Optimizing the Timing of rTMS to Enhance the Administration of Insomnia Treatment
Recruiting
N/A
Interventional Study
Insomnia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 25 – 45
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 10 (estimated)
- Sponsor
- Stanford University · Other
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About This Trial
Repetitive transcranial magnetic stimulation (rTMS) has shown to be a promising technique for improving insomnia symptoms and sleep quality. However, the impact of circadian rhythmicity on rTMS sessions and its potential influence on insomnia therapy remains unclear. Moreover, the effect of rTMS on objective sleep parameters is not fully established. The objective of this pilot study is to establi…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Males and females of any racial or ethnic group, aged 25-45 (inclusive)
* Insomnia diagnosis via the DUKE
* Fluent and literate in English
* Written, informed consent
* Reside within 60 miles of Stanford University
Exclusion Criteria:
* Presence of other sleep or circadian r…
Contacts