Hybrid Delivery to Increase Access and Sustainability: Evaluating ezParent Implementation

Recruiting N/A Interventional Study
Parenting Prevention Program Implementation Early Childhood
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
516 (estimated)
Sponsor
Klein Buendel, Inc. · Industry
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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.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 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. Exclusion Criteria: • Parents who have previously …
Contacts

Susan M Breitenstein, PhD

614-688-4614

breitenstein.5@osu.edu

CONTACT