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Albine Moser

Biographic Data

ID4218996
NAMEAlbine Moser
GIVEN NAMESAlbine
FAMILY NAMEMoser
SIGNATUREMOSER A
AFFILIATIONSZuyd University of Applied Sciences
ORCID0000-0003-4073-2890
VERIFIEDYes
TOTAL WORKS12
TOTAL CITATIONS2
AUTHOR COUNT12
EDITOR COUNT0
FIRST PUBLICATION YEAR2008
LATEST PUBLICATION YEAR2025
H-INDEX1
  • Sustainability of interprofessional team meetings for vulnerable elderly people living at home

    Open Access•Jelena Slowig, Albine Moser et al.•ARTICLE•International Journal of…•2025

    Background: Older adults experiences multiple health difficulties and often require complex care. Several healthcare professionals in primary care such as general practitioners, nurses and paramedics are involved in their care. To coordinate complex care, case meetings between these healthcare professionals are held, so called interprofessional team meetings (ITM). However, it is a challenge to sustainably hold these meetings due to several facto…

  • Implementation of a patient‐reported experience measure in a Dutch disability care organization

    Open Access•Marjolein van Rooijen, Anneke van Dijk‐de Vries et al.•ARTICLE•Health Expectations•2023

    INTRODUCTION: In 24/7 disability care facilities, patient-reported experience measures (PREMs) are important to help healthcare professionals understand what matters to care users and to improve the quality of care. However, the successful implementation of a PREM is complex. In a Dutch disability care organization, stakeholders cocreated tailored implementation strategies aimed at improving the use and integration of a qualitative PREM. This stu…

  • Patient and public involvement cultures and the perceived impact in the vulnerable context of palliative care

    Open Access•Inge Melchior, Anouk van der Heijden et al.•ARTICLE•Health Expectations•2021

    BACKGROUND: Cultural values are crucial to the practice and impact of patient and public involvement (PPI) in research. OBJECTIVE: To understand different PPI cultures among research teams and the impacts of PPI associated with each culture type. DESIGN: A participatory action research design. SETTING AND PARTICIPANTS: The setting was 10 palliative care research projects. Seventeen patients and members of the public and 31 researchers participate…

  • Improving the experience of older people with colorectal and breast cancer in patient‐centred cancer care pathways using experience‐based co‐design

    Open Access•Albine Moser, Inge Melchior et al.•ARTICLE•Health Expectations•2021

    BACKGROUND: Patient and public involvement (PPI) in quality improvement of oncological care pathways for older patients are rare. OBJECTIVES: Improve the care pathway experience of older cancer patients and explore lessons learned regarding how to engage this vulnerable group. DESIGN: Experience-Based Co-Design. SETTING AND PARTICIPANTS: Older cancer patients, their caregivers and healthcare professionals within colorectal and breast cancer care …

  • Stakeholder engagement from problem analysis to implementation strategies for a patient‐reported experience measure in disability care

    Open Access•Marjolein van Rooijen, Stephanie Lenzen et al.•ARTICLE•Health Expectations•2021

    BACKGROUND: In implementation science, vast gaps exist between theoretical and practical knowledge. These gaps prevail in the process of getting from problem analysis to selecting implementation strategies while engaging stakeholders including care users. OBJECTIVE: To describe a process of how to get from problem analysis to strategy selection, how to engage stakeholders, and to provide insights into stakeholders' experiences. DESIGN: A qualitat…

  • Clients and professionals elicit long‐term care preferences by using ‘What matters to me’

    Open Access•Catharina Margaretha van Leersum, Albine Moser et al.•ARTICLE•Health & Social Care in the…•2021•Cited by: 1•References: 2

    What matters to me' seems useful to assist clients and professionals with preference elicitation in long-term care. Evaluation of the impact on consultations between clients and professionals by using 'What matters to me' is needed

  • Preparing researchers for patient and public involvement in scientific research

    Open Access•Maya De Wit, Anna Beurskens et al.•ARTICLE•Health Expectations•2018

    BACKGROUND: Acquiring the theoretical and practical knowhow of conducting patient and public involvement (PPI) in research is not part of the traditional curriculum of researchers. Zuyd University of Applied Sciences and Huis voor de Zorg, a regional umbrella patient organization, therefore started a 1.5-year coaching programme. OBJECTIVE: To establish a community of practice by developing a PPI coaching programme for senior and junior health ser…

  • Integrated care

    Open Access•Dirk Ruwaard, Katja van Vliet et al.•ARTICLE•International Journal of…•2018

    The International Journal of Integrated Care (IJIC) is an online, open-access, peer-reviewed scientific journal that publishes original articles in the field of integrated care on a continuous basis.IJIC has an Impact Factor of 5.120 (2020 JCR, received in June 2021)

  • Series

    Open Access•Irene Korstjens, Albine Moser•ARTICLE•European Journal of General…•2017

    In the course of our supervisory work over the years, we have noticed that qualitative research tends to evoke a lot of questions and worries, so-called frequently asked questions (FAQs). This series of four articles intends to provide novice researchers with practical guidance for conducting high-quality qualitative research in primary care. By 'novice' we mean Master's students and junior researchers, as well as experienced quantitative researc…

  • The perceived impact of public involvement in palliative care in a provincial palliative care network in the N etherlands

    Open Access•Frederike Haarsma, Frederike A Haarsma et al.•ARTICLE•Health Expectations•2015

    BACKGROUND AND OBJECTIVE: Public involvement in palliative care is challenging and difficult, because people in need of palliative care are often not capable of speaking up for themselves. Patient representatives advocate for their common interests. The aim of our study was to examine in depth the current practice of public involvement in palliative care. SETTING AND SAMPLE: The study was conducted in the province of Limburg in the Netherlands, w…

  • Using the Obser-View in Qualitative Research

    Open Access•Linda Kragelund, Albine Moser et al.•ARTICLE•International Journal of…•2015•Cited by: 1•References: 15

    The obser-view is a method to generate data and create a learning space for both researcher and participants in qualitative research. It includes reflection between the two after the researcher has observed the participant. This article aims to reveal the benefits and challenges encountered when using the obser-view in two different research projects. In a Dutch project whose aim was to empower residents with dementia, in nursing homes the obser-…

  • Self-management of type 2 diabetes mellitus

    Open Access•Albine Moser, Harry van der Bruggen et al.•ARTICLE•BMC Public Health•2008

    Self-management consists of a complex and dynamic set of processes and it is deeply embedded in one's unique life situation. Support from diabetes specialist nurses and family caregivers is a necessity of self-managing diabetes

  • Clients and professionals elicit long‐term care preferences by using ‘What matters to me’

    Open Access•Catharina Margaretha van Leersum, Albine Moser et al.•ARTICLE•Health & Social Care in the…•2021•Cited by: 1•References: 2

    What matters to me' seems useful to assist clients and professionals with preference elicitation in long-term care. Evaluation of the impact on consultations between clients and professionals by using 'What matters to me' is needed

  • Using the Obser-View in Qualitative Research

    Open Access•Linda Kragelund, Albine Moser et al.•ARTICLE•International Journal of…•2015•Cited by: 1•References: 15

    The obser-view is a method to generate data and create a learning space for both researcher and participants in qualitative research. It includes reflection between the two after the researcher has observed the participant. This article aims to reveal the benefits and challenges encountered when using the obser-view in two different research projects. In a Dutch project whose aim was to empower residents with dementia, in nursing homes the obser-…

  • Self-management of type 2 diabetes mellitus

    Open Access•Albine Moser, Harry van der Bruggen et al.•ARTICLE•BMC Public Health•2008

    Self-management consists of a complex and dynamic set of processes and it is deeply embedded in one's unique life situation. Support from diabetes specialist nurses and family caregivers is a necessity of self-managing diabetes

  • The perceived impact of public involvement in palliative care in a provincial palliative care network in the N etherlands

    Open Access•Frederike Haarsma, Frederike A Haarsma et al.•ARTICLE•Health Expectations•2015

    BACKGROUND AND OBJECTIVE: Public involvement in palliative care is challenging and difficult, because people in need of palliative care are often not capable of speaking up for themselves. Patient representatives advocate for their common interests. The aim of our study was to examine in depth the current practice of public involvement in palliative care. SETTING AND SAMPLE: The study was conducted in the province of Limburg in the Netherlands, w…

  • Using the Obser-View in Qualitative Research

    Open Access•Linda Kragelund, Albine Moser et al.•ARTICLE•International Journal of…•2015•Cited by: 1•References: 15

    The obser-view is a method to generate data and create a learning space for both researcher and participants in qualitative research. It includes reflection between the two after the researcher has observed the participant. This article aims to reveal the benefits and challenges encountered when using the obser-view in two different research projects. In a Dutch project whose aim was to empower residents with dementia, in nursing homes the obser-…

  • Series

    Open Access•Irene Korstjens, Albine Moser•ARTICLE•European Journal of General…•2017

    In the course of our supervisory work over the years, we have noticed that qualitative research tends to evoke a lot of questions and worries, so-called frequently asked questions (FAQs). This series of four articles intends to provide novice researchers with practical guidance for conducting high-quality qualitative research in primary care. By 'novice' we mean Master's students and junior researchers, as well as experienced quantitative researc…

  • Preparing researchers for patient and public involvement in scientific research

    Open Access•Maya De Wit, Anna Beurskens et al.•ARTICLE•Health Expectations•2018

    BACKGROUND: Acquiring the theoretical and practical knowhow of conducting patient and public involvement (PPI) in research is not part of the traditional curriculum of researchers. Zuyd University of Applied Sciences and Huis voor de Zorg, a regional umbrella patient organization, therefore started a 1.5-year coaching programme. OBJECTIVE: To establish a community of practice by developing a PPI coaching programme for senior and junior health ser…

  • Integrated care

    Open Access•Dirk Ruwaard, Katja van Vliet et al.•ARTICLE•International Journal of…•2018

    The International Journal of Integrated Care (IJIC) is an online, open-access, peer-reviewed scientific journal that publishes original articles in the field of integrated care on a continuous basis.IJIC has an Impact Factor of 5.120 (2020 JCR, received in June 2021)

  • Patient and public involvement cultures and the perceived impact in the vulnerable context of palliative care

    Open Access•Inge Melchior, Anouk van der Heijden et al.•ARTICLE•Health Expectations•2021

    BACKGROUND: Cultural values are crucial to the practice and impact of patient and public involvement (PPI) in research. OBJECTIVE: To understand different PPI cultures among research teams and the impacts of PPI associated with each culture type. DESIGN: A participatory action research design. SETTING AND PARTICIPANTS: The setting was 10 palliative care research projects. Seventeen patients and members of the public and 31 researchers participate…

  • Improving the experience of older people with colorectal and breast cancer in patient‐centred cancer care pathways using experience‐based co‐design

    Open Access•Albine Moser, Inge Melchior et al.•ARTICLE•Health Expectations•2021

    BACKGROUND: Patient and public involvement (PPI) in quality improvement of oncological care pathways for older patients are rare. OBJECTIVES: Improve the care pathway experience of older cancer patients and explore lessons learned regarding how to engage this vulnerable group. DESIGN: Experience-Based Co-Design. SETTING AND PARTICIPANTS: Older cancer patients, their caregivers and healthcare professionals within colorectal and breast cancer care …

  • Stakeholder engagement from problem analysis to implementation strategies for a patient‐reported experience measure in disability care

    Open Access•Marjolein van Rooijen, Stephanie Lenzen et al.•ARTICLE•Health Expectations•2021

    BACKGROUND: In implementation science, vast gaps exist between theoretical and practical knowledge. These gaps prevail in the process of getting from problem analysis to selecting implementation strategies while engaging stakeholders including care users. OBJECTIVE: To describe a process of how to get from problem analysis to strategy selection, how to engage stakeholders, and to provide insights into stakeholders' experiences. DESIGN: A qualitat…

  • Clients and professionals elicit long‐term care preferences by using ‘What matters to me’

    Open Access•Catharina Margaretha van Leersum, Albine Moser et al.•ARTICLE•Health & Social Care in the…•2021•Cited by: 1•References: 2

    What matters to me' seems useful to assist clients and professionals with preference elicitation in long-term care. Evaluation of the impact on consultations between clients and professionals by using 'What matters to me' is needed

  • Implementation of a patient‐reported experience measure in a Dutch disability care organization

    Open Access•Marjolein van Rooijen, Anneke van Dijk‐de Vries et al.•ARTICLE•Health Expectations•2023

    INTRODUCTION: In 24/7 disability care facilities, patient-reported experience measures (PREMs) are important to help healthcare professionals understand what matters to care users and to improve the quality of care. However, the successful implementation of a PREM is complex. In a Dutch disability care organization, stakeholders cocreated tailored implementation strategies aimed at improving the use and integration of a qualitative PREM. This stu…

  • Sustainability of interprofessional team meetings for vulnerable elderly people living at home

    Open Access•Jelena Slowig, Albine Moser et al.•ARTICLE•International Journal of…•2025

    Background: Older adults experiences multiple health difficulties and often require complex care. Several healthcare professionals in primary care such as general practitioners, nurses and paramedics are involved in their care. To coordinate complex care, case meetings between these healthcare professionals are held, so called interprofessional team meetings (ITM). However, it is a challenge to sustainably hold these meetings due to several facto…

Medicine (10 works) · Nursing (9 works) · Psychology (8 works) · Qualitative research (8 works) · Mental Health and Patient Involvement (7 works) · Health Policy Implementation Science (6 works) · Political science (6 works) · Sociology (6 works) · Computer Science (5 works) · Patient-Provider Communication in Healthcare (5 works)

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