A Sleep Hygiene Intervention to Improve Sleep Health in Urban, Latino Middle School Children
Rhode Island Hospital · with National Institute on Minority Health and Health Disparities (NIMHD), University of Puerto Rico · NCT06942455
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 11–13 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 300
- US sites recruiting
- 1
- Study start
- June 25, 2025
- Record last updated
- September 4, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The main goal of this study is to evaluate the "SIESTA" intervention, a culturally and contextually tailored sleep hygiene intervention that has the potential to exert greater improvements in sleep hygiene and sleep outcomes for group that may be more vulnerable to poor sleep health.
The main question is: do SIESTA participants have improved sleep outcomes, sleep hygiene behaviors and less sleep-related impairment compared to Control Group participants?
Participants randomized to the SIESTA intervention will:
- Attend 4 remotely administered group sleep hygiene education sessions
- Complete along with a parent/guardian, two individualized sessions administered by a SIESTA intervention facilitator
- Complete study survey at baseline, end of treatment, and at 4, 8 and 12 months post-intervention.
- Wear electronic sleep watches (actigraphy) throughout the protocol to objectively measure sleep duration and quality.
Participants randomized to the Child Health Control condition will:
- Attend 4 remotely administered group sessions covering general health topics
- Complete along with a parent/guardian, two individualized sessions administered by a SIESTA intervention facilitator
- Complete study survey at baseline, end of treatment, and at 4, 8 and 12 months post-intervention.
- Wear electronic sleep watches (actigraphy) throughout the protocol to objectively measure sleep duration and quality.
A secondary goal of the study is to conduct a process evaluation to prepare for future larger scale use of the intervention in other urban school settings. This will entail assessing Reach, Effectiveness, Adoption, Implementation, and Maintenance (RE-AIM) of the program through several methods, such as by conducting in-depth interviews with research participants and their parents/guardians, as well as school staff and by looking at rates of participation in the program.
Being studied: SIESTA; Sleep education and health education control
Conditions: Sleep; Sleep Quality; Intervention Study; Ethnic Minority
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
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.
Recruiting US locations
Rhode Island Hospital
Providence, RI 02903
Site contact: Sheryl J Kopel, MSc · +1-401-444-7217 · sjkopel@brownhealth.org
Study contacts (from the official record)
- Sheryl J Kopel, MSc · +1-401-444-7217 · Sheryl_Kopel@brown.edu
- Daphne Koinis-Mitchell, PhD · +1-401-793-8632 · Daphne_Koinis-Mitchell@brown.edu
Similar studies in Rhode Island
All sleep studies in Rhode Island →- RecruitingPhase 3
A Study of Suvorexant (MK-4305) for the Treatment of Insomnia Disorder in Participants With Opioid Use Disorder (MK-4305-098)
Merck Sharp & Dohme LLC
- Location
- Providence, RI + 12 other US sites
- Eligibility basics
- Ages 18–70
- RecruitingPhase 3
A Phase 3 Efficacy and Safety Study of HBS-301 in Participants With Idiopathic Hypersomnia (IH)
Harmony Biosciences Management, Inc.
- Location
- East Providence, RI + 39 other US sites
- Eligibility basics
- Ages 18+
- RecruitingHealthy volunteers
The Dream Team: Testing Implementation of a Sleep Intervention for Perinatal Women Delivered by Direct Care Workers
Rhode Island Hospital
- Location
- Providence, RI
- Eligibility basics
- Ages 18–99