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Parkinson's disease patients' needs during the COVID-19 pandemic in a red zone: A framework analysis of open-ended survey questions.
Cavallieri, Francesco; Sireci, Francesca; Fioravanti, Valentina; Toschi, Giulia; Rispoli, Vittorio; Antonelli, Francesca; Costantini, Massimo; Ghirotto, Luca; Valzania, Franco.
  • Cavallieri F; Neurology Unit, Neuromotor & Rehabilitation Department, Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.
  • Sireci F; Clinical and Experimental Medicine PhD Program, University of Modena and Reggio Emilia, Modena, Italy.
  • Fioravanti V; Neurology Unit, Neuromotor & Rehabilitation Department, Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.
  • Toschi G; Neurology Unit, Neuromotor & Rehabilitation Department, Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.
  • Rispoli V; Neurology Unit, Neuromotor & Rehabilitation Department, Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.
  • Antonelli F; Neurology, Neuroscience, Head and Neck Department, University of Modena and Reggio Emilia, Modena, Italy.
  • Costantini M; Neurology, Neuroscience, Head and Neck Department, University of Modena and Reggio Emilia, Modena, Italy.
  • Ghirotto L; Scientific Directorate, Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.
  • Valzania F; Qualitative Research Unit, Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Eur J Neurol ; 28(10): 3254-3262, 2021 10.
Article in English | MEDLINE | ID: covidwho-1604147
ABSTRACT
BACKGROUND AND

PURPOSE:

During the first phase of the COVID-19 pandemic, a lockdown was imposed in Italy. The aim of this study was to investigate the perceptions, feelings and unmet needs of Parkinson's disease (PD) patients who experienced the 2-month lockdown in a "red zone" in the northern part of Italy during the COVID-19 outbreak.

METHODS:

The study had a descriptive design that used a cross-sectional online survey which included open-ended questions to elicit responses on the participant's feelings concerning their risk of contracting coronavirus, how their physical activity had changed, and their personal needs, dictated by their condition, which were not met in this pandemic period as compared to previous periods. Demographic data were analysed using descriptive frequencies, while the open-ended questions were analysed using thematic framework analysis.

RESULTS:

The study included 103 participants (63 men/40 women [61.17 vs. 38.83%]). Framework analysis led to the identification of four main themes (i) fearing the risk of contracting coronavirus; (ii) reduction of physical activity; (iii) perception of the risk of not being able to access outpatient clinics or support services; and (iv) negative experiences of the important reduction in socialization. The perceptions of unmet needs appeared to be greater than the actual experience, particularly for the reduction in physical activity and the interruption of contacts with the neurologist and other specialists.

CONCLUSIONS:

This study highlights how perceptions and actual experience shape the meaning of living with PD during the pandemic. Worth noting is the divergence between perceptions and real impact in some aspects of the COVID-19 outbreak.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Parkinson Disease / COVID-19 Type of study: Observational study / Prognostic study / Qualitative research / Randomized controlled trials Limits: Female / Humans / Male Language: English Journal: Eur J Neurol Journal subject: Neurology Year: 2021 Document Type: Article Affiliation country: Ene.14745

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Parkinson Disease / COVID-19 Type of study: Observational study / Prognostic study / Qualitative research / Randomized controlled trials Limits: Female / Humans / Male Language: English Journal: Eur J Neurol Journal subject: Neurology Year: 2021 Document Type: Article Affiliation country: Ene.14745