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Wolter Paans

Biographic Data

ID6577175
NAMEWolter Paans
GIVEN NAMESWolter
FAMILY NAMEPaans
SIGNATUREPAANS W
AFFILIATIONSResearch Group Nursing Diagnostics Hanze University of Applied Sciences Groningen The Netherlands
ORCID0000-0001-9909-4833
VERIFIEDYes
TOTAL WORKS6
TOTAL CITATIONS0
WORKS AS AUTHOR6
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2019
LATEST PUBLICATION YEAR2023
H-INDEX0
  • Identifying and Supporting Students with a Chronically Ill Family Member

    Open Access•Hinke M van der Werf, Wolter Paans et al.•ARTICLE•International Journal of…•2023

    Young adult caregivers experience reduced wellbeing when the combination of family care and an educational program becomes too demanding. We aim to clarify the role views, competences, and needs of lecturers regarding the identification and support of these students to prevent negative mental health consequences. A mixed-methods explanatory sequential design was used. We collected quantitative data using a survey of lecturers teaching in bachelor…

  • Patient participation in electronic nursing documentation

    Open Access•Kim de Groot, Judith Douma et al.•ARTICLE•Health Expectations•2022

    BACKGROUND: Patients are increasingly expected to take an active role in their own care. Participation in nursing documentation can support patients to take this active role since it provides opportunities to express care needs and preferences. Yet, patient participation in electronic nursing documentation is not self-evident. OBJECTIVE: To explore how home-care patients perceive their participation in electronic nursing documentation. METHODS: S…

  • Expectations and Prospects of Young Adult Caregivers Regarding the Support of Professionals

    Open Access•Hinke M van der Werf, Wolter Paans et al.•ARTICLE•International Journal of…•2020

    There is a lack of service provision for young adult caregivers (18-25 years of age). This study aims to describe the expectations and prospects of young adult caregivers regarding support from health and education professionals. A qualitative focus group design was used. Twenty-five young Dutch adults (aged 18-25 years) who were growing up with a chronically ill family member participated in one of seven focus groups. Qualitative inductive analy…

  • Patients' and family members' perspectives on the benefits and working mechanisms of family nursing conversations in Dutch home healthcare

    Open Access•Susanne Broekema, Wolter Paans et al.•ARTICLE•Health & Social Care in the…•2020

    The aim of this study is to propose a model of the benefits and working mechanisms of family nursing conversations in home healthcare from the perspective of participating patients and their family members. Family nursing conversations in this study are intended to optimise family functioning, improve collaboration between family and professional caregivers and ultimately prevent or reduce overburden of family caregivers. In a qualitative grounde…

  • Students growing up with a chronically ill family member; a survey on experienced consequences, background characteristics, and risk factors

    Open Access•Hinke M van der Werf, Marie Louise Luttik et al.•ARTICLE•BMC Public Health•2019

    Since a substantial number of students growing up with a chronically ill family member indicate serious physical, mental, and social consequences as a result of this care situation, awareness for this specific age-group is needed. Students with a mentally ill family member and students undertaking vocational education appear to be especially at risk. Further research is required in order to gain insight that is more in-depth into the exact type o…

  • Experiences of Dutch students growing up with a family member with a chronic illness

    Open Access•Hinke M van der Werf, Wolter Paans et al.•ARTICLE•Health & Social Care in the…•2019•References: 1

    Students growing up with a family member with a chronic illness often delay or drop out of school when the combination of family care and their educational programme is too demanding. This study aims to describe the themes experienced by students growing up in this situation. A qualitative focus group design was used. The recruitment for this study was done through an online survey where students could indicate whether they also wanted to partici…

No prominent works on this page.

  • Students growing up with a chronically ill family member; a survey on experienced consequences, background characteristics, and risk factors

    Open Access•Hinke M van der Werf, Marie Louise Luttik et al.•ARTICLE•BMC Public Health•2019

    Since a substantial number of students growing up with a chronically ill family member indicate serious physical, mental, and social consequences as a result of this care situation, awareness for this specific age-group is needed. Students with a mentally ill family member and students undertaking vocational education appear to be especially at risk. Further research is required in order to gain insight that is more in-depth into the exact type o…

  • Experiences of Dutch students growing up with a family member with a chronic illness

    Open Access•Hinke M van der Werf, Wolter Paans et al.•ARTICLE•Health & Social Care in the…•2019•References: 1

    Students growing up with a family member with a chronic illness often delay or drop out of school when the combination of family care and their educational programme is too demanding. This study aims to describe the themes experienced by students growing up in this situation. A qualitative focus group design was used. The recruitment for this study was done through an online survey where students could indicate whether they also wanted to partici…

  • Expectations and Prospects of Young Adult Caregivers Regarding the Support of Professionals

    Open Access•Hinke M van der Werf, Wolter Paans et al.•ARTICLE•International Journal of…•2020

    There is a lack of service provision for young adult caregivers (18-25 years of age). This study aims to describe the expectations and prospects of young adult caregivers regarding support from health and education professionals. A qualitative focus group design was used. Twenty-five young Dutch adults (aged 18-25 years) who were growing up with a chronically ill family member participated in one of seven focus groups. Qualitative inductive analy…

  • Patients' and family members' perspectives on the benefits and working mechanisms of family nursing conversations in Dutch home healthcare

    Open Access•Susanne Broekema, Wolter Paans et al.•ARTICLE•Health & Social Care in the…•2020

    The aim of this study is to propose a model of the benefits and working mechanisms of family nursing conversations in home healthcare from the perspective of participating patients and their family members. Family nursing conversations in this study are intended to optimise family functioning, improve collaboration between family and professional caregivers and ultimately prevent or reduce overburden of family caregivers. In a qualitative grounde…

  • Patient participation in electronic nursing documentation

    Open Access•Kim de Groot, Judith Douma et al.•ARTICLE•Health Expectations•2022

    BACKGROUND: Patients are increasingly expected to take an active role in their own care. Participation in nursing documentation can support patients to take this active role since it provides opportunities to express care needs and preferences. Yet, patient participation in electronic nursing documentation is not self-evident. OBJECTIVE: To explore how home-care patients perceive their participation in electronic nursing documentation. METHODS: S…

  • Identifying and Supporting Students with a Chronically Ill Family Member

    Open Access•Hinke M van der Werf, Wolter Paans et al.•ARTICLE•International Journal of…•2023

    Young adult caregivers experience reduced wellbeing when the combination of family care and an educational program becomes too demanding. We aim to clarify the role views, competences, and needs of lecturers regarding the identification and support of these students to prevent negative mental health consequences. A mixed-methods explanatory sequential design was used. We collected quantitative data using a survey of lecturers teaching in bachelor…

Medicine (6 works) · Psychology (6 works) · Family Support in Illness (5 works) · Qualitative research (5 works) · Nursing (4 works) · Family medicine (3 works) · Family member (3 works) · Sociology (3 works) · Bachelor (2 works) · Childhood Cancer Survivors' Quality of Life (2 works)

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