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Madeleine T King

Biographic Data

ID5544931
NAMEMadeleine T King
GIVEN NAMESMadeleine T
FAMILY NAMEKing
SIGNATUREKING M T
AFFILIATIONSQOL Office, Level 6 North, Lifehouse (C39Z), University of Sydney, Sydney, NSW, Australia
VERIFIEDNo
TOTAL WORKS19
TOTAL CITATIONS10
AUTHOR COUNT19
EDITOR COUNT0
FIRST PUBLICATION YEAR2009
LATEST PUBLICATION YEAR2024
H-INDEX1
  • 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

  • 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

  • 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

  • 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…

  • 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

  • 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

  • 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…

  • 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

  • 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…

  • 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

  • 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

  • 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

  • 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, …

  • 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

  • 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

  • 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…

  • 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

  • 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

  • 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, …

  • 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

  • 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

  • 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…

  • 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

  • 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

  • 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

Medicine (18 works) · Internal Medicine (11 works) · Psychology (11 works) · Clinical Psychology (10 works) · Public health (9 works) · Clinical Psychology (8 works) · Health Systems, Economic Evaluations, Quality of Life (8 works) · Psychiatry (8 works) · Cancer survivorship and care (7 works) · Quality of life (healthcare (7 works)

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