Neurodevelopmental Outcomes in Children: Strengthening the Caregiver-Child Story
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorBaylor College of Medicine
About this trial
The main goal of this research is to help families who are experiencing food insecurity (FI) and help mothers with depression.
The next goal is to provide other resources to help with household needs like rent or utility assistance, health insurance, anxiety, and depression. Our theory is that helping with food insecurity, household needs, and emotional health will help children and families.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Caregivers of young children (0-36 months of age) hospitalized at Texas Children's Hospital on acute care units.
English or Spanish speaking caregiver.
Age of caregiver ≥ 18 years old.
Hospital day 2 or later of patient admission.
Disqualifiers
Caregivers who do not have primary custody
Children in Child Protective Services (CPS) custody
Caregivers who live outside of Texas (due to lack of Houston Food Bank resources outside of Texas)
Previous enrollment in this study (H-53133) or H-57296.
Trial population
The population are the caregivers of children hospitalized at Texas Children's Hospital.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
2,000 Participants
are grouped into 2 trial groupsGroup A: Neurocognitive Outcomes
Group B: Neurodevelopmental Outcomes
Trial outcomes
Primary outcomes
1
Maternal Child Bonding
The validated Maternal Attachment Inventory will be used for data collection. Higher scores indicate greater maternal child bonding.
Time frame
3 monthsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Baylor College of Medicine
Lead sponsor
Episcopal Health Foundation
Collaborator
Source ClinicalTrials.gov