Cardiovascular and Applied Physiology Laboratory
Tallahassee, Florida, 32306, United States
NCT Number: NCT06403098
The goal of this interventional study is to learn if wearing an external nasal dilator strip while sleeping changes objective and perceived sleep quality, immediate post-waking blood pressure, and immediate-post waking heart rate variability.
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Notify Me18 year–30 year
All sexes
Interventional
Not applicable
Tallahassee, Florida, 32306, United States
Nasal dilator strips are strips often made up of stiff plastic, placed on the lower bridge of the nose by an adhesive strip. They work by slightly pulling the nostrils and surrounding nose bridge area outward, dilating the nostrils, and decreasing air resistance. Nasal breathing is associated with lower diastolic blood pressure, an important marker of heart health, in comparison to mouth breathing. In addition to blood pressure, nasal breathing during sleep is potentially related with better sleep quality. Participating in this study will help us understand the effect nasal dilator strips have on cardiovascular and sleep health. Better understanding of the benefits of nasal dilator strips will provide important knowledge to researchers who study how the body works.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will wear an extra strength Breathe Right nasal strip overnight.
Time frame: Immediate post-waking for 14 consecutive days. Weekly averages (e.g. day 1-7 vs 8-14) will be compared between conditions.
Brachial systolic blood pressure will be measured with an automated blood pressure monitor (OMRON BP5250).
Time frame: Immediate post-waking for 14 consecutive days. Weekly averages (e.g. day 1-7 vs 8-14) will be compared between conditions.
Brachial diastolic blood pressure will be measured with an automated blood pressure monitor (OMRON BP5250).
Time frame: Immediate post-waking for 14 consecutive days. Weekly averages (e.g. day 1-7 vs 8-14) will be compared between conditions.
Heart rate variability will be measured with a Polar H10 and the Elite-HRV mobile application.
Time frame: Immediate post-waking for 14 consecutive days. Weekly averages (e.g. day 1-7 vs 8-14) will be compared between conditions.
Heart rate will be measured with a Polar H10 and the Elite-HRV mobile application.
Time frame: During sleep for 14 consecutive days (7 per condition).
Wrist-based actigraphy outcome during sleep tracking.
Time frame: Immediate post-waking for 14 consecutive days (7 per condition).
Self-rated sleep quality on a 5-point Likert scale (1=very poor, 5=very good.
Florida State University
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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