Protocol Section
The Protocol Section is one of the main sections in ClinicalTrials.gov data structure. It contains protocol-related information for clinical trials, including identification, status, design, eligibility, and other key details about how the trial is structured and conducted.
Protocol Section path is as follows:
Study -> Protocol Section -> Protocol Modules (Identification, Status, Design, Eligibility, etc.)
Protocol Section
Ignite Creation Date:
2025-12-25 @ 2:17 AM
Ignite Modification Date:
2025-12-25 @ 2:17 AM
NCT ID:
NCT04294134
Description:
For all study participants, study staff are required to share the following data elements for each study participant with the Children's Bureau, Mathematica Policy Research Institute, and Walter R. McDonald \& Associates (WMRA): 1) administrative data regarding safety and permanency records for the child (from birth to present day) for children who are a part of a study case; 2) substance use treatment records for adults (from age 18 to present day) who are a part of a study case from one year prior to study enrollment to one year following study exit; 3) all participant responses to study questionnaires; and 4) dates of enrollment, service logs and dates of service from each of the participant's encounters with a Child-Parent Specialist, and case closure; 5) child's date of birth. Data will be reported using the Department of Health and Human Services' secure web-based platform, RPG-EDS.
Study:
NCT04294134
Study Brief:
MIO-CPP to Improve the Well-being, Permanency, and Safety Outcomes for Young Children at Risk of or in Out-of-home Placement in Philadelphia and Bucks Counties, and Affected by Maternal Substance Use