Attention Bias Study for Infants of Mothers with Depression
Trial Summary
Do I need to stop my current medications to join the trial?
The trial information does not specify whether you need to stop taking your current medications.
What data supports the effectiveness of the treatment Interaction Task, Passive Viewing Task for infants of mothers with depression?
The research suggests that infants of mothers with depression may have heightened attention to fearful faces, indicating a potential vulnerability to emotional challenges. While the specific treatment of Interaction Task and Passive Viewing Task is not directly evaluated, understanding and addressing attentional biases in infants could be beneficial in mitigating these vulnerabilities.12345
Is the Attention Bias Study for Infants of Mothers with Depression safe?
How does the Attention Bias Study for Infants of Mothers with Depression treatment differ from other treatments for this condition?
This treatment is unique because it focuses on understanding and potentially modifying attention biases in infants of mothers with depression, using tasks like the Interaction Task and Passive Viewing Task. Unlike traditional treatments that might focus on medication or therapy for the mother, this approach targets early cognitive patterns in infants, which could help in identifying and addressing vulnerabilities to depression early on.1391011
What is the purpose of this trial?
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.
Eligibility Criteria
This study is for infants born full-term and normal weight, without health problems. Their mothers are divided into two groups: one with no history of depression (low-risk group) and another who had major depressive disorder (MDD) after giving birth (high-risk group). Mothers must not have substance use disorders or a history of bipolar/psychotic disorders.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Baseline Assessment
Infants complete a computer-based task viewing facial displays of emotion while an eye tracker records their gaze. Mother and infants complete a standardized interaction task assessing infant gaze and psychophysiology.
Follow-up
Participants are monitored for changes in eye gaze, heart rate, and respiratory sinus arrhythmia at 3-, 6-, 9-, and 12-month intervals.
Treatment Details
Interventions
- Interaction Task
- Passive Viewing Task
Find a Clinic Near You
Who Is Running the Clinical Trial?
Binghamton University
Lead Sponsor
National Institute of Mental Health (NIMH)
Collaborator