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Patient perspectives on digital healthcare technology in care and clinical trials for motor neuron disease: an international survey.
Helleman, Jochem; Johnson, Barbara; Holdom, Cory; Hobson, Esther; Murray, Deirdre; Steyn, Frederik J; Ngo, Shyuan T; Henders, Anjali; Lokeshappa, Madhura B; Visser-Meily, Johanna M A; van den Berg, Leonard H; Hardiman, Orla; Beelen, Anita; McDermott, Chris; van Eijk, Ruben P A.
Afiliação
  • Helleman J; Department of Rehabilitation, Physical Therapy Science and Sports, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Johnson B; Center of Excellence for Rehabilitation Medicine, UMC Utrecht Brain Center, University Medical Center Utrecht, and De Hoogstraat Rehabilitation, Utrecht, the Netherlands.
  • Holdom C; Department of Neuroscience, Sheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield, UK.
  • Hobson E; Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, Australia.
  • Murray D; UQ Centre for Clinical Research, The University of Queensland, Brisbane, Australia.
  • Steyn FJ; Department of Neuroscience, Sheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield, UK.
  • Ngo ST; Academic Unit of Neurology, Trinity College Dublin, Dublin, Ireland.
  • Henders A; Physiotherapy Department, Beaumont Hospital, Dublin, Ireland.
  • Lokeshappa MB; School of Biomedical Sciences, Faculty of Medicine, University of Queensland, Brisbane, Australia.
  • Visser-Meily JMA; The Royal Brisbane and Women's Hospital, Herston, Australia.
  • van den Berg LH; Wesley Medical Research, The Wesley Hospital, Auchenflower, Australia.
  • Hardiman O; Centre for Clinical Research, The University of Queensland, Brisbane, Australia.
  • Beelen A; Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, Australia.
  • McDermott C; The Royal Brisbane and Women's Hospital, Herston, Australia.
  • van Eijk RPA; Centre for Clinical Research, The University of Queensland, Brisbane, Australia.
J Neurol ; 269(11): 6003-6013, 2022 Nov.
Article em En | MEDLINE | ID: mdl-35849154
ABSTRACT

INTRODUCTION:

To capture the patient's attitude toward remote monitoring of motor neuron disease (MND) in care and clinical trials, and their concerns and preferences regarding the use of digital technology.

METHODS:

We performed an international multi-centre survey study in three MND clinics in The Netherlands, the United Kingdom, and Australia. The survey was co-developed by investigators and patients with MND, and sent to patients by e-mail or postal-mail. The main topics included patients' attitude towards remote care, participating in decentralized clinical trials, and preferences for and concerns with digital technology use.

RESULTS:

In total, 332 patients with MND participated. A majority of patients indicated they would be happy to self-monitor their health from home (69%), be remotely monitored by a multidisciplinary care team (75%), and would be willing to participate in clinical trials from home (65%). Patients considered respiratory function and muscle strength most valuable for home-monitoring. The majority of patients considered the use of at least three devices/apps (75%) once a week (61%) to be acceptable for home-monitoring. Fifteen percent of patients indicated they would not wish to perform home-measurements; reporting concerns about the burden and distress of home-monitoring, privacy and data security.

CONCLUSION:

Most patients with MND exhibited a positive attitude toward the use of digital technology in both care and clinical trial settings. A subgroup of patients reported concerns with home-monitoring, which should be addressed in order to improve widespread adoption of remote digital technology in clinical MND care.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença dos Neurônios Motores / Esclerose Lateral Amiotrófica Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: J Neurol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença dos Neurônios Motores / Esclerose Lateral Amiotrófica Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: J Neurol Ano de publicação: 2022 Tipo de documento: Article