Feasibility of Wearable-Based Continuous Temperature Monitoring
ConditionTemperature Change, Body
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Basel, Switzerland
About this trial
The aim of this study is to evaluate the feasibility of collecting synchronised continuous temperature data using wearable devices and a continuous core temperature reference under real-world conditions. The study focuses on workflow execution, data continuity, secure retrieval, and time-alignment without diagnostic or therapeutic intent.
Eligibility criteria
Qualifiers
Written informed consent obtained prior to any project-specific procedures.
Age 18 years or older at enrolment.
Able and willing to comply with project procedures, including capsule ingestion, continuous wearable use for around 48 hours, and adherence to study instructions.
Able to swallow the ingestible temperature capsule without difficulty.
Disqualifiers
Body weight < 36 kg.
Women who are pregnant.
Participation in another clinical investigation involving an investigational medicinal product or medical device within the 30 days preceding enrolment or previous enrolment in the current project.
Enrolment of the Principal Investigator, project staff, their family members, employees, or other dependent persons.
Trial design
Treatments tested in this trial
- Continuous Temperature Monitoring
Treatment groups
12 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov