RECRUITING

Partners in Children's Health (CSN): a Randomized Trial of an Attachment Based Intervention

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 goal of this randomized controlled trial is to evaluate the impacts of an attachment-based intervention (Attachment Biobehavioral Catch-Up (ABC) and Home Book-of-the-Week (HBOW) program on emerging health outcomes (i.e., common childhood illnesses, body mass index, and sleep) in low-income Latino children (N=260; 9 months at enrollment). It is hypothesized that children randomized to ABC will have better health outcomes in comparison to the HBOW control group.

Official Title

Effects of Attachment-Based Intervention on Low-Income Latino Children's Emerging Health Outcomes

Quick Facts

Study Start:2023-10-09
Study Completion:2028-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06002685

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:8 Months to 12 Months
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * Biological mothers
  2. * Identify as Latina
  3. * Speak English or Spanish
  4. * Primiparous and multiparous
  5. * Have a 9-month-old child enrolled in Medicaid
  1. * Children born prematurely (gestational age \< 37 weeks)
  2. * Children who have major complex medical conditions (e.g., heart or autoimmune conditions) that could interfere with participation in intervention sessions and/or research assessments.

Contacts and Locations

Study Contact

Lisa Berlin, PhD
CONTACT
410.706.6392
lberlin@ssw.umaryland.edu
Roderick Rose, PhD
CONTACT
410.706.7023
rrose@ssw.umaryland.edu

Principal Investigator

Lisa Berlin, PhD
PRINCIPAL_INVESTIGATOR
University of Maryland
Natalie Slopen, PhD
STUDY_CHAIR
Harvard School of Public Health (HSPH)
Cathi Propper, PhD
STUDY_CHAIR
Department of Psychology and Neuroscience at UNC Chapel Hill

Study Locations (Sites)

University of Maryland
Baltimore, Maryland, 21201
United States

Collaborators and Investigators

Sponsor: University of Maryland, Baltimore

  • Lisa Berlin, PhD, PRINCIPAL_INVESTIGATOR, University of Maryland
  • Natalie Slopen, PhD, STUDY_CHAIR, Harvard School of Public Health (HSPH)
  • Cathi Propper, PhD, STUDY_CHAIR, Department of Psychology and Neuroscience at UNC Chapel Hill

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 Date2023-10-09
Study Completion Date2028-01

Study Record Updates

Study Start Date2023-10-09
Study Completion Date2028-01

Terms related to this study

Additional Relevant MeSH Terms

  • Respiratory Disease
  • Inflammation
  • Insufficient Sleep
  • Digestive Disease
  • Skin Conditions
  • Body Mass Index
  • Infections
  • Allergies
  • Congestion
  • Antibiotic Use
  • Overweight and Obesity