Clinical Trials Directory

Trials / Completed

CompletedNCT07445867

Effectiveness Evaluation of a Comprehensive School Readiness Summer Program for Young Children At-Risk

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
124 (actual)
Sponsor
Florida International University · Academic / Other
Sex
All
Age
4 Years – 6 Years
Healthy volunteers
Not accepted

Summary

This study is a program evaluation or open-trial study of the effectiveness of Summer Academy, a comprehensive summer early intervention program for young children with early learning and disruptive behavior problems (based on the nationally recognized, evidence-based Children's Summer Treatment Program) living in at-risk community settings. The summer program, which is funded by The Children's Trust, will be held annually from June to August from Summer 2016 - Summer 2019 at an early childhood center located in the Liberty City community of Miami, FL. Our aims are to evaluate how well the program helps to prepare young children for the transition to kindergarten and measure to how well progress is maintained at six-month follow-up.

Detailed description

Research design This study is a program evaluation or open-trial study of the effectiveness of FIU Summer Academy, a comprehensive summer early intervention program for young children with early learning and disruptive behavior problems (based on the nationally recognized, evidence-based Children's Summer Treatment Program) living in at-risk community settings. The summer program, which is funded by The Children's Trust, will be held annually from June to August from Summer 2016 - Summer 2019 at an early childhood center located in the Liberty City community of Miami, FL. Our aims are to evaluate how well the program helps to prepare young children for the transition to kindergarten and measure to how well progress is maintained at six-month follow-up. There will be two phases to this study. The first phase (Phase I) will include a series of focus groups to be held annually with parents, teachers, and community stakeholders to obtain feedback on the program to determine what, if any changes, need to be made to current programming to maximize effectiveness. The second phase (Phase II), will consist of direct program evaluation. Procedures to be used In Phase I, we will recruit parents, teachers, and community stakeholders to participate in a 1 hour focus group to obtain feedback on the program to determine what, if any changes, need to be made to current programming to maximize effectiveness. In Phase II, children and their families will be recruited to participate in the summer program through direct school and community referrals. Several process measures (e.g., attendance, satisfaction ratings) will be used to determine the feasibility of the intervention. Other outcome measures, obtained via multiple reports (i.e., parent, teacher, \& observations), examining children's behavioral functioning, self-regulation skills, parental involvement, and academic achievement will be used to both examine aspects of treatment integrity and the effects of the various components of the intervention.

Conditions

Interventions

TypeNameDescription
BEHAVIORALSummer AcademyAll children received a seven-week comprehensive school readiness program adapted from the STP-PreK program (Graziano \& Hart, 2016; Hart, Maharaj, \& Graziano, 2019) that ran from June to early August over the course of three summers. Summer Academy followed the behavioral, social-emotional, academic, and recreational intervention procedures consistent with STP-PreK, including procedures and structure of staff training and supervision, but differed in programmatic aspects in several key ways that were made to be responsive to community needs. Caregivers were required to attend weekly caregiver groups following a modified School Readiness Parent Program (SRPP; Graziano et al., 2018).

Timeline

Start date
2016-03-16
Primary completion
2020-09-01
Completion
2021-09-01
First posted
2026-03-03
Last updated
2026-03-03

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07445867. Inclusion in this directory is not an endorsement.