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Assessment of the Effectiveness, Socio-Economic Impact and Implementation of a Digital Solution for Patients with Advanced Chronic Diseases: The ADLIFE Study Protocol.
García-Lorenzo, Borja; Gorostiza, Ania; González, Nerea; Larrañaga, Igor; Mateo-Abad, Maider; Ortega-Gil, Ana; Bloemeke, Janika; Groene, Oliver; Vergara, Itziar; Mar, Javier; Lim Choi Keung, Sarah N; Arvanitis, Theodoros N; Kaye, Rachelle; Dahary Halevy, Elinor; Nahir, Baraka; Arndt, Fritz; Dichmann Sorknæs, Anne; Juul, Natassia Kamilla; Lilja, Mikael; Sherman, Marie Holm; Laleci Erturkmen, Gokce Banu; Yuksel, Mustafa; Robbins, Tim; Kyrou, Ioannis; Randeva, Harpal; Maguire, Roma; McCann, Lisa; Miller, Morven; Moore, Margaret; Connaghan, John; Fullaondo, Ane; Verdoy, Dolores; de Manuel Keenoy, Esteban.
Afiliação
  • García-Lorenzo B; Kronikgune Institute for Health Services Research, Ronda de Azkue 1, Torre del Bilbao Exhibition Centre, 48902 Barakaldo, Basque Country, Spain.
  • Gorostiza A; Kronikgune Institute for Health Services Research, Ronda de Azkue 1, Torre del Bilbao Exhibition Centre, 48902 Barakaldo, Basque Country, Spain.
  • González N; Kronikgune Institute for Health Services Research, Ronda de Azkue 1, Torre del Bilbao Exhibition Centre, 48902 Barakaldo, Basque Country, Spain.
  • Larrañaga I; Osakidetza Basque Health Service, Barrualde-Galdakao, Integrated Health Organisation, 48960 Galdakao, Spain.
  • Mateo-Abad M; Kronikgune Institute for Health Services Research, Ronda de Azkue 1, Torre del Bilbao Exhibition Centre, 48902 Barakaldo, Basque Country, Spain.
  • Ortega-Gil A; Kronikgune Institute for Health Services Research, Ronda de Azkue 1, Torre del Bilbao Exhibition Centre, 48902 Barakaldo, Basque Country, Spain.
  • Bloemeke J; Biodonostia Health Research Institute, Paseo Dr. Begiristain s/n, 20014 Donostia, Basque Country, Spain.
  • Groene O; Kronikgune Institute for Health Services Research, Ronda de Azkue 1, Torre del Bilbao Exhibition Centre, 48902 Barakaldo, Basque Country, Spain.
  • Vergara I; OptiMedis, Burchardstrasse 17, 20095 Hamburg, Germany.
  • Mar J; OptiMedis, Burchardstrasse 17, 20095 Hamburg, Germany.
  • Lim Choi Keung SN; Biodonostia Health Research Institute, Paseo Dr. Begiristain s/n, 20014 Donostia, Basque Country, Spain.
  • Arvanitis TN; Kronikgune Institute for Health Services Research, Ronda de Azkue 1, Torre del Bilbao Exhibition Centre, 48902 Barakaldo, Basque Country, Spain.
  • Kaye R; Unidad de Investigación AP-OSIs, Hospital Alto Deba, 20500 Arrasate-Mondragón, Gipuzkoa, Spain.
  • Dahary Halevy E; Instituto de Investigación Sanitaria Biodonostia, 20014 San Sebastián, Spain.
  • Nahir B; Red de Investigación en Servicios de Salud en Enfermedades Crónicas (REDISSEC), 48960 Galdakao, Spain.
  • Arndt F; Unidad de Gestión Sanitaria, Hospital Alto Deba, 20500 Arrasate-Mondragón, Gipuzkoa, Spain.
  • Dichmann Sorknæs A; School of Engineering, University of Birmingham, Birmingham B15 2TT, UK.
  • Juul NK; Institute of Digital Healthcare, WMG, University of Warwick, Coventry CV4 7AL, UK.
  • Lilja M; School of Engineering, University of Birmingham, Birmingham B15 2TT, UK.
  • Sherman MH; Institute of Digital Healthcare, WMG, University of Warwick, Coventry CV4 7AL, UK.
  • Laleci Erturkmen GB; Digital & Data Driven Research Unit, University Hospitals Coventry & Warwickshire NHS Trust, Clifford Bridge Road, Coventry CV2 2DX, UK.
  • Yuksel M; Assuta Medical Centre Ashdod, Ashdod 7747629, Israel.
  • Robbins T; Assuta Medical Centre Ashdod, Ashdod 7747629, Israel.
  • Kyrou I; Assuta Medical Centre Ashdod, Ashdod 7747629, Israel.
  • Randeva H; Maccabi Healthcare Services Southern Region, Omer 8496500, Israel.
  • Maguire R; Gesunder Werra-Meißner-Kreis GmbH, 37269 Eschwege, Germany.
  • McCann L; Internal Medical & Emergency Department M/FAM, OUH, Svendvorg Hospital, Baagøes Allé 15, Indgang 51, 5700 Svendborg, Denmark.
  • Miller M; Internal Medical & Emergency Department M/FAM, OUH, Svendvorg Hospital, Baagøes Allé 15, Indgang 51, 5700 Svendborg, Denmark.
  • Moore M; Department of Public Health and Clinical Medicine, Unit of Research, Education and Development Östersund, Umeå University, 901 87 Umeå, Sweden.
  • Connaghan J; R&D Project Office, Region Jämtland Härjedalen, 831 30 Östersund, Sweden.
  • Fullaondo A; SRDC, ODTU Teknokent Silikon Blok Kat: 1 No: 16 Cankaya, Ankara 06800, Turkey.
  • Verdoy D; SRDC, ODTU Teknokent Silikon Blok Kat: 1 No: 16 Cankaya, Ankara 06800, Turkey.
  • de Manuel Keenoy E; Digital & Data Driven Research Unit, University Hospitals Coventry & Warwickshire NHS Trust, Clifford Bridge Road, Coventry CV2 2DX, UK.
Article em En | MEDLINE | ID: mdl-36833849
ABSTRACT
Due to population ageing and medical advances, people with advanced chronic diseases (ACD) live longer. Such patients are even more likely to face either temporary or permanent reduced functional reserve, which typically further increases their healthcare resource use and the burden of care on their caregiver(s). Accordingly, these patients and their caregiver(s) may benefit from integrated supportive care provided via digitally supported interventions. This approach may either maintain or improve their quality of life, increase their independence, and optimize the healthcare resource use from early stages. ADLIFE is an EU-funded project, aiming to improve the quality of life of older people with ACD by providing integrated personalized care via a digitally enabled toolbox. Indeed, the ADLIFE toolbox is a digital solution which provides patients, caregivers, and health professionals with digitally enabled, integrated, and personalized care, supporting clinical decisions, and encouraging independence and self-management. Here we present the protocol of the ADLIFE study, which is designed to provide robust scientific evidence on the assessment of the effectiveness, socio-economic, implementation, and technology acceptance aspects of the ADLIFE intervention compared to the current standard of care (SoC) when applied in real-life settings of seven different pilot sites across six countries. A quasi-experimental trial following a multicenter, non-randomized, non-concurrent, unblinded, and controlled design will be implemented. Patients in the intervention group will receive the ADLIFE intervention, while patients in the control group will receive SoC. The assessment of the ADLIFE intervention will be conducted using a mixed-methods approach.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Cuidadores Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Cuidadores Idioma: En Ano de publicação: 2023 Tipo de documento: Article