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The UpcomingVoice project aims to co-design a digital health solution based on vocal biomarkers for screening and self-monitoring of frequently reported COVID-19-related symptoms with its end-users: 1) people with persisting COVID-19 related symptoms, with or without a Long COVID diagnosis and 2) healthcare professionals involved in the care of Long COVID patients.
To achieve this objective the UpcomingVoice study will determine:
The project consists in 2 separate parts : one anonymous online survey and one qualitative part based on semi-structured interviews and focus groups.
The results of this study will be the specifications of a voice-based digital health solution.
Full description
The COVID-19 pandemic accelerated the use of remote patient monitoring in clinical practice or research for safety and emergency reasons, justifying the need for innovative digital health solutions to monitor key parameters or symptoms related to COVID-19 or Long COVID. A panel of experts from the National Institute for Health and Care Excellence (NICE) recommended the development of telemonitoring and encouraged self-management of acute and Long COVID symptoms in a tailored and accessible way for each patient.
Voice is an interesting approach to use for telemonitoring as it is easy-to-collect, quick, energy efficient, and inducing less burden for patients. To bring vocal biomarkers of different symptoms into clinical and real-life practice, they have to be implemented in a digital health solution, for example a smartphone application.
It is crucial to involve the end-users in the development of such a digital health solution and in this project involve them during the entire project course.
The study protocol, the participant's documents, and the questionnaires have been reviewed by both Long COVID patients and HCPs prior to submission.
The co-design process will consist in 3 steps, each involving both patients and HCPs:
The project is based on a mixed methods study and will integrate both qualitative and quantitative methods. Participants will be invited to participate in:
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Inclusion Criteria:
125 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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