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Family Foundations for Special Education Trial

Study acronym: SS-SE
StatusCompleted
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Trial completed Primary completion date changed from estimate of Mar 31, 2026 to May 31, 2026 · Enrollment target: estimated 120 to confirmed 110 · Study completion date changed from estimate of Dec 30, 2026 to Jul 1, 2026 · 2 more Show 5 more changesShow less
    • Primary completion date changed from estimate of Mar 31, 2026 to May 31, 2026
    • Enrollment target: estimated 120 to confirmed 110
    • Study completion date changed from estimate of Dec 30, 2026 to Jul 1, 2026
    • Eligibility criteria expanded, about 6 words
    • Site details revised
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this clinical trial is to assess the program's impact on parent self-efficacy and co-parental support around (a) accessing health and educational services and (b) parenting for co-parents of children with disabilities entering the Special Education system before their first Individualized Education Program (IEP) meeting. The main questions it aims to answer are: Does the program improve co-parenting support and coordination and parent efficacy in accessing services for and parenting their child? Does the program improve parent mental health, service access, engagement, and adherence? Does the program improve parenting quality? Does the program improve child adjustment (mental and behavioral health, academic engagement)? Researchers will compare pretest and posttest questionnaires from Treatment Group A with Control Group B to see if the program improves parent and child well-being, co-parenting relations, relations with service providers, ability to access services and meaningfully participate in IEP and other meetings. Participants will: * Complete pre- and post-test questionnaires * Treatment Group A will participate in 6 learning sessions, each 1 hour to 1½ hour long, over a 6-8 week period
Trial Details
NCT Number NCT07400497
Lead Sponsor Penn State University
Collaborators: Public Health Management Corporation, William Penn Foundation
Conditions Mental Health
Enrollment 110 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov