Impacts of Cash Transfers on Child Neurodevelopment (Auxilio Brasil)

Sponsor
New York State Psychiatric Institute (Other)
Overall Status
Recruiting
CT.gov ID
NCT05477901
Collaborator
National Institute of Mental Health (NIMH) (NIH)
450
2
2
63
225
3.6

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Supplemental cash transfer
N/A

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 Design

Study Type:
Interventional
Anticipated Enrollment :
450 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Post-baseline Procedure -- Random Assignment to Intervention After baseline, 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 and remains in their study arm throughout the study after randomizationPost-baseline Procedure -- Random Assignment to Intervention After baseline, 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 and remains in their study arm throughout the study after randomization
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Mental Health and Bolsa Familia: A Mechanistically Focused Clinical Trial of a Cash Transfer Intervention on Child Brain, Behavior, and Mental Health
Anticipated Study Start Date :
Sep 1, 2022
Anticipated Primary Completion Date :
Aug 1, 2026
Anticipated Study Completion Date :
Dec 1, 2027

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

High supplemental transfer: $40 a month

Other: Supplemental cash transfer
Supplemental cash transfer ($40/month)

No Intervention: Control

Low supplemental transfer: $2 a month

Outcome Measures

Primary Outcome Measures

  1. Adverse Childhood Experiences (ACEs) - FHE [Baseline]

    Family History Epidemiologic screener is a 9-item (+subitems) checklist to asses child's ACEs, more checked items mean more ACEs.

  2. Changes in Adverse Childhood Experiences (ACEs) - FHE [8 months]

    Family History Epidemiologic screener is a 9-item (+subitems) checklist to asses child's ACEs, more checked items mean more ACEs.

  3. Changes in Adverse Childhood Experiences (ACEs) - FHE [16 months]

    Family History Epidemiologic screener is a 9-item (+subitems) checklist to asses child's ACEs, more checked items mean more ACEs.

  4. Changes in Adverse Childhood Experiences (ACEs) - FHE [24 months]

    Family History Epidemiologic screener is a 9-item (+subitems) checklist to asses child's ACEs, more checked items mean more ACEs.

  5. Changes in Adverse Childhood Experiences (ACEs) - FHE [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. Adverse Childhood Experiences (ACEs) - CTC [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.

  7. Changes in Adverse Childhood Experiences (ACEs) - CTC [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. Changes in Adverse Childhood Experiences (ACEs) - CTC [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.

  9. Changes in Adverse Childhood Experiences (ACEs) - CTC [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.

  10. Changes in Adverse Childhood Experiences (ACEs) - CTC [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.

  11. Child internalizing and externalizing symptoms [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.

  12. Changes in Child internalizing and externalizing symptoms [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.

  13. Changes in Child internalizing and externalizing symptoms [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.

  14. Changes in Child internalizing and externalizing symptoms [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.

  15. Changes in Child internalizing and externalizing symptoms [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.

  16. Access to health care [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.

  17. Changes in Access to health care [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.

  18. Changes in Access to health care [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.

  19. Changes in Access to health care [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.

  20. Child brain MRI scan [Baseline]

    Child participants will undergo an MRI scan (~1 hour) to examine the function and connectivity of EF-related brain systems

  21. Changes in Child brain MRI scan [24 months]

    Child participants will undergo an MRI scan (~1 hour) to examine the function and connectivity of EF-related brain systems

  22. Child Executive Function [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.

  23. Changes in Child Executive Function [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. Changes in Child Executive Function [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.

  25. Biospecimen - Child hair sample [Baseline]

    Child hair samples to measure HPA activity (cortisol)

  26. Biospecimen - Changes in Child hair sample [24 months]

    Child hair samples to measure HPA activity(cortisol)

  27. Biospecimen - Blood Draw - IL-6 [Baseline]

    Primary immune measures will consist of IL-6 and CRP, consistent with prior research on inflammation and neurodevelopment.

  28. Biospecimen - Blood Draw - Change in IL-6 [24 months]

    Primary immune measures will consist of IL-6 and CRP, consistent with prior research on inflammation and neurodevelopment.

  29. Biospecimen - Blood Draw - CRP [Baseline]

    Primary immune measures will consist of IL-6 and CRP, consistent with prior research on inflammation and neurodevelopment.

  30. Biospecimen - Blood Draw - Change in CRP [24 months]

    Primary immune measures will consist of IL-6 and CRP, consistent with prior research on inflammation and neurodevelopment.

  31. Family Adaptability and Cohesion Evaluation Scale-III (FACES-III) [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.

  32. Change in Family Adaptability and Cohesion Evaluation Scale-III (FACES-III) [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.

Secondary Outcome Measures

  1. Food insecurity [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.

  2. Changes in Food insecurity [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.

  3. Home observation/environment [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.

  4. Changes in Home observation/environment [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
23 Years to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Mother:
Inclusion Criteria:
  1. Age 23-45 years old

  2. Receiving AB cash transfers

  3. Has at least one child ages 7-10 years old at time of recruitment

  4. Able to consent

Exclusion Criteria:
  1. Mother and child do not reside in same household
Child:

Inclusion Criterion

  1. Age 7-10 years old

  2. IQ > 80

Exclusion Criterion

  1. Does not reside in same household as the mother

  2. Major Axis I disorder (e.g., Autism, Schizophrenia, Bipolar), ADHD and disruptive behavior disorders will not be exclusionary because of their high prevalence

  3. MRI contradictions

Contacts and Locations

Locations

Site City State Country Postal Code
1 New York State Psychiatric Institute New York New York United States 10032
2 UNIFESP São Paulo SP Brazil 04023

Sponsors and Collaborators

  • New York State Psychiatric Institute
  • National Institute of Mental Health (NIMH)

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 Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Cristiane Duarte, Ruane Professor for the Implementation of Science for Child and Adolescent mental Health (in Psychiatry) at CUMC, New York State Psychiatric Institute
ClinicalTrials.gov Identifier:
NCT05477901
Other Study ID Numbers:
  • IRB #8245
  • 1R01MH128937-01
First Posted:
Jul 28, 2022
Last Update Posted:
Jul 28, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 28, 2022