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The aim of this study is to investigate the feasibility of continuous fever tracking of participants having fever symptoms in a home setting, using a core body temperature (CBT) sensor. CBT as measured by the wearable sensors will be coampared with CBT as measured by ingestible electronc pills (reference).
A secondary research question is, if the CBT behavior of the the participants in a home setting can be compared to previously described CBT profiles in the literature, and if special patterns can be identified.
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Inclusion criteria
Acute fever symptoms at inclusion (at least 38.0°C) and Test for COVID-19 at the day of inclusion
Exclusion criteria
Any participant who, for any reason, is unable to independently consent to participate in the study and/or who is unable to independently follow the study protocol.
Any participant with previous surgical procedures in the gastrointestinal tract
Inability to swallow pills
Any participant of ≤40 kg body weight
A scheduled MRI examination in the period from the start of the measurements until seven days after ingestion of the electronic pill.
Any participant being pregnant
Impairment or disability of the upper extremity likely to have a negative impact on the quality of measurements:
Known allergy to plastics / latex
Language problems
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Data sourced from clinicaltrials.gov
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