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Claudio Russo

Biographic Data

ID6506210
NAMEClaudio Russo
GIVEN NAMESClaudio
FAMILY NAMERusso
SIGNATURERUSSO C
AFFILIATIONSUniversity of Salerno
ORCID0000-0003-4877-2424
VERIFIEDYes
TOTAL WORKS7
TOTAL CITATIONS12
WORKS AS AUTHOR7
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2019
LATEST PUBLICATION YEAR2025
H-INDEX1
  • Prolonged physical isolation, agonistic behaviour, and human resilience in pandemic times

    Open Access•Giuseppina Marsico, Claudio Russo•ARTICLE•Frontiers in Public Health•2025

    With the purpose of enhancing a comprehensive approach to healthcare, public health initiatives have moved from managing the pandemic response towards an increased understanding of the sequelae, including but not limited to mental health issues triggered by societal limitations and precautionary measures. The long-term effects of the COVID-19 pandemic lie in the health system’s capacity to promote a renewed sense of healthy communities, strengthe…

  • Caregivers’ Burden in Parkinson’s Disease

    Open Access•Luna Carpinelli, Giulia Savarese et al.•ARTICLE•Human Arenas•2025

    Parkinson’s disease (PD) is a chronic progressive neurological disease clinically characterized by motor and non-motor symptoms, with an increasing impact on the quality of life not only for the patient but also for the caregivers. Twenty-six primary caregivers (female = 19; mean age = 57.04, SD = 10.64) of PD patients were consecutively recruited. Several psychological aspects were verified through clinical screening tests: EQ-5D and PQoL CARER …

  • Multiple System Atrophy (MSA) and the Family Caregivers’ Burden

    Open Access•Giulia Savarese, Luna Carpinelli et al.•ARTICLE•Human Arenas•2024

    Multiple systemic atrophy (MSA) is a progressive neurodegenerative disease, also characterized by autonomic failure in varying degrees of severity. Caregivers are central to the care and support of people with MSA. This paper aims to investigate and discuss: (a) the most common emotions and reactions among caregivers of MSA patients and how these affect their psychological well-being, (b) the change in caregivers’ quality of life during the progr…

  • An Inclusive Workplace Approach to Disability through Assistive Technologies

    Open Access•Tiziana Marinaci, Claudio Russo et al.•ARTICLE•Societies•2023

    To explain the low employment rates of people with disabilities (PwDs), emerging debates have revealed an unexploited potential impact of assistive technology (AT) on human talent and the inclusion process. This article provides a systematic review to critically evaluate the current trends in the literature on AT. A systematic review was performed according to the inclusion criteria of the PRISMA-S guidelines, followed by a thematic analysis iden…

  • Mandatory provisioning of digital public services as a feasible service delivery strategy

    Open Access•Luca Tangi, Michele Benedetti et al.•ARTICLE•Government Information Quarterly•2020•Cited by: 12•References: 16

  • The Group Benefits of Mindfulness Meditation in Education and Mental Health Care

    Open Access•Claudio Russo•ARTICLE•Human Arenas•2019

  • Coping, Mood, Quality of Life, and Outcomes in Recipients of Left Ventricular Assist Devices

    Maddalena Modica, Anna Minotti et al.•ARTICLE•Psychosomatic Medicine•2019

    OBJECTIVE: Left ventricular assist devices (LVADs) are increasingly used for temporary circulatory support until transplant or as destination therapy for patients with end-stage heart failure. Understanding patients' attitudes and resources is crucial to support them. METHODS: Sixty-one LVAD recipients (55 [10] years, 10% women, 15% destination therapy) participating in cardiac rehabilitation (CR) postimplant underwent assessment of coping styles…

  • Mandatory provisioning of digital public services as a feasible service delivery strategy

    Open Access•Luca Tangi, Michele Benedetti et al.•ARTICLE•Government Information Quarterly•2020•Cited by: 12•References: 16

  • The Group Benefits of Mindfulness Meditation in Education and Mental Health Care

    Open Access•Claudio Russo•ARTICLE•Human Arenas•2019

  • Coping, Mood, Quality of Life, and Outcomes in Recipients of Left Ventricular Assist Devices

    Maddalena Modica, Anna Minotti et al.•ARTICLE•Psychosomatic Medicine•2019

    OBJECTIVE: Left ventricular assist devices (LVADs) are increasingly used for temporary circulatory support until transplant or as destination therapy for patients with end-stage heart failure. Understanding patients' attitudes and resources is crucial to support them. METHODS: Sixty-one LVAD recipients (55 [10] years, 10% women, 15% destination therapy) participating in cardiac rehabilitation (CR) postimplant underwent assessment of coping styles…

  • Mandatory provisioning of digital public services as a feasible service delivery strategy

    Open Access•Luca Tangi, Michele Benedetti et al.•ARTICLE•Government Information Quarterly•2020•Cited by: 12•References: 16

  • An Inclusive Workplace Approach to Disability through Assistive Technologies

    Open Access•Tiziana Marinaci, Claudio Russo et al.•ARTICLE•Societies•2023

    To explain the low employment rates of people with disabilities (PwDs), emerging debates have revealed an unexploited potential impact of assistive technology (AT) on human talent and the inclusion process. This article provides a systematic review to critically evaluate the current trends in the literature on AT. A systematic review was performed according to the inclusion criteria of the PRISMA-S guidelines, followed by a thematic analysis iden…

  • Multiple System Atrophy (MSA) and the Family Caregivers’ Burden

    Open Access•Giulia Savarese, Luna Carpinelli et al.•ARTICLE•Human Arenas•2024

    Multiple systemic atrophy (MSA) is a progressive neurodegenerative disease, also characterized by autonomic failure in varying degrees of severity. Caregivers are central to the care and support of people with MSA. This paper aims to investigate and discuss: (a) the most common emotions and reactions among caregivers of MSA patients and how these affect their psychological well-being, (b) the change in caregivers’ quality of life during the progr…

  • Prolonged physical isolation, agonistic behaviour, and human resilience in pandemic times

    Open Access•Giuseppina Marsico, Claudio Russo•ARTICLE•Frontiers in Public Health•2025

    With the purpose of enhancing a comprehensive approach to healthcare, public health initiatives have moved from managing the pandemic response towards an increased understanding of the sequelae, including but not limited to mental health issues triggered by societal limitations and precautionary measures. The long-term effects of the COVID-19 pandemic lie in the health system’s capacity to promote a renewed sense of healthy communities, strengthe…

  • Caregivers’ Burden in Parkinson’s Disease

    Open Access•Luna Carpinelli, Giulia Savarese et al.•ARTICLE•Human Arenas•2025

    Parkinson’s disease (PD) is a chronic progressive neurological disease clinically characterized by motor and non-motor symptoms, with an increasing impact on the quality of life not only for the patient but also for the caregivers. Twenty-six primary caregivers (female = 19; mean age = 57.04, SD = 10.64) of PD patients were consecutively recruited. Several psychological aspects were verified through clinical screening tests: EQ-5D and PQoL CARER …

Medicine (4 works) · Psychiatry (4 works) · Psychology (4 works) · Clinical Psychology (3 works) · Anxiety (2 works) · Disease (2 works) · Gerontology (2 works) · Hospital Anxiety and Depression Scale (2 works) · Internal Medicine (2 works) · Physical therapy (2 works)

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