Psychopathology Clinical Trial
Official title:
A Randomized Controlled Trial to Improve Biobehavioral Regulation Among High-Adversity Mothers and Young Children
Verified date | March 2024 |
Source | Tulane University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study is a randomized controlled confirmatory efficacy trial of virtual Mom Power (MP), a group-based, relationship-focused multifamily preventive intervention.
Status | Active, not recruiting |
Enrollment | 50 |
Est. completion date | May 30, 2026 |
Est. primary completion date | May 30, 2026 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 3 Years and older |
Eligibility | Inclusion Criteria: - Enrollment status in one of the following services: Supplemental Nutrition Assistance Program (SNAP), Family Independence Temporary Assistance Program (FITAP), Medicaid, Special Supplemental Nutrition Program for Women, Infants, and Children (WIC), or Head Start - Maternal age of at least 18 years - Mother is primary caregiver of child - Mother speaks English - Child age is between 3-5 years - Family resides within 8 parish New Orleans metro area Exclusion Criteria: - Mother is not biological mother - Diagnosis of a heart condition in the mother or the child - Presence of a pacemaker in the mother or the child - Child diagnosis of autism or global developmental delay - Active maternal substance use - Active maternal psychosis |
Country | Name | City | State |
---|---|---|---|
United States | Tulane Child and Family Lab | New Orleans | Louisiana |
Lead Sponsor | Collaborator |
---|---|
Tulane University | National Institute of Mental Health (NIMH) |
United States,
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* Note: There are 13 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline maternal depressive symptoms at post-intervention | Mothers will report on their own depressive symptoms using the Patient Health Questionnaire-9 (PHQ-9) at baseline, post-intervention, and 6 month follow up; change in sum scale from baseline at post-intervention will be assessed. Higher scores reflect more depressive symptoms. | At completion of intervention, approximately 3 months | |
Primary | Change from baseline maternal depressive symptoms at 6 month follow up | Mothers will report on their own depressive symptoms using the Patient Health Questionnaire-9 (PHQ-9) at baseline, post-intervention, and 6 month follow up; change in sum scale from baseline to 6 month follow up will be assessed. Higher scores reflect more depressive symptoms. | 6 months (follow up) | |
Primary | Change from baseline maternal posttraumatic stress symptoms at post-intervention | Mothers will report on their own posttraumatic stress symptoms using the Posttraumatic Checklist for Diagnostic and Statistical Manual Diploma in Social Medicine-5 (PCL-5). Sum scales will be assessed at baseline, post-intervention (3 months), and 6 month follow up; change in sum scale from baseline to 3 month follow up will be assessed. Higher scores reflect more posttraumatic stress symptoms. | At completion of intervention, approximately 3 months | |
Primary | Change from baseline maternal posttraumatic stress symptoms at 6 month follow up | Mothers will report on their own posttraumatic stress symptoms using the Posttraumatic Checklist for Diagnostic and Statistical Manual Diploma in Social Medicine-5 (PCL-5). Sum scales will be assessed at baseline, post-intervention (3 months), and 6 month follow up; change in sum scale from baseline to 6 month follow up will be assessed. Higher scores reflect more posttraumatic stress symptoms. | 6 months (follow up) | |
Primary | Change from baseline child behavior at post-intervention | Mothers will report on child behavior on the Child Behavior Checklist (CBCL 1.5-5). Sum scores will be used. Higher scores reflect more behavior problems. | At completion of intervention, approximately 3 months | |
Primary | Change from baseline child behavior at 6 month follow up. | Mothers will report on child behavior on the Child Behavior Checklist (CBCL 1.5-5). Sum scores will be used. Higher scores reflect more behavior problems. | 6 months (follow up) | |
Secondary | Change in parenting stress from baseline to post-intervention | Mothers will report on their own parenting stress using the Parenting Stress Index - 4, Short Form (PSI-SF); change in the the Total Stress scale from baseline to post-assessment (3 months) will be examined. Higher scores reflect more parenting stress. | At completion of intervention, approximately 3 months | |
Secondary | Change in parenting stress from baseline to 6 month follow up | Mothers will report on their own parenting stress using the Parenting Stress Index - 4, Short Form (PSI-SF); change in the the Total Stress scale from baseline to follow up (6 months) will be examined. Higher scores reflect more parenting stress. | 6 months | |
Secondary | Change in self-report parent child relationship from baseline to post intervention | Mothers will report on their own parenting stress using the Parenting Stress Index - 4, Short Form (PSI-SF); change in the the Parent Child Dysfunctional Interaction scale from baseline to post-assessment (3 months) will be examined. Higher scores reflect more dysfunction. | At completion of intervention, approximately 3 months | |
Secondary | Change in self-report parent child relationship from baseline to follow up | Mothers will report on their own parenting stress using the Parenting Stress Index - 4, Short Form (PSI-SF); change in the the Parent Child Dysfunctional Interaction scale from baseline to follow up (6 months) will be examined. Higher scores reflect more dysfunction. | 6 months | |
Secondary | Change in maternal social support from baseline to post intervention | Mothers will report on their perceived social support a using the Multidimensional Scale of Perceived Social Support (MSPSS). Change from baseline to post intervention (3 months) will be examined. Higher scores reflect more social support. | At completion of intervention, approximately 3 months | |
Secondary | Change in maternal social support from baseline to follow up | Mothers will report on their perceived social support a using the Multidimensional Scale of Perceived Social Support (MSPSS). Change from baseline to follow up (6 months) will be examined. Higher scores reflect more social support. | 6 months | |
Secondary | Change in observed parenting sensitivity from baseline to post-intervention | Parenting sensitivity will be assessed at baseline and post intervention (3 months) with an observational measure. Video tapes of parent-child interactions during a 5-minute period of free play and a 5-minute period of structured interaction with a challenging puzzle will be coded using the Coding Interactive Behavior (CIB) measure. Parenting sensitivity scales will be used. Higher scores reflect more sensitivity. | At completion of intervention, approximately 3 months | |
Secondary | Change in Working Models from baseline to post-intervention | Mothers and evaluators will complete a Working Model of the Child Interview (WMCI) at baseline and post-intervention (3 months) to assess parents' internal working model classifications. Classifications as Balanced, Disengaged, and Distorted will be used. Classification as balance is considered a more adaptive outcome. | At completion of intervention, approximately 3 months | |
Secondary | Change in maternal emotion regulation from baseline to post-intervention | Mothers will report on their difficulties in emotion regulation (Difficulties in Emotion Regulation Scale). Change in the sum score from baseline to post-intervention will be examined. Higher scores reflect more difficulties in emotion regulation. | At completion of intervention, approximately 3 months | |
Secondary | Change in maternal emotion regulation from baseline to follow up | Mothers will report on their difficulties in emotion regulation (Difficulties in Emotion Regulation Scale). Change in the sum score from baseline to 6 month follow up will be examined. Higher scores reflect more difficulties in emotion regulation. | 6 months | |
Secondary | Change in maternal emotion regulation while parenting from baseline to post intervention | Mothers will report on their parenting-specific behavioral self-regulation (Regulating Emotions in Parenthood). Change in the sum score from baseline to post intervention will be examined. | At completion of intervention, approximately 3 months | |
Secondary | Change in maternal emotion regulation while parenting from baseline to follow up | Mothers will report on their parenting-specific behavioral self-regulation (Regulating Emotions in Parenthood). Change in the sum score from baseline to 6 month follow up will be examined. | 6 months | |
Secondary | Change in maternal resting Respiratory Sinus Arrhythmia from baseline to post-intervention | At baseline assessments and at post-intervention assessments, electrocardiogram data will be collected during a 2 minute neutral video tsak. ECG signals will be synchronized at acquisition with video and processed offline using Mindware software; research assistants will visually inspect for missing or erroneously identified R-peaks. Using spectral analysis of interbeat intervals, high-frequency heart rate variability will be extracted to quantify respiratory sinus arrhythmia (RSA) within frequency bandwidths associated with respiration (.15-.40 for mothers) and log-transformed. Change in resting RSA from baseline to post-intervention will be examined. Higher resting RSA is expected post-intervention. | At completion of intervention, approximately 3 months | |
Secondary | Change in maternal Respiratory Sinus Arrhythmia reactivity from baseline to post-intervention | Electrocardiogram data will be collected during a 2 minute baseline neutral video task and a 5 minute parent-child puzzle teaching task. ECG signals will be synchronized at acquisition with video and processed offline using Mindware software; research assistants will visually inspect for missing or erroneously identified R-peaks. Using spectral analysis of interbeat intervals, high-frequency heart rate variability will be extracted to quantify RSA within frequency bandwidths associated with respiration (24-1.04 for children) and log-transformed. Respiratory Sinus Arrhythmia reactivity in response to the puzzle task will be assessed at baseline and post-intervention (3 months) | At completion of intervention, approximately 3 months | |
Secondary | Change in child resting Respiratory Sinus Arrhythmia from baseline to post-intervention | Electrocardiogram data will be collected during a 2 minute baseline neutral video task. ECG signals will be synchronized at acquisition with video and processed offline using Mindware software; research assistants will visually inspect for missing or erroneously identified R-peaks. Using spectral analysis of interbeat intervals, high-frequency heart rate variability will be extracted to quantify RSA within frequency bandwidths associated with respiration (24-1.04 for children) and log-transformed. Change in children's resting Respiratory Sinus Arrhythmia during the neutral task will be assessed from baseline to post-intervention (3 months). Higher resting RSA is expected post-intervention. | At completion of intervention, approximately 3 months | |
Secondary | Change in child Respiratory Sinus Arrhythmia reactivity from baseline to post-intervention | Electrocardiogram data will be collected during a 2 minute baseline neutral video task and a 5 minute parent-child puzzle teaching task. ECG signals will be synchronized at acquisition with video and processed offline using Mindware software; research assistants will visually inspect for missing or erroneously identified R-peaks. Using spectral analysis of interbeat intervals, high-frequency heart rate variability will be extracted to quantify RSA within frequency bandwidths associated with respiration (24-1.04 for children) and log-transformed. Change in children's Respiratory Sinus Arrhythmia reactivity during the puzzle task from baseline to post-intervention will be assessed. | At completion of intervention, approximately 3 months |
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