N/A
Completed N=1,095
Reopening Schools Safely and Educating Youth Research Study (ROSSEY)
Absenteeism
Source: ClinicalTrials.gov NCT04859699 ↗
Enrolled (actual)
1,095
Serious AEs
0.0%
Results posted
Oct 2025
Primary outcomePrimary: School Attendance — 6.57; 7.34 Mean # days missed
Summary
The study has three aims and involves a clustered randomized controlled trial (RCT) where K-5 schools will be the unit of randomization. Aim 1 involves a qualitative assessment of rural Latino community's social, ethical, behavioral needs and resources for students to return to school and maintain onsite learning. Aim 2 includes a clustered RCT in schools. Aim 3 involves qualitative assessment of implementation outcomes of the Yakima School District (YSD) testing program and risk communication intervention with school stakeholders, parents, and children.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY School Attendance |
6.57; 7.34 | — |
| SECONDARY Emotional Regulation of Index Children at Baseline (T1) |
45.7; 45.4; 49.2; 48.4; 48.8; 48.1 | — |
| SECONDARY Perceived Stress of Parents at Baseline (T1) |
52.6; 52.2; 51.1; 50.5; 48.4; 48.3 | — |
| SECONDARY Emotional Regulation of Index Children at Post Survey 1 (T2) |
45.9; 45.8; 51.7; 51.7; 50.2; 50.1 | — |
| SECONDARY Perceived Stress of Parents at Post Survey 1 (T2) |
53.1; 52.6; 50.9; 49.2; 48.9; 48.8 | — |
Eligibility Criteria
Inclusion Criteria
- Participant attends or works in a participating school for at least 2 days/week.
- Participant must be willing to comply with all study procedures, including weekly online check-ins and phone interviews.
- Participant should have consistent and reliable Internet access, either by smart phone or computer.
- Participant must be comfortable speaking English or Spanish.
- Participant must be able to provide online informed consent and/or legal guardian assent.
Exclusion Criteria
- Individuals unable to provide informed consent / assent, except in cases where the participant has an available legal authorized representative and/or parent
- Individuals who are incarcerated
- Individuals with conditions that may preclude or limit the participant's ability to comply with study procedures, according to the investigators
- Children who are wards of the state and who have clinically-diagnosed dementia, terminal (<5 years) illness, major psychiatric illness, severe hearing impairment, and inability to move, which will be assessed during the distribution of the study recruitment packets to families.
Data sourced from ClinicalTrials.gov (NCT04859699). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.