Investigation of Fatigue Using Digital Technologies
Résumé de l'étude
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)
Intervention étudiée
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)
Maladie en cours d'investigation
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)
Critères d'exclusion
- Consent after information not possible.
- Not willing or unable to comply with the study protocol.
- Pregnancy or breastfeeding.
- Diagnosis of other chronic diseases.
(BASEC)
Lieu de l’étude
Bâle, Zurich
(BASEC)
Sponsor
University of Zurich
(BASEC)
Contact pour plus d'informations sur l'étude
Personne de contact en Suisse
Dr. sc. Liliana Barrios
+41774141174
fido@clutterdsi.uzh.chUniversity of Zurich
(BASEC)
Informations scientifiques
non disponible
Nom du comité d'éthique approbateur (pour les études multicentriques, uniquement le comité principal)
Commission cantonale de Zurich
(BASEC)
Date d'approbation du comité d'éthique
21.03.2025
(BASEC)
Identifiant de l'essai ICTRP
non disponible
Titre officiel (approuvé par le comité d'éthique)
Fatigue Investigation using Digital Outcomes (FIDO) - an exploratory project (BASEC)
Titre académique
non disponible
Titre public
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Maladie en cours d'investigation
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Intervention étudiée
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Type d'essai
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Plan de l'étude
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Critères d'inclusion/exclusion
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Critères d'évaluation principaux et secondaires
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Date d'enregistrement
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Inclusion du premier participant
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Sponsors secondaires
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Contacts supplémentaires
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ID secondaires
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Résultats-Données individuelles des participants
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Informations complémentaires sur l'essai
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Résultats de l'essai
Résumé des résultats
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Lien vers les résultats dans le registre primaire
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