Investigation of Fatigue Using Digital Technologies
Descrizione riassuntiva dello studio
The aim of this exploratory study is to assess the feasibility of long-term fatigue monitoring based on compliance rates for the use of wearable devices and the completion of app tasks. This assessment will show whether the approach has the potential for future monitoring of MS and Long-COVID patients.
(BASEC)
Intervento studiato
Your participation is required for two months and includes two clinic visits and a data collection phase:
- Preparation at home: You will receive the consent form for the study (this document) and the user manuals.
- First study visit: You will sign the consent form together with the study team. You will undergo a medical examination, fill out questionnaires, and become familiar with the digital technologies of the study. The study visit lasts about two hours.
- Data collection phase: You will continuously wear two wearable devices for two months (24/7), charge them regularly, and download the data. Additionally, you will use the FIDO app to perform short tasks (about 7 minutes every two days) and fill out short questionnaires at regular intervals (~5 minutes per day). The app is intuitive and self-explanatory and will send you notifications to remind you of the tasks. Additionally, after 4 and 8 weeks, you should collect a stool sample at home for an analysis of your gut bacteria and fill out two questionnaires.
- Last study visit: After the two months, you will visit the clinic again for a second medical examination and provide feedback on the digital technology. You will also return the devices. The study visit lasts 60 to 90 minutes.
(BASEC)
Malattie studiate
Fatigue in Healthy Individuals and MS & Long COVID Patients
(BASEC)
MS or Long-COVID Patient Group:
- Confirmed diagnosis of MS (by a neurologist) or Long-COVID (by a doctor)
- Adults aged between 18 and 65 years.
- Participants should own a smartphone. The smartphone should have at least iOS version 16 (available from iPhone 8) or Android version 10.
- Fluent in German or English.
Control Group:
- Adults aged between 18 and 65 years.
- Ownership of a smartphone. The smartphone should have at least iOS version 16 (available from iPhone 8) or Android version 10.
- Fluent in German or English.
(BASEC)
Criteri di esclusione
- Consent after information not possible.
- Not willing or unable to comply with the study protocol.
- Pregnancy or breastfeeding.
- Diagnosis of other chronic diseases.
(BASEC)
Luogo dello studio
Basilea, Zurigo
(BASEC)
Sponsor
University of Zurich
(BASEC)
Contatto per ulteriori informazioni sullo studio
Persona di contatto in Svizzera
Dr. sc. Liliana Barrios
+41774141174
fido@clutterdsi.uzh.chUniversity of Zurich
(BASEC)
Informazioni scientifiche
non disponibile
Nome del comitato etico approvante (per studi multicentrici solo il comitato principale)
Commissione etica Zurigo
(BASEC)
Data di approvazione del comitato etico
21.03.2025
(BASEC)
ID di studio ICTRP
non disponibile
Titolo ufficiale (approvato dal comitato etico)
Fatigue Investigation using Digital Outcomes (FIDO) - an exploratory project (BASEC)
Titolo accademico
non disponibile
Titolo pubblico
non disponibile
Malattie studiate
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Intervento studiato
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Tipo di studio
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Disegno dello studio
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Criteri di inclusione/esclusione
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Endpoint primari e secondari
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Data di registrazione
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Inclusione del primo partecipante
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Sponsor secondari
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Contatti aggiuntivi
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ID secondari
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Risultati-Dati individuali dei partecipanti
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Ulteriori informazioni sullo studio
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Risultati dello studio
Riepilogo dei risultati
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Link ai risultati nel registro primario
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