Hybrid Delivery to Increase Access and Sustainability: Evaluating ezParent Implementation
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorKlein Buendel, Inc.
About this trial
The goal of this study is to evaluate the effects of the hybrid ezParent program (e.g., web-based training program plus synchronous group sessions) on parent and child outcomes in a community setting serving parents of children 2-5 years old. Parent participants will complete surveys at baseline, and 10 and 24-weeks post baseline.
Eligibility criteria
Qualifiers
Parent or legal guardian of a 2-5-year-old child receiving services at the partnering organization site.
Speaks English or Spanish.
Has a smartphone, tablet, or computer with Wi-Fi access to receive the ezParent program.
Disqualifiers
None
Trial design
Treatments tested in this trial
- ezParent
Treatment groups
516 Participants
are divided into 2 treatment groupsSponsors and collaborators
Klein Buendel, Inc.
Lead sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborator
Ohio State University
Collaborator
Johns Hopkins University
Collaborator
Source ClinicalTrials.gov