Public Health Management Corporation
Philadelphia, Pennsylvania, 19102, United States
Location status: Recruiting
NCT Number: NCT07400497
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
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Philadelphia, Pennsylvania, 19102, United States
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Families in the intervention group receive the new enhanced supports and participate in six private virtual learning sessions focused on understanding the special education system, improving communication, and enhancing collaboration as co-parents in the IEP process. Each session lasts 60-90 minutes and will be scheduled weekly according to the participants preferred schedule, including evenings and weekends. A workbook with supporting documents for each session will be sent to each participant prior to the start of the sessions.
Other names: FF-SE
Time frame: From enrollment to the last learning session for intervention group, approximately 2 months after enrollment for the control group.
A validated, parent-report questionnaire on key dimensions of the coparenting relationship.
Time frame: From pretest to two months post-intervention
Parent-reported, 17 item scale (Gibaud-Wallston & Wandersman, 1978) assessing parent self-efficacy in accessing services for their child. Higher scores reflect higher degree of sense of competence.
Contact information is provided by the study sponsor or research team.
Penn State University
Other
Family Foundations for Special Education
Acronym: SS-SE
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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