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Head Start REACH: Strengthening Outreach, Recruitment and Engagement Approaches With Families

NCT05145933 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 174

Last updated 2021-12-06

No results posted yet for this study

Summary

Mathematica, funded by the Administration for Children and Families (ACF) Office of Planning, Research, and Evaluation (OPRE) in the U.S. Department of Health and Human Services (HHS) will collect descriptive information for the Head Start REACH: Strengthening Outreach, Recruitment and Engagement Approaches with Families (Head Start REACH) study. The investigators will conduct qualitative case studies in six sites. The goal of these case studies in the Head Start REACH study is to provide an in-depth understanding of (1) the approaches that are likely to be successful for the recruitment, selection, enrollment, and retention (RSER) of families who are experiencing adversities; (2) the factors that affect the implementation of these approaches and; (3) the experiences of such families, both enrolled and non-enrolled in Head Start.

Data collection will occur in spring 2022. The investigators will conduct qualitative, semi-structured interviews with staff across the six sites who are involved in RSER efforts and provide services to families experiencing adversities, including those in Head Start programs and in the community organizations with which the programs partner. The investigators will also conduct focus groups with families who are being served by Head Start programs and/or the community partner organizations.

Conditions

  • Early Intervention, Educational (Head Start and Early Head Start Access and Participation)

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-01-03
Primary Completion
2022-08-31
Completion
2023-06-30

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05145933 on ClinicalTrials.gov