RECRUITING

Development of Attentional Biases for Affective Cues in Infants of Mothers with Depression

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 study is to examine attentional biases for facial displays of emotion as a mechanism of risk in infants of mothers with postpartum major depression, and the potential role of infant arousal in the development of these attentional biases.

Official Title

Development of Attentional Biases for Affective Cues in Infants of Mothers with Depression

Quick Facts

Study Start:2024-11-14
Study Completion:2029-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06835855

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:6 Months
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * The high-risk group (n = 150) will consist of women with at least one episode of MDD since their baby's birth. To qualify for the low-risk group (n = 75), women cannot have a history of any depressive disorder or any current psychiatric diagnoses. Our goal with this recruitment strategy is to maximize variability in levels of depression observed during infants' first two years of life. The two groups will be matched on demographic factors (e.g., age, race/ethnicity, income). Infants will be required to be singleton children born full-term (\> 37 weeks) and normal weight (\> 2,500 grams) with no birth complications or health problems to avoid medical complications contributing to infants' attention, reactivity, and regulation measures.
  1. * Additional exclusion criteria are diagnoses of alcohol or substance use disorders currently or at any point during pregnancy, or lifetime history of bipolar or psychotic disorders.

Contacts and Locations

Study Contact

Brandon E Gibb, Ph.D.
CONTACT
607-777-2511
bgibb@binghamton.edu

Study Locations (Sites)

Binghamton University
Binghamton, New York, 13902
United States

Collaborators and Investigators

Sponsor: Binghamton University

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 Date2024-11-14
Study Completion Date2029-07

Study Record Updates

Study Start Date2024-11-14
Study Completion Date2029-07

Terms related to this study

Keywords Provided by Researchers

  • postpartum
  • infant
  • attention
  • psychophysiology

Additional Relevant MeSH Terms

  • Depression - Major Depressive Disorder