The Influence of Sleep and Stress on Migraine
Summary description of the study
Project Summary In the MiSleepS study, we investigate how sleep disorders and stress are related to migraine attacks. Participants wear a device (WHOOP band) that measures sleep and body data and answer short daily questions about sleep, stress, and migraine through a smartphone app. The goal is to identify personal patterns that may contribute to migraines. Based on these insights, participants receive individualized recommendations to improve their sleep and daily life – aiming to reduce migraine attacks in the long term and without medication. The study is conducted at the University Hospital Zurich and targets adults with episodic migraine.
(BASEC)
Intervention under investigation
Targeted improvement of sleep and stress reduction (non-medication)
(BASEC)
Disease under investigation
Migraine (Headache)
(BASEC)
Adults aged 18-65 with diagnosed migraine who had between 4-14 headache days per month in the 3 months prior to inclusion. (BASEC)
Exclusion criteria
Severe known sleep disorder (such as obstructive sleep apnea), severe psychiatric illness, use of medications affecting sleep structure such as benzodiazepines. (BASEC)
Trial sites
Zurich
(BASEC)
Sponsor
PI is the sponsor
(BASEC)
Contact
Contact Person Switzerland
Prof. Dr. Susanne Wegener
044 255 1111
Susanne.Wegener@clutterusz.chKlinik für Neurologie, Universitätsspital Zürich (USZ)
(BASEC)
Scientific Information
not available
Name of the authorising ethics committee (for multicentre studies, only the lead committee)
Ethics Committee Zurich
(BASEC)
Date of authorisation
09.09.2025
(BASEC)
ICTRP Trial ID
not available
Official title (approved by ethics committee)
Migraine Sleep Study (MiSleepS) (BASEC)
Academic title
not available
Public title
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Disease under investigation
not available
Intervention under investigation
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Type of trial
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Trial design
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Inclusion/Exclusion criteria
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Primary and secondary end points
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Registration date
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Incorporation of the first participant
not available
Secondary sponsors
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Additional contacts
not available
Secondary trial IDs
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Results-Individual Participant Data (IPD)
not available
Further information on the trial
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Results of the trial
Results summary
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Link to the results in the primary register
not available