- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05477901
Impacts of Cash Transfers on Child Neurodevelopment (Auxilio Brasil)
Mental Health and Bolsa Familia: A Mechanistically Focused Clinical Trial of a Cash Transfer Intervention on Child Brain, Behavior, and Mental Health
This study examines the impact of Auxilio Brasil (AB), a cash transfer program to mothers of school-age children, on resource-deprived populations in Brazil and its protective effects on child neurodevelopment and mental health. The investigators will conduct a randomized clinical trial (RCT) among those already receiving AB in which 300 families will be randomized in a 1:1 ratio to receive either a high ($40/month) or low ($2/month) supplemental transfer for 2 years. Three hundred children (index child participants; 7-10 years old) will be enrolled across both study arms. Additionally, up to 150 siblings ("sibling participants;" 7-10 years old) will be enrolled. Eligible families who decide to participate will sign a study-specific informed consent (mother) and assent (child) form. The UNIFESP team will conduct the respective assessments at baseline, approximately 8- and 16- months, 24-months and approximately 6-months post-RCT.
Aim 1: Determine the impact of high vs low cash transfers on children's exposure to adversities (ACEs) and neurodevelopment.
Aim 2: Determine the impact of cash transfers on children's inflammatory markers and HPA activity/cortisol.
Exploratory Aim: The investigators will explore (i) whether sex/gender of the children moderates the pathways in the above mediation model; and (ii) whether cash transfer-related effects persist 6 months post-RCT.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Numerous studies link childhood poverty with altered neurodevelopment with the most robust effects often in brain substrates related to executive functions (EF). Poverty is associated with reduced grey matter thickness and surface area of the prefrontal cortex (PFC), a key structure underlying EF (4,5) Poverty is also associated with altered structure and function of the hippocampus - a region essential for memory and cognitive control (5,6). Effects of poverty on brain development are thought to give rise to the well described associations between poverty, impairments in EF, and risk for mental illness (18). The possibility of lifting children out of poverty and thereby tempering poverty's malignant neurodevelopmental effects remains largely untested, particularly with brain and behavioral measures and within LMICs where poverty is widespread. To address this gap, the investigators propose a randomized clinical trial (RCT) to be conducted in low-income families in Sao Paulo, Brazil that will examine causal effects of a cash transfer program on neurodevelopment in youth. Our study builds off an existing cash transfer program (CTP) - Auxilio Brasil (AB) - and augments the cash transfer amount to a level sufficient to lift a family out of extreme poverty and poverty. Our RCT design will allow for novel causal inferences linking cash transfers to brain/behavior outcomes, while testing mechanistic hypotheses. Because the investigators are building off AB, a well-established program with a successful, national infrastructure for transferring cash, our findings could rapidly move toward implementation. Our study will inform critical unanswered questions about pasting, and CTPs generally, that could support their broader and more targeted implementation - First, if augmenting AB removes a family from poverty, does this protect child neurodevelopment? And second, if this augmented AB program protects neurodevelopment, what are the mechanisms that explain this? Providing this mechanistic framework is a key step toward refining AB and other CTPs, facilitating for example, studies aimed at targeting populations most likely to benefit, optimizing the dose/amount of the transfers, and determining the ideal timing/duration of CTPs.
Aims and Hypotheses
Aim 1: Determine the impact of high vs low cash transfers on children's exposure to adversities (ACEs) and neurodevelopment. Eligible families will be those already enrolled in Brazil's national AB program. Relative to low cash transfers, children of mothers who received high cash transfers will have:
Hypothesis 1A (H1A) - [ACEs] fewer new onset ACEs over the 24-month course of the RCT; H1B - [Neurodevelopment] greater pre-vs-post RCT increases in prefrontal activation during an EF fMRI task (Simon task),10 increased connectivity within EF-related PFC/mesolimbic circuits (resting fMRI and diffusion MRI), and improvements in EF behaviors.
Aim 2: Determine the impact of cash transfers on children's inflammatory markers and HPA activity/cortisol.
Hypothesis 2A (H2A) - Relative to low cash transfers, children of mothers who received high cash transfers will have lower pre vs-post RCT levels of pro-inflammatory markers (e.g., CRP, Il-6, TNF-a; from blood draws) and hair cortisol (HPA activity over past 2-3 months).
Hypothesis 2B (H2B) - Inflammatory and HPA activity levels (H2A) will be lower in children with fewer new onset ACEs (i.e., new ACEs occurring during the 24-month RCT). H2C [Mediation] - The effects of high cash transfers on neurodevelopment (H1B) will be mediated by the impact of cash transfers on reducing new onset ACEs (H1A) and lower inflammation and HPA activity (H2A & H2B), while taking into account covariates and three additional pathways (see A.9 And C.6.3).
Exploratory Aim: The investigators will explore (i) whether sex/gender of the children moderates the pathways in the above mediation model (H2C); and (ii) whether cash transfer-related effects - reducing new onset ACEs and symptoms (CBCL), and improved EF behavior - persist 6 months post-RCT.
Impact: Designed to decrease inequalities, AB is one of the largest social interventions in the world, yet its impact on child mental health is unknown. Our strategy, rather than relying on prohibitively expensive multi-site designs, proposes to generate evidence about the impact of AB on child neurodevelopmental outcomes by focusing on specific, well-supported mechanisms that may underlie mental illness risk. Our findings will have strong implications for tailoring the impact of cash transfer policies to maximize child mental health gains.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Cristiane Duarte, PhD
- Phone Number: 646-774-5801
- Email: cristiane.duarte@nyspi.columbia.edu
Study Locations
-
-
São Paulo
-
São Paulo, São Paulo, Brazil, 04023
- Recruiting
- UNIFESP
-
Contact:
- Andrea Jackowski, PhD
- Phone Number: +55-11985855785
- Email: andrea.jackowski@gmail.com
-
-
-
-
New York
-
New York, New York, United States, 10032
- Not yet recruiting
- New York State Psychiatric Institute
-
Contact:
- Cristiane Duarte, PhD
- Phone Number: (646)774-5801
- Email: Cristiane.Duarte@nyspi.columbia.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Mother:
Inclusion Criteria:
- Age 23-45 years old
- Receiving AB cash transfers
- Has at least two or more children ages 7- 10 years old at time of recruitment (up to 4 children per family)
- Able to consent
Exclusion Criteria:
1. Mother and child do not reside in same household
Child:
Inclusion Criterion
- Age 7-10 years old
- Intellectual Disability
Exclusion Criterion
- Does not reside in same household as the mother
- Major Axis I disorder (e.g., Autism, Schizophrenia, Bipolar)
- Severe Disability
- MRI contradictions (index child only)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
High supplemental transfer: $40 a month
|
Supplemental cash transfer ($40/month)
|
|
No Intervention: Control
Low supplemental transfer: $2 a month
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Adverse Childhood Experiences (ACEs) - FHE
Time Frame: Baseline
|
Family History Epidemiologic screener is a 9-item (+subitems) checklist to asses child's ACEs, more checked items mean more ACEs.
|
Baseline
|
|
Changes in Adverse Childhood Experiences (ACEs) - FHE
Time Frame: 8 months
|
Family History Epidemiologic screener is a 9-item (+subitems) checklist to asses child's ACEs, more checked items mean more ACEs.
|
8 months
|
|
Changes in Adverse Childhood Experiences (ACEs) - FHE
Time Frame: 16 months
|
Family History Epidemiologic screener is a 9-item (+subitems) checklist to asses child's ACEs, more checked items mean more ACEs.
|
16 months
|
|
Changes in Adverse Childhood Experiences (ACEs) - FHE
Time Frame: 24 months
|
Family History Epidemiologic screener is a 9-item (+subitems) checklist to asses child's ACEs, more checked items mean more ACEs.
|
24 months
|
|
Changes in Adverse Childhood Experiences (ACEs) - FHE
Time Frame: 6 months post-RCT
|
Family History Epidemiologic screener is a 9-item (+subitems) checklist to asses child's ACEs, more checked items mean more ACEs.
|
6 months post-RCT
|
|
Adverse Childhood Experiences (ACEs) - CTC
Time Frame: Baseline
|
Brazilian version of the Parent-Child Conflict Tactics Scale: 22-item checklist with following subscales: non-violent discipline (NVD), psychological aggression (PSY), corporal punishment (CP), and physical maltreatment (PM).
More checks in each subscales means behavior is performed more often.
|
Baseline
|
|
Changes in Adverse Childhood Experiences (ACEs) - CTC
Time Frame: 8 months
|
Brazilian version of the Parent-Child Conflict Tactics Scale: 22-item checklist with following subscales: non-violent discipline (NVD), psychological aggression (PSY), corporal punishment (CP), and physical maltreatment (PM).
More checks in each subscales means behavior is performed more often.
|
8 months
|
|
Changes in Adverse Childhood Experiences (ACEs) - CTC
Time Frame: 16 months
|
Brazilian version of the Parent-Child Conflict Tactics Scale: 22-item checklist with following subscales: non-violent discipline (NVD), psychological aggression (PSY), corporal punishment (CP), and physical maltreatment (PM).
More checks in each subscales means behavior is performed more often.
|
16 months
|
|
Changes in Adverse Childhood Experiences (ACEs) - CTC
Time Frame: 24 months
|
Brazilian version of the Parent-Child Conflict Tactics Scale: 22-item checklist with following subscales: non-violent discipline (NVD), psychological aggression (PSY), corporal punishment (CP), and physical maltreatment (PM).
More checks in each subscales means behavior is performed more often.
|
24 months
|
|
Changes in Adverse Childhood Experiences (ACEs) - CTC
Time Frame: 6 months-post RCT
|
Brazilian version of the Parent-Child Conflict Tactics Scale: 22-item checklist with following subscales: non-violent discipline (NVD), psychological aggression (PSY), corporal punishment (CP), and physical maltreatment (PM).
More checks in each subscales means behavior is performed more often.
|
6 months-post RCT
|
|
Child internalizing and externalizing symptoms
Time Frame: Baseline
|
Maternal report of The Child Behavior Checklist, internalizing (score ranges from 0 to 33) and externalizing (score ranges from 0 to 35) scales.
More checks in each scale means more internalizing or externalizing symptoms.
|
Baseline
|
|
Changes in Child internalizing and externalizing symptoms
Time Frame: 8 months
|
Maternal report of The Child Behavior Checklist, internalizing (score ranges from 0 to 33) and externalizing (score ranges from 0 to 35) scales.
More checks in each scale mean more internalizing or externalizing symptoms.
|
8 months
|
|
Changes in Child internalizing and externalizing symptoms
Time Frame: 16 months
|
Maternal report of The Child Behavior Checklist, internalizing (score ranges from 0 to 33) and externalizing (score ranges from 0 to 35) scales.
More checks in each scale mean more internalizing or externalizing symptoms.
|
16 months
|
|
Changes in Child internalizing and externalizing symptoms
Time Frame: 24 months
|
Maternal report of The Child Behavior Checklist, internalizing (score ranges from 0 to 33) and externalizing (score ranges from 0 to 35) scales.
More checks in each scale mean more internalizing or externalizing symptoms.
|
24 months
|
|
Changes in Child internalizing and externalizing symptoms
Time Frame: 6 months-post RCT
|
Maternal report of The Child Behavior Checklist, internalizing (score ranges from 0 to 33) and externalizing (score ranges from 0 to 35) scales.
More checks in each scale mean more internalizing or externalizing symptoms.
|
6 months-post RCT
|
|
Access to health care
Time Frame: Baseline
|
The assessment will be based on maternal report about each child's health care utilization history including primary care, urgent care, and hospital care.
Primary care visits will be classified by purpose: vaccination, routine check-up, or sick visits.
Similar procedures to the ones in place in our ongoing study will be used to obtain child medical records in the primary care unit.
|
Baseline
|
|
Changes in Access to health care
Time Frame: 8 months
|
The assessment will be based on maternal report about each child's health care utilization history including primary care, urgent care, and hospital care.
Primary care visits will be classified by purpose: vaccination, routine check-up, or sick visits.
Similar procedures to the ones in place in our ongoing study will be used to obtain child medical records in the primary care unit.
|
8 months
|
|
Changes in Access to health care
Time Frame: 16 months
|
The assessment will be based on maternal report about each child's health care utilization history including primary care, urgent care, and hospital care.
Primary care visits will be classified by purpose: vaccination, routine check-up, or sick visits.
Similar procedures to the ones in place in our ongoing study will be used to obtain child medical records in the primary care unit.
|
16 months
|
|
Changes in Access to health care
Time Frame: 24 months
|
The assessment will be based on maternal report about each child's health care utilization history including primary care, urgent care, and hospital care.
Primary care visits will be classified by purpose: vaccination, routine check-up, or sick visits.
Similar procedures to the ones in place in our ongoing study will be used to obtain child medical records in the primary care unit.
|
24 months
|
|
Child brain MRI scan
Time Frame: Baseline
|
Child participants will undergo an MRI scan (~1 hour) to examine the function and connectivity of EF-related brain systems
|
Baseline
|
|
Changes in Child brain MRI scan
Time Frame: 24 months
|
Child participants will undergo an MRI scan (~1 hour) to examine the function and connectivity of EF-related brain systems
|
24 months
|
|
Child Executive Function
Time Frame: Baseline
|
Brazilian version of the Child Executive Functions Battery (CEF-B) assesses working memory, inhibition, flexibility and planning.
Score ranges vary by domain.
Higher scores mean higher capacity on specific domain.
|
Baseline
|
|
Changes in Child Executive Function
Time Frame: 24 months
|
Brazilian version of the Child Executive Functions Battery (CEF-B) assesses working memory, inhibition, flexibility and planning.
Score ranges vary by domain.
Higher scores mean higher capacity on specific domain.
|
24 months
|
|
Changes in Child Executive Function
Time Frame: 6 months-post RCT
|
Brazilian version of the Child Executive Functions Battery (CEF-B) assesses working memory, inhibition, flexibility and planning.
Score ranges vary by domain.
Higher scores mean higher capacity on specific domain.
|
6 months-post RCT
|
|
Biospecimen - Child hair sample
Time Frame: Baseline
|
Child hair samples to measure HPA activity (cortisol)
|
Baseline
|
|
Biospecimen - Changes in Child hair sample
Time Frame: 24 months
|
Child hair samples to measure HPA activity(cortisol)
|
24 months
|
|
Biospecimen - Blood Draw - IL-6
Time Frame: Baseline
|
Primary immune measures will consist of IL-6 and CRP, consistent with prior research on inflammation and neurodevelopment.
|
Baseline
|
|
Biospecimen - Blood Draw - Change in IL-6
Time Frame: 24 months
|
Primary immune measures will consist of IL-6 and CRP, consistent with prior research on inflammation and neurodevelopment.
|
24 months
|
|
Biospecimen - Blood Draw - CRP
Time Frame: Baseline
|
Primary immune measures will consist of IL-6 and CRP, consistent with prior research on inflammation and neurodevelopment.
|
Baseline
|
|
Biospecimen - Blood Draw - Change in CRP
Time Frame: 24 months
|
Primary immune measures will consist of IL-6 and CRP, consistent with prior research on inflammation and neurodevelopment.
|
24 months
|
|
Family Adaptability and Cohesion Evaluation Scale-III (FACES-III)
Time Frame: Baseline
|
This 20-item parent-report scale assesses family cohesion and adaptability.
Cohesion: scores range from 0-50, higher scores mean a more cohesive family.
Adaptability: scores range from 0-50, higher scores mean a more adaptable family.
|
Baseline
|
|
Change in Family Adaptability and Cohesion Evaluation Scale-III (FACES-III)
Time Frame: 24 months
|
This 20-item parent-report scale assesses family cohesion and adaptability.
Cohesion: scores range from 0-50, higher scores mean a more cohesive family.
Adaptability: scores range from 0-50, higher scores mean a more adaptable family.
|
24 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Food insecurity
Time Frame: Baseline, 24 months
|
Mothers will be interviewed using the Brazilian adaptation of the Household Food insecurity.
Scores range from 0-8.
Higher scores mean more food insecurity.
|
Baseline, 24 months
|
|
Changes in Food insecurity
Time Frame: 24 months
|
Mothers will be interviewed using the Brazilian adaptation of the Household Food insecurity.
Scores range from 0-8.
Higher scores mean more food insecurity.
|
24 months
|
|
Home observation/environment
Time Frame: Baseline
|
The quality of the child's home environment will be assessed with the Home Observation Measurement of the Environment (HOME) Inventory.
Scores range from 0 to 55. Higher scores mean more quality and quantity of stimulation and support available to child in the home.
|
Baseline
|
|
Changes in Home observation/environment
Time Frame: 24 months
|
The quality of the child's home environment will be assessed with the Home Observation Measurement of the Environment (HOME) Inventory.
Scores range from 0 to 55. Higher scores mean more quality and quantity of stimulation and support available to child in the home.
|
24 months
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Cristiane Duarte, PhD, New York State Psychiatric Institute
- Principal Investigator: Andrea Jackowsi, PhD, Federal University of São Paulo
- Principal Investigator: Jonathan Posner, MD, Duke University
- Study Director: Tenneill Murray, MPH, New York State Psychiatric Institute
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB #8245/Pro00077397
- 1R01MH128937-01 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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