Cool your head, sleep better? new study tests a pillow pad for Weight-Related sleep problems
NCT ID NCT05849181
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested whether a special cooling pillow pad called Moona can help African American adults with overweight or obesity sleep better. 18 participants used either the active cooling pad or an inactive version for 22 days. Researchers measured sleep quality, timing, and blood sugar control to see if the device made a difference.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Moona Device (cooling pillow pad)
- What this could lead to
- If it works, this could point toward a simple, non-drug way to improve sleep and metabolism in people with overweight or obesity.
- What could go wrong
- This is a very small pilot study with only 18 participants, so results may not apply to everyone. The device is not a treatment for obesity itself.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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18 people
The number who actually took part.
- Started
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Mar 2024
- Finished
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Aug 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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21 to 50 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * African American men and women * Aged 21-50 years * BMI ≥ 27 to 45 kg/m2 * Self-report of short or poor sleepers (\>5 \< 7hrs /night and/or a score \> 5 on the PSQI), * Sleeping between 22:00 and 08:00. * Ability to provide informed consent before any trial-related activities * Controlled hypertension or dyslipidemia. Exclusion Criteria: * Previous diagnosis or reveled during the screening PSG (Polysomnography) of obstructive sleep apnea (AHI≥30) or other sleep disorders based on DSM-V (Diagnostic and Statistical Manual of Mental Disorders, fifth edition) criteria. * Shift work * Diagnosis of diabetes based on history or screening tests * History of cognitive or other neurological disorders * History of major psychiatric disorder based on DSM-V criteria * Presence of unstable or serious medical conditions * Use within the past month of melatonin, psychoactive, hypnotic, stimulant or pain medications (except occasionally) * Caffeine consumption of greater than 500 mg per day * Medically managed weight loss program within the past 6 months * History of bariatric weight loss surgery. * Women who are pregnant, plan on becoming pregnant, are breastfeeding, * Men or women who have a child at home that does not sleep through the night. * Active drug/alcohol dependence or abuse
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Chicago
Chicago, Illinois, 60637, United States
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