ACTIVE_NOT_RECRUITING

Neurodevelopmental Outcomes in Children: Strengthening the Caregiver-Child Story

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Neurodevelopmental Outcomes in Children: Strengthening the Caregiver-Child Story

Quick Facts

Study Start:2023-06-14
Study Completion:2026-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05809115

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Caregivers of young children (0-36 months of age) hospitalized at Texas Children's Hospital on acute care units.
  2. * English or Spanish speaking caregiver.
  3. * Age of caregiver ≥ 18 years old.
  4. * Hospital day 2 or later of patient admission.
  1. * Caregivers who do not have primary custody
  2. * Children in CPS custody
  3. * Caregivers who live outside of Texas (due to lack of Houston Food Bank resources outside of Texas)
  4. * Previous enrollment in this study.
  5. * Patient is in the process of being discharged/observation status administration.
  6. * Caregiver is not the primary caregiver.

Contacts and Locations

Principal Investigator

Michelle Lopez, MD, MPH
PRINCIPAL_INVESTIGATOR
Baylor College of Medicine

Study Locations (Sites)

Texas Children's Hospital
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: Baylor College of Medicine

  • Michelle Lopez, MD, MPH, PRINCIPAL_INVESTIGATOR, Baylor College of Medicine

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-06-14
Study Completion Date2026-03

Study Record Updates

Study Start Date2023-06-14
Study Completion Date2026-03

Terms related to this study

Additional Relevant MeSH Terms

  • Food Insecurity
  • Depression
  • Anxiety