Assessment of the Effectiveness, Socio-Economic Impact and Implementation of a Digital Solution for Patients with Advanced Chronic Diseases: The ADLIFE Study Protocol

Author:

García-Lorenzo Borja1,Gorostiza Ania1ORCID,González Nerea12,Larrañaga Igor1,Mateo-Abad Maider13ORCID,Ortega-Gil Ana1ORCID,Bloemeke Janika4ORCID,Groene Oliver4ORCID,Vergara Itziar3,Mar Javier15678ORCID,Lim Choi Keung Sarah N.910ORCID,Arvanitis Theodoros N.91011ORCID,Kaye Rachelle12,Dahary Halevy Elinor12,Nahir Baraka1213,Arndt Fritz14ORCID,Dichmann Sorknæs Anne15ORCID,Juul Natassia Kamilla15,Lilja Mikael16ORCID,Sherman Marie Holm17,Laleci Erturkmen Gokce Banu18ORCID,Yuksel Mustafa18ORCID,Robbins Tim11ORCID,Kyrou Ioannis11ORCID,Randeva Harpal11,Maguire Roma19,McCann Lisa19,Miller Morven19,Moore Margaret19,Connaghan John19ORCID,Fullaondo Ane1ORCID,Verdoy Dolores1ORCID,de Manuel Keenoy Esteban1ORCID

Affiliation:

1. Kronikgune Institute for Health Services Research, Ronda de Azkue 1, Torre del Bilbao Exhibition Centre, 48902 Barakaldo, Basque Country, Spain

2. Osakidetza Basque Health Service, Barrualde-Galdakao, Integrated Health Organisation, 48960 Galdakao, Spain

3. Biodonostia Health Research Institute, Paseo Dr. Begiristain s/n, 20014 Donostia, Basque Country, Spain

4. OptiMedis, Burchardstrasse 17, 20095 Hamburg, Germany

5. Unidad de Investigación AP-OSIs, Hospital Alto Deba, 20500 Arrasate-Mondragón, Gipuzkoa, Spain

6. Instituto de Investigación Sanitaria Biodonostia, 20014 San Sebastián, Spain

7. Red de Investigación en Servicios de Salud en Enfermedades Crónicas (REDISSEC), 48960 Galdakao, Spain

8. Unidad de Gestión Sanitaria, Hospital Alto Deba, 20500 Arrasate-Mondragón, Gipuzkoa, Spain

9. School of Engineering, University of Birmingham, Birmingham B15 2TT, UK

10. Institute of Digital Healthcare, WMG, University of Warwick, Coventry CV4 7AL, UK

11. Digital & Data Driven Research Unit, University Hospitals Coventry & Warwickshire NHS Trust, Clifford Bridge Road, Coventry CV2 2DX, UK

12. Assuta Medical Centre Ashdod, Ashdod 7747629, Israel

13. Maccabi Healthcare Services Southern Region, Omer 8496500, Israel

14. Gesunder Werra-Meißner-Kreis GmbH, 37269 Eschwege, Germany

15. Internal Medical & Emergency Department M/FAM, OUH, Svendvorg Hospital, Baagøes Allé 15, Indgang 51, 5700 Svendborg, Denmark

16. Department of Public Health and Clinical Medicine, Unit of Research, Education and Development Östersund, Umeå University, 901 87 Umeå, Sweden

17. R&D Project Office, Region Jämtland Härjedalen, 831 30 Östersund, Sweden

18. SRDC, ODTU Teknokent Silikon Blok Kat: 1 No: 16 Cankaya, Ankara 06800, Turkey

19. Department of Computing and Information Sciences, University of Strathclyde, Glasgow G1 1XQ, UK

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.

Funder

European Commission

Publisher

MDPI AG

Subject

Health, Toxicology and Mutagenesis,Public Health, Environmental and Occupational Health

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