RECRUITING

Childhood Activities Nutrition and Development Oversight

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 overall goal of this study is to understand how common conditions in childhood develop and if by providing specific health education and resources to parents/caregivers we can promote healthy development. This study will provide information and instruction on several aspects of infant care including, sleep, nutrition, building a healthy relationship with your baby, and healthy screen time use.

Official Title

Childhood Activities Nutrition and Development Oversight

Quick Facts

Study Start:2022-03-03
Study Completion:2027-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05258656

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:Not specified to 26 Weeks
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * Parent/guardian(s) must understand and provide informed consent
  2. * Infant \<26 weeks of age at enrollment
  3. * Willing to be randomized to either intervention or control
  4. * In good general health as evidenced by medical history
  5. * Stated willingness to comply with all study procedures and availability for the duration of the study
  6. * Child assigned male or female sex at birth
  1. * Infant completed less than 28 weeks gestation
  2. * Co-morbid medical diagnoses that would prevent caregivers from initiating solid foods per protocol, such as dysphagia, chronic aspiration, malformations, etc.
  3. * Co-morbid medical diagnoses that would require specialized diet/nutritional needs, such as congenital heart disease, genetic/metabolic disorders, malignancy, etc.
  4. * Caregivers who express unwillingness to introduce peanut, milk, egg, or cashew
  5. * Caregivers who cannot provide informed consent in English or Spanish
  6. * Parents planning to move away from study sites before child is 12 months of age
  7. * Investigator or designee considers that the participant or parent/guardian would be unsuitable for inclusion in the study
  8. * Infant with a sibling enrolled in the study

Contacts and Locations

Study Contact

Neeha Shrestha, MPH
CONTACT
312-503-4687
neeha.shrestha@northwestern.edu

Principal Investigator

Ruchi S Gupta, MD MPH
PRINCIPAL_INVESTIGATOR
Northwestern University Feinberg School of Medicine

Study Locations (Sites)

Ann & Robert H Lurie Children's Hospital of Chicago
Chicago, Illinois, 60611
United States
Rush University Medical Center
Chicago, Illinois, 60612
United States

Collaborators and Investigators

Sponsor: Northwestern University

  • Ruchi S Gupta, MD MPH, PRINCIPAL_INVESTIGATOR, Northwestern University Feinberg School 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 Date2022-03-03
Study Completion Date2027-12-31

Study Record Updates

Study Start Date2022-03-03
Study Completion Date2027-12-31

Terms related to this study

Keywords Provided by Researchers

  • infant development
  • health promotion

Additional Relevant MeSH Terms

  • Environmental Exposure