A Sleep Hygiene Intervention to Improve Sleep Quality in Urban, Latino Middle School Children - Phase 2
NCT ID: NCT03717246
Last Updated: 2021-04-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
90 participants
INTERVENTIONAL
2021-02-12
2021-09-30
Brief Summary
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Detailed Description
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The first aim of this project is to refine the SS intervention and intervention procedures so that they eventually can be used in a larger study of the intervention's effectiveness. Refinement will involve a) translation and cultural tailoring for Latino middle school students, b) enhancement of the parent component, and c) ensuring applicability to the urban, middle school setting in both sites (PR and RI). In-depth interviews with caregivers (N=20-25), focus groups (middle school students \[N = 5\], caregivers \[N =5\], and school staff \[N = 5\]), and Investigators with expertise in culturally tailored interventions will provide input.
The second aim of this application is to test the feasibility of the SSL intervention and training procedures through an Open Trial, to refine intervention modules and the training approach that will be used in the larger study. The Open Trial will include 15 adolescent participants at each study site.
The third aim of this application is to test the SSL intervention through a Pilot Randomized Control Trial to provide estimates of effect size that will be used to inform the sample size for the larger study. The RCT will include 75 adolescent participants at each study site. We expect the participants in the SSL intervention will have improvement on the following primary sleep quality outcomes (improved sleep duration and sleep efficiency) as measured by actigraphy, relative to the control conditions. Secondarily, we expect participants in SSL will show a decrease in total daily caloric intake relative to the control conditions.
This registration refers only to aims 2 and 3 of the project.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Sleep Smart Latino
Sleep Smart Latino is a sleep hygiene intervention culturally tailored to be consistent with the beliefs, behaviors and needs of urban Latino middle school children and families. It consists of 4 60-minute sessions delivered in a group format in an urban middle school setting, and 2 60-minute long home based sessions that involve the student and their caregiver. The intervention focuses on sleep education, including effective sleep hygiene practices, use of electronics and caffeine and their impact on sleep.
Sleep Smart Latino
A culturally tailored group intervention aimed at improving sleep duration and quality for Latino middle school students.
Basic Sleep Education and Child Health
The basic sleep education and child health condition includes education regarding sleep hygiene , and the effects of sleep on child functioning integrated with additional child health topics such as nutrition, physical activity and safety. It consists of 4 60-minute sessions delivered in a group format in an urban middle school setting
Basic Sleep Hygiene and Child Health
A group intervention providing sleep hygiene and child health topics education to Latino middle school students.
No treatment control
Students randomly assigned to this arm, will receive standard of care , which is no treatment and will not participate in any group sessions.
No interventions assigned to this group
Interventions
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Sleep Smart Latino
A culturally tailored group intervention aimed at improving sleep duration and quality for Latino middle school students.
Basic Sleep Hygiene and Child Health
A group intervention providing sleep hygiene and child health topics education to Latino middle school students.
Eligibility Criteria
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Inclusion Criteria
1. be between the ages of 11-13,
2. be in 6th-8th grades,
3. reside in one of the targeted public school districts identified by zip code,
4. attend one of the schools within these districts, and
5. have sleep duration \< 9 hours
Exclusion Criteria
2. current/prior sleep disorder diagnosis, such as sleep disordered breathing, restless leg syndrome, or periodic limb movement disorder (PLMD)
11 Years
13 Years
ALL
Yes
Sponsors
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University of Puerto Rico
OTHER
Rhode Island Hospital
OTHER
Responsible Party
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Principal Investigators
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Daphne Koinis-Mitchell, PhD
Role: PRINCIPAL_INVESTIGATOR
Rhode Island Hospital
Glorisa Canino, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Puerto Rico
Maria T Coutinho, PhD
Role: STUDY_DIRECTOR
Rhode Island Hospital
Locations
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Rhode Island Hospital
Providence, Rhode Island, United States
University of Puerto Rico
San Juan, , Puerto Rico
Countries
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Central Contacts
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Facility Contacts
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Glorisa Canino, PhD
Role: primary
Other Identifiers
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1R34HL135073 -Phase 2
Identifier Type: -
Identifier Source: org_study_id
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