The Sleep Initiative is a non-profit organization, officially recognized as a Social and Solidarity Economy (SSE) actor, whose mission is to simplify sleep care pathways in France and across Europe by providing healthcare professionals with free, sovereign digital tools.
Explore ProjectsNeed to explain a PV or PSG? Answer frequently asked questions about CPAP? Convey sleep hygiene habits? It's all so easy with pre-set text messages: just enter the phone number, select the message(s) and voilà.
Your patient receives everything directly on their phone: videos to click, questionnaires to fill, a link to your website. The server is unidirectional — no replies.
• Doctors: refer your insomnia patients in less than 10 seconds, to a referral center, a specialized psychologist in private practice or an online therapy.
• Insomnia psychologists: manage all inclusions, reminders, questionnaires and appointments in 1 clear and intuitive page.
Your administrative time is reduced by 90%. Managing insomnia has never been easier.
A prescription and coordination platform for diagnostic tests, hosted on an HDS-accredited server. Delegate sleep assessments to your technicians while maintaining full supervision and ensuring patient safety at every step.
Collect structured patient data before consultations. Prioritize cases efficiently, support clinical research initiatives, and generate actionable statistics to continuously improve your practice.
To help everyone really care more, we aim to optimize transdisciplinarity in sleep and somnopathy care paths. Our tools include not only doctors, but also sleep technicians, psychologists and administrative functions. Include your teams and partners in 1 click.
A streamlined web interface — nothing to install. Communication by e-mail and SMS to reach all populations, including multi-language subtitled videos. For too long, medicine has been at war with IT. Let's change that.
Saving time and comfort is our collective challenge, but not at the cost of a monetized private life. The association and its partners have no access to clinical data. Access will only be granted to legitimate clinical trial coordinating centers for public research purposes.
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