Circadian Sleep Disorders Network is sponsoring a PATIENT POWERED REGISTRY AND SURVEY for people with Circadian Rhythm Sleep Disorders. The registry is open to anyone with a circadian rhythm sleep disorder from any country. You can sign up for the registry and take the survey (it's free) at https://connect.altavoice.org/?org=CSD-N.
By collecting health information from as many people as possible, together we can make a difference. We can:
The registry and survey are hosted by AltaVoice (formerly Patient Crossroads), now a subsidiary of Invitae. AltaVoice provides compliance with HIPAA (U.S. Health Insurance Portability and Accountability Act) privacy requirements. They assure you that you own your data, and that no one can identify you without your permission. They refer to the registry and survey as a "Patient Insight Network" (PIN). Here's an AltaVoice video describing it.
They host similar PINs for 100 organizations representing 400 diseases. Other clients include the U.S. National Institutes of Health (NIH) and the U.S. Patient-Centered Outcomes Research Institute (PCORI).
Note that your information is de-identified: anyone accessing the survey responses does not know whose responses they are. To be contacted by researchers you must first agree to be contacted by AltaVoice for research; and subsequently, if a researcher requests AltaVoice to contact people with certain responses, AltaVoice will request you to contact the researcher. Your name and contact information are not given out without your explicit permission.
By working together and sharing information, we can transform medicine in ways that were unimaginable a decade ago. Your participation may result in new therapies, while rapidly increasing our knowledge of disordered circadian processes.
The information you provide can jump-start research on some of the questions we've been asking about for years - but only if enough people participate. Sign up now (free), and please take the survey.
Questions? Problems? Contact us at .
And please consider joining Circadian Sleep Disorders Network, if you haven't already done so.
I think of a rare disease registry as a tool for research.... Part of the reason for a rare disease registry in the early stage of research is proof of concept. An advocacy group is able to demonstrate to a clinical researcher that it has a legitimate population and carefully collected data and consent from patients to review their data, among other benefits. The registry essentially provides evidentiary material and justification for a research study.
--Catherine Olson, CoRDS, Global Genes
Insights from registries may result in new approaches to research by uncovering common traits, behaviors, and symptoms that may guide researchers into areas that they had not previously considered. These insights may also change the standard of care for patients. For instance, if we know that many people with a certain rare disease are struggling with a previously unrecognized condition that can be presented to medical specialists and change the standard of care for that disease.
--Global Genes, The Purpose of a Registry
The registry provides us with vital ammunition in the ongoing battle with medical professionals unfamiliar with rare disorders, or with the 'powers that be' in the local school system where educators often refuse to provide one-one assistance. Suddenly you are not some crazy mom making outrageous demands for extra care or special education services or one-on-one supervisory assistance. Instead, you are a concerned parent communicating undeniable research findings.
--Megan O'Boyle, Global Genes
Rare disease registries can play a vital role in providing researchers new insights into rare diseases that can help lead to earlier diagnosis, improved care, and new therapies.
--Global Genes, Conclusion
It would be beneficial for future etiological DSPD investigations to present clear, well-defined lifestyle factors, symptoms and inclusion criteria used to classify DSPD samples.... Such screening data may help to identify predictors and mechanisms driving various subtypes of DSPD. This information could further be used to obtain severity index measures.
--Micic et al, The etiology of delayed sleep phase disorder
Delayed Sleep Phase Disorder (DSPD). Sleep occurs later than desired, but usually at around the same time every day (within a few hours). To get enough sleep, one needs to sleep late into the morning or afternoon. Waking up earlier is difficult. The body is resistant to shifting the schedule earlier with the usual sleep hygiene methods. (Other names include Delayed Sleep Phase Syndrome (DSPS), Circadian Rhythm Sleep Disorder – Delayed Phase Type, and similar.)
Non-24-Hour Sleep-Wake Disorder (Non-24). Sleep occurs later and later each day, progressing all the way around the clock. In some persons living on a 24 hour schedule, Non-24 may present as periods of insomnia recurring at regular intervals over weeks or months. (Other names include Free Running Disorder, Hypernychthemeral Syndrome, Circadian Rhythm Sleep Disorder – Free Running Type, and similar.)
Advanced Sleep Phase Disorder (ASPD). Sleep occurs earlier than desired, and the sleeper has difficulty staying up in the evening and wakes up very early. (Other names include Advanced Sleep Phase Syndrome (ASPS), Circadian Rhythm Sleep Disorder – Advanced Phase Type, and similar.)
Irregular Sleep-Wake Disorder (ISWD). Sleep is not regular, and generally there are multiple sleep periods each day. (Other names include Circadian Rhythm Sleep Disorder – Irregular Type, and similar.)
Circadian Rhythm Sleep Disorder (CRSD). Any of the above four disorders. (Also Circadian Rhythm Disorder (CRD))
We are not surveying shift work disorder, which likely has different underlying causes.
Questions? Problems? Contact us at .