2022
DOI: 10.1177/20552076221134448
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User experience reevaluation and diffusion of technology in the context of compulsory usage illustrated by the example of telepsychotherapy—a literature review

Abstract: Objective Models explaining technology acceptance fail to recognize the influence temporary, compulsory usage, meaning forced usage due to external factors, may have on user evaluation and continued diffusion. However, in context of the Covid-19 pandemic, a highly infectious respiratory disease, the significance of this factor is evident. Triggered by legal contact restrictions and extended reimbursement capacities, usage of telepsychotherapy increased drastically, thereby influencing therapists' attitude and … Show more

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Cited by 2 publications
(11 citation statements)
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References 30 publications
(209 reference statements)
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“…An important uptake factor of digital therapeutics was the presence of a legal framework to (1) distinguish digital therapeutics from commercial lifestyle and well-being apps, accrediting the former as a reimbursable form of health care, and (2) protect patients’ privacy, confidentiality, and (health) data security [ 1 , 4 , 5 , 13 , 15 , 47 , 52 , 54 - 56 , 59 , 66 , 77 , 80 , 87 , 96 , 99 , 108 , 109 , 112 , 116 , 120 , 123 , 133 , 139 , 148 , 149 , 157 , 161 , 166 , 167 , 169 , 186 , 190 , 208 , 209 , 212 , 231 ]. A clear example of such a legal framework is the mHealthBelgium validation pyramid in Belgium, which consists of 3 levels: the first level determines the basic requirements, such as the need for Conformité Européene marking, which indicates that a product adheres to the European Union health, safety, and environmental protection standards; the second level is designed to ensure interoperability and connectivity with the broader health informatics system; and the third level regulates the funding of digital health apps by the National Institute of Health and Disability Insurance, which is acquired after a digital health app has passed the clinical review process [ 224 ].…”
Section: Resultsmentioning
confidence: 99%
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“…An important uptake factor of digital therapeutics was the presence of a legal framework to (1) distinguish digital therapeutics from commercial lifestyle and well-being apps, accrediting the former as a reimbursable form of health care, and (2) protect patients’ privacy, confidentiality, and (health) data security [ 1 , 4 , 5 , 13 , 15 , 47 , 52 , 54 - 56 , 59 , 66 , 77 , 80 , 87 , 96 , 99 , 108 , 109 , 112 , 116 , 120 , 123 , 133 , 139 , 148 , 149 , 157 , 161 , 166 , 167 , 169 , 186 , 190 , 208 , 209 , 212 , 231 ]. A clear example of such a legal framework is the mHealthBelgium validation pyramid in Belgium, which consists of 3 levels: the first level determines the basic requirements, such as the need for Conformité Européene marking, which indicates that a product adheres to the European Union health, safety, and environmental protection standards; the second level is designed to ensure interoperability and connectivity with the broader health informatics system; and the third level regulates the funding of digital health apps by the National Institute of Health and Disability Insurance, which is acquired after a digital health app has passed the clinical review process [ 224 ].…”
Section: Resultsmentioning
confidence: 99%
“…It was emphasized that there were benefits to allowing the procurement of digital therapeutics as locally as possible, as health purchasers (eg, Integrated Care Boards in the United Kingdom, insurance companies in the Netherlands, and employer groups in the United States) are best placed to assess the needs and preferences of their covered population, although this could translate into longer adoption times and higher uptake costs, as each individual insurer needs to invest in the digital infrastructure. There was a stated need to adjust or redesign the existing protocols and professional guidelines, commonly created for the provision of face-to-face health care, to create opportunities for digital therapeutics and address the liability and risk-sharing concerns with using digital therapeutics [ 19 , 51 , 52 , 57 , 63 - 66 , 81 , 87 , 106 , 110 , 112 , 114 , 118 , 121 , 126 , 139 , 149 , 158 , 192 , 205 , 207 , 225 , 233 ]. The presence or development of a high-quality digital infrastructure that can be accessed by all population groups [ 1 , 5 , 13 , 40 , 45 , 47 , 63 , 66 , 74 , 87 , 100 , 106 , 119 , 122 , 124 , 134 , 135 , 137 , 140 , 153 , 162 , 199 , 201 , 209 , 218 , 238 , 270 , 273 ], the availability of testing environments so that health professionals can gain experience with digital therapeutics [ …”
Section: Resultsmentioning
confidence: 99%
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