A sleep program designed for latino kids aims to close the rest gap
NCT ID NCT06942455
First seen Sep 04, 2026 · Last updated Sep 04, 2026
Summary
This trial tests a sleep education program called SIESTA, designed with urban Latino middle schoolers in mind. Researchers will compare children who receive the sleep program with those who attend general health sessions. Participants wear sleep-tracking watches and fill out surveys to measure sleep duration, quality, and daily impairment. The goal is to see whether a culturally tailored approach can improve sleep health in a group that often faces barriers to good rest.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A culturally tailored sleep hygiene education program called SIESTA, delivered through group sessions and individualized coaching with a parent or guardian.
- What this could lead to
- If it works, this program could offer a practical way to improve sleep health in a group at higher risk for poor sleep, potentially boosting their daily functioning and well-being.
- What could go wrong
- This is a behavioral intervention, so results depend on families sticking with it. The trial is not yet at a large scale, and what works in one urban setting may not translate to others.
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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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About 300 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2025
- Expected to finish
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Mar 2029
An estimate. End dates often move.
- 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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11 to 13 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * children must be middle schoolers between 11-13 years old, live and go to school in one of the targeted school districts and sleep no more than 9 hours on an average night Exclusion Criteria: * Children are not eligible to take part in the study if they have a medical, psychiatric, or developmental condition and/or are taking medicine for any condition that might affect their ability to and comfort with taking part in the study.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites in 2 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Centro Medico
NOT_YET_RECRUITINGSan Juan, Puerto Rico, Puerto Rico
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Rhode Island Hospital
RECRUITINGProvidence, Rhode Island, 02903, United States
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