Snore Quell Patient Experience STUDY

200 participants — medical professionals, patients and partners

Contact:
Dave Joffe, Editor-in-Chief
Phone 727-224-4347
editor@diabetesincontrol.com

The purpose of this experience study is to determine if the above mentioned product can reduce or eliminate snoring.

We have focused on diabetes patients, family members, and medical professionals based on information from an article in the American Journal of Epidemiology Vol. 155, No. 5 : 387-393, which stated, “Snoring is independently associated with the elevated risk of Type 2 Diabetes.”

In addition recent research and anecdotal evidence has shown that interruption of normal sleep patterns can cause disruptions in early morning glucose levels.

This Experience study is not being used to evaluate changes in blood glucose readings and does not require any extra testing.

The Experience Study will evaluate the effectiveness of the SnoreQuell product in decreasing or eliminating snoring. This will be determined by comparing before and after questionnaires to be completed by each participant.

See Initial Survey Form Here    See Follow-up Survey Form Here

This study will last for 30 days.

If a significant number of participants have positive results, we will conclude that this product is effective in reducing or eliminating snoring.


Registration:
At this time we are seeking medical professionals who will administer the product to 5 participants including themselves, patients or partners of patients. Fill out the form below to enroll.

(if you are not a medical professional and wish to participate, please email us at diabetes@tampabay.rr.com )

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