF-36 health transition question against an external criterion of clinical change in health status

    Open Access•Stephanie A Knox, Stephanie Knox et al.•ARTICLE•Quality of Life Research•2009

  • Does mode of administration matter? Comparison of online and face-to-face administration of a time trade-off task

    Open Access•Richard Norman, Madeleine King et al.•ARTICLE•Quality of Life Research•2010

  • A comparison of the Fact-G and the Supportive Care Needs Survey (SCNS) in women with ovarian cancer

    Open Access•Ben Colagiuri, The Australian Ovarian Cancer Study—Quality of Life Study…•ARTICLE•Quality of Life Research•2011

  • Let’s engage the patient within us

    Open Access•Carolyn E Schwartz, Madeleine King et al.•ARTICLE•Quality of Life Research•2013

  • Psychometric evaluation of the EORTC computerized adaptive test (CAT) fatigue item pool

    Open Access•Morten Aagaard Petersen, Johannes M Giesinger et al.•ARTICLE•Quality of Life Research•2013

  • Clinical Use of Health-Related Quality of Life Outcomes From Cancer Clinical Trials

    Julie Rouette, Jane Blazeby et al.•ARTICLE•Journal of Epidemiology and…•2013

    Introduction There have been increasing efforts aimed at enhancing patient-centered care and incorporating patients' voice into clinical practice. As such, a growing body of literature has recognized the importance of Health-Related Quality of Life (HRQOL) outcomes from clinical trials. HRQOL outcomes are often collected in Phase III randomized controlled trials (RCTs), along with survival data, morbidity, and toxicity data. HRQOL outcomes are me…

  • Bias in Area Under the Curve for Longitudinal Clinical Trials With Missing Patient Reported Outcome Data

    Open Access•Melanie L Bell, Madeleine King et al.•ARTICLE•SAGE Open•2014

    A common approach to the analysis of longitudinal patient reported outcomes (PROs) is the use of summary measures such as area under the time curve (AUC). However, it is not clear how missing data affects the validity of AUC analysis. This study aimed to compare the use of AUC summary measures (in individuals) with AUC summary statistics (on groups, calculated from the estimated parameters of a mixed model) when data are complete, missing at rand…

  • Testing the measurement invariance of the EORTC QLQ-C30 across primary cancer sites using multi-group confirmatory factor analysis

    Open Access•Daniel Costa, D S J Costa et al.•ARTICLE•Quality of Life Research•2014

  • Using Rasch analysis to examine the distress thermometer’s cut-off scores among a mixed group of patients with cancer

    Open Access•Sylvie D Lambert, Julie Pallant et al.•ARTICLE•Quality of Life Research•2014

  • Assessing the invariance of a culturally competent multi-lingual unmet needs survey for immigrant and Australian-born cancer patients

    Open Access•Joshua McGrane, J A McGrane et al.•ARTICLE•Quality of Life Research•2014

  • Integrating health-related quality of life findings from randomized clinical trials into practice

    Open Access•Julie Rouette, Jane Blazeby et al.•ARTICLE•Quality of Life Research•2014

  • The physical functioning and mental health of informal carers

    Open Access•Patricia Kenny, Madeleine King et al.•ARTICLE•Health & Social Care in the…•2014•Cited by: 9•References: 3

    Informal carers represent a substantial proportion of the population in many countries and health is an important factor in their capacity to continue care-giving. This study investigated the impact of care-giving on the mental and physical health of informal carers, taking account of contextual factors, including family and work. We examined health changes from before care-giving commenced to 2 and 4 years after, using longitudinal data from the…

  • International Society for Quality of Life Research commentary on the draft European Medicines Agency reflection paper on the use of patient-reported outcome (PRO) measures in oncology studies

    Open Access•Derek Kyte, Bryce B Reeve et al.•ARTICLE•Quality of Life Research•2015

  • Using a discrete choice experiment to value the QLU-C10D

    Open Access•Richard Norman, Rowena Viney et al.•ARTICLE•Quality of Life Research•2015

  • Qlu-C10d

    Open Access•Madeleine King, M T King et al.•ARTICLE•Quality of Life Research•2016

Medicine (43 works) · Public health (26 works) · Psychology (24 works) · Nursing (22 works) · Health Systems, Economic Evaluations, Quality of Life (21 works) · Internal Medicine (20 works) · Quality of Life Research (20 works) · Quality of life (healthcare (19 works) · Cancer survivorship and care (14 works) · Gerontology (13 works)

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