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Reintegration of Children From Institutions in Azerbaijan

Primary Purpose

Emotional Trauma, Child Mental Disorder, Child Maltreatment

Status
Recruiting
Phase
Not Applicable
Locations
Azerbaijan
Study Type
Interventional
Intervention
Usual Care
Family Strengthening
Mental Health Screening, Referral and Connection to Services
Economic Empowerment
Sponsored by
University of Chicago
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Emotional Trauma focused on measuring Azerbaijan, Children, Child Mental Health, Family Strengthening, Economic Empowerment, Child and Family Well-being, Child Separation, Child Maltreatment

Eligibility Criteria

7 Years - 12 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. The child is between ages 7 and 12;
  2. The caregiver is at least 18 years old;
  3. The child has a history of institutionalization (lived in an orphanage or another institution in Azerbaijan for a minimum of one month);
  4. The child has been reunited with a caregiver (biological parent or kin relative) within a year prior to the study;
  5. The child has a caregiver who is a biological parent or kin relative (e.g., grandparent) who serves as the primary caregiver;
  6. The child and caregiver can commit to study participation.

Exclusion Criteria:

  1. Child is not between the ages of 7-12.
  2. Caregiver is below the age of 18.
  3. Eligible child and/or caregiver cannot commit to study participation.
  4. Children or caregivers with significant cognitive, behavioral, and/ or mental health impairment (e.g., severe developmental disorder, psychosis, severe symptoms of trauma) that may interfere with their ability to consent to and/or benefit from the program or to participate safely will also be excluded from the study.

Sites / Locations

  • National Mental Health CentreRecruiting
  • SOS Children's Villages Azerbaijan

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm 8

Arm Type

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Arm Label

Family Strengthening, Mental Health, Economic Empowerment

Family Strengthening, Mental Health

Family Strengthening, Economic Empowerment

Family Strengthening Only

Mental Health, Economic Empowerment

Mental Health Only

Economic Empowerment Only

Usual Care Only

Arm Description

Group will receive: 1) Usual Care, 2) Family Strengthening, 3) Mental Health Screening & Referral, and 4) Economic Empowerment Interventions

Group will receive: 1) Usual Care, 2) Family Strengthening, and 3) Mental Health Screening & Referral Interventions

Group will receive: 1) Usual Care, 2) Family Strengthening, and 3) Economic Empowerment Interventions

Group will receive: 1) Usual Care and 2) Family Strengthening Interventions

Group will receive: 1) Usual Care, 2) Mental Health Screening & Referral, and 3) Economic Empowerment Interventions

Group will receive: 1) Usual Care and 2) Mental Health Screening & Referral Interventions

Group will receive: 1) Usual Care and 2) Economic Empowerment Interventions

Group will receive: Usual Care Intervention only

Outcomes

Primary Outcome Measures

Change in child mental health measured using the Strengths and Difficulties Questionnaire (SDQ)
Questions assess child's internalizing problems (depression, anxiety) and externalizing problems (aggressive or disruptive behavior). SDQ includes five scales: emotional symptoms, conduct problems, hyperactivity/inattention, peer relationship problems, and prosocial behaviors reported by parent/caregiver and teacher. With the exception of prosocial behaviors, lower score indicates reduction in mental health symptoms.
Changes in child self-reported symptoms of depression using the Center for Epidemiological Studies Depression Scale for Children (CES-DC)
The Center for Epidemiological Studies Depression Scale for Children (CES-DC) is a 20 item self-report questionnaire for young people between the ages of 6 and 17. Possible scores ranging from 0 to 60 and lower score indicates a reduction in depressive symptoms.
Changes in child's post-traumatic symptoms using the Revised Child Impact of Events Scale
Revised Child Impact of Events Scale (CRIES-8) is a 8-item child-friendly measure designed to screen children at risk for Post-Traumatic Stress Disorder (PTSD). the CRIES-8 has two sub-scales (Intrusion and Avoidance). Total scores range from 0 to 40, with higher scores indicated higher PTSD symptoms. A reduction in trauma symptoms would indicate improvement.

Secondary Outcome Measures

Change in supportive parenting
The use of harsh parenting practices and level of parental support using Parenting Styles & Dimensions Questionnaire - Short version (PSDQ-Short Version). The scale includes 32 items and can be grouped into three styles and seven dimensions of parenting (e.g., physical coercion, verbal hostility, and punishment; support and affection, regulation, and autonomy). The score in all dimensions and styles ranges from 1 to 5, with higher scores indicating more use of its dimensions or styles.
Change in parental stress
The parental level of distress is measured using the Depression Anxiety Stress Scale - 21 items / DASS-21). The Depression, Anxiety and Stress Scale - 21 Items (DASS-21) is a set of three self-report scales designed to measure the emotional states of depression, anxiety and stress. The scores for each of three sub-scales range from 0 to 42. Lower DASS score would indicate a reduction in the level of stress and anxiety among parents.
Changes in savings
Monthly savings in the Child Savings Accounts are collected through participant's bank statements. Higher average monthly saving amount would indicate improvement.

Full Information

First Posted
May 19, 2022
Last Updated
May 24, 2022
Sponsor
University of Chicago
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Mental Health Centre, SOS Children's Villages Azerbaijan
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1. Study Identification

Unique Protocol Identification Number
NCT05396625
Brief Title
Reintegration of Children From Institutions in Azerbaijan
Official Title
Optimizing Prevention Approaches for Children Reintegrating From Orphanages in Azerbaijan
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2021 (Actual)
Primary Completion Date
June 30, 2024 (Anticipated)
Study Completion Date
June 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Chicago
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Mental Health Centre, SOS Children's Villages Azerbaijan

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To prevent mental health problems among 7-12 children from orphanages reunited with their biological or extended families in Azerbaijan, this study will refine and test three evidence-based intervention approaches (a) family strengthening intervention; b) mental health screening and referral for treatment; and c) economic empowerment in the form of Child Savings Accounts). The study will use a randomized experimental design and participating families will be assigned to receive the family strengthening, mental health, or economic interventions. Eligible and consenting 400 child-caregivers dyads will complete baseline, 1-year, and 2-year follow-up measures. Additionally, post-intervention qualitative interviews (n=60) will solicit narrative information about participants' and services providers' reactions and experiences with each intervention component and will provide more comprehensive evidence about the interventions' efficacy. It is hypothesized that by enhancing children's coping skills, strengthening child-parent relationships, and reducing parental stress, an intervention can help children demonstrate fewer symptoms of: a) disturbances of attachment; b) internalizing problems (depressive or anxious mood), c) externalizing problems (aggressive, delinquent, or disruptive behaviors); d) post-traumatic stress; and e) lower prevalence of diagnoses (e.g. depression, anxiety, PTSD, oppositional-defiant disorder, and reactive attachment disorder).
Detailed Description
The countries of the former Soviet Union (fSU) and Eastern Europe have the highest number of children in institutional care worldwide--up to 1.3 million children. Institutional care is associated with severe developmental setbacks and poor mental health outcomes for children, and many fSU countries are looking to develop reintegration programs supported by evidence. Acknowledging the detrimental effects of institutionalization on children, the government of Azerbaijan jointly with UNICEF is implementing a national de-institutionalization program (De-I) aiming to close down orphanages and place children in family-oriented care. The De-I program provides basic case management services to reunite children with their families of origin, but does not address mental health needs of institutionalized children, who after years of isolation, maltreatment and traumatic experiences in orphanages, are returning home to parents who are unprepared to deal with the emotional and behavioral problems of their children. In addition, the current De-I model does not address the family-level poverty which led to institutionalization in the first place, creating a risk for future abandonment and poor psychosocial outcomes. This study focuses on building research capacity in the field of global mental health to identify effective prevention strategies and develop innovative psychosocial intervention models tailored to the local context of post-Soviet countries. According to the NIMH Grand Challenges in Global Mental Health, advancement of prevention and implementation of early interventions (Goal B) is among the key global mental health priorities. Early prevention reduces the risk of developing mental disorders in adulthood, has long-term impact and may concurrently affect a number of psychosocial outcomes. There are no evidence-based, culturally-tailored, preventive mental health interventions available for institutionalized children in Azerbaijan and other fSU countries. Existing interventions in the U.S. often require highly skilled clinicians and are not adapted for the context of developing countries with limited financial and human mental health resources. Effective parenting and behavior management skills are essential for preventing emotional and behavioral problems among children. However, in low-resource settings, non-parenting factors such as poverty induced parental stress have also been linked to poor child mental health outcomes and cannot be addressed by parenting skills programs alone. Based on the formative research conducted by the investigative team (2014-2018) in collaboration with a local Community Collaborative Board (CCB), we selected and adapted empirically-tested intervention components to ensure their cultural relevance, viability and inexpensive delivery, essential for developing countries. To promote family stability and improve the emotional well-being among children reuniting with psychosocial functioning of institutionalized children, the proposed intervention will include three components: a) a family-strengthening program, b) referral and access to mental health treatment; and c) economic empowerment. The proposed study will test these intervention components with 400 child-parent dyads in a trial using the Multiphase Optimization Strategy (MOST) to compare different intervention components and identify the most optimal combination. If efficacious, the optimized intervention may enhance the traditional De-I model and be scaled up throughout Azerbaijan and other fSU countries. The specific aims of the research study within the R01 mechanism are: Aim 1: To refine, test and compare the effects of three intervention components (family strengthening intervention; referral and access to mental health treatment; and economic empowerment) on mental health outcomes (a) post-traumatic symptoms; b) disturbances of attachment; c) internalizing problems--depression, anxiety; and d) externalizing problems--aggressive or disruptive behavior) among 7-12 year old children from orphanages re-entering family contexts in Azerbaijan. Aim 2: To examine the role of hypothesized intervention mediators (emotion regulation, supportive parenting, and parental stress) and moderators (child's age, gender, length in institution, family structure, and intervention adherence) in improvements in child mental health outcomes. Aim 3: To explore facilitating factors and barriers to implementation and participation in each intervention component (at individual, family, and organizational levels) using qualitative interviews with intervention participants and service providers. We will also conduct a secondary analysis to estimate the preliminary costs (operations and personnel) of each intervention component compared to the usual care alone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Emotional Trauma, Child Mental Disorder, Child Maltreatment
Keywords
Azerbaijan, Children, Child Mental Health, Family Strengthening, Economic Empowerment, Child and Family Well-being, Child Separation, Child Maltreatment

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Model Description
The study will use a randomized design and apply MOST approach to test and compare the three intervention components: a) a family-strengthening intervention; b) mental health screening and referral for treatment; and c) economic empowerment in the form of Child Savings Accounts /CDAs. There are three factors (intervention components) and each factor has two levels. This is a 2*2*2, or 2 by 3, factorial design and, therefore, the study will have eight different experimental conditions or groups (2 by 3=8). The eligible and consenting child-parent dyads (N=400) will be randomly assigned to one of eight study groups (50 dyads per group), determining how many and which intervention components participants will receive. Given this design, half of the sample (n=200) will receive each intervention component (e.g., families assigned to Groups 1-4 will receive the family strengthening intervention and will be compared to families from Groups 5-8). All participants will receive Usual Care.
Masking
Outcomes Assessor
Masking Description
The eligible and consenting child-caregiver dyads will be randomized into one of eight experimental conditions. The randomization will be performed by the Project Director immediately following the baseline visit. A secure, web-based, password-protected database built on a REDCap (Research Electronic Data Capture) platform will be used to randomize participants into the 8 experimental conditions and to manage recruitment; eligibility assessment; scheduling and tracking of baseline and follow-up assessments; and sending intervention reminders. All data collectors (or interviewers) will receive a highly structured and intensive interview training conducted by the PIs. Data collectors and outcome assessors will be masked to participants' intervention group assignment.
Allocation
Randomized
Enrollment
400 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Family Strengthening, Mental Health, Economic Empowerment
Arm Type
Experimental
Arm Description
Group will receive: 1) Usual Care, 2) Family Strengthening, 3) Mental Health Screening & Referral, and 4) Economic Empowerment Interventions
Arm Title
Family Strengthening, Mental Health
Arm Type
Experimental
Arm Description
Group will receive: 1) Usual Care, 2) Family Strengthening, and 3) Mental Health Screening & Referral Interventions
Arm Title
Family Strengthening, Economic Empowerment
Arm Type
Experimental
Arm Description
Group will receive: 1) Usual Care, 2) Family Strengthening, and 3) Economic Empowerment Interventions
Arm Title
Family Strengthening Only
Arm Type
Experimental
Arm Description
Group will receive: 1) Usual Care and 2) Family Strengthening Interventions
Arm Title
Mental Health, Economic Empowerment
Arm Type
Experimental
Arm Description
Group will receive: 1) Usual Care, 2) Mental Health Screening & Referral, and 3) Economic Empowerment Interventions
Arm Title
Mental Health Only
Arm Type
Experimental
Arm Description
Group will receive: 1) Usual Care and 2) Mental Health Screening & Referral Interventions
Arm Title
Economic Empowerment Only
Arm Type
Experimental
Arm Description
Group will receive: 1) Usual Care and 2) Economic Empowerment Interventions
Arm Title
Usual Care Only
Arm Type
Experimental
Arm Description
Group will receive: Usual Care Intervention only
Intervention Type
Behavioral
Intervention Name(s)
Usual Care
Intervention Description
All participants will receive the following services: case management and psychosocial support (e.g., assessment and identification of families eligible for reunification; preparing children and parents for reunification; and assistance with receiving social benefits such as Targeted Social Assistance, alimonies, or disability benefits); referrals to schools outside of their orphanage; and leisure activities for children (e.g., music, sport, and drama) provided by the orphanage staff and municipal social services.
Intervention Type
Behavioral
Intervention Name(s)
Family Strengthening
Other Intervention Name(s)
SAFE Children
Intervention Description
Due to its focus on family-strengthening, the study uses the evidence-based intervention 'SAFE Children,' which employs a multiple family group format and is designed to improve family functioning, strengthen child-parent relationships and communication, enhance supportive parenting strategies, and prevent emotional and behavioral problems among at-risk children. The family-focused intervention consists of weekly multiple family group meetings (e.g. about 5 families per group). All interested family members are invited to join the sessions. The adapted intervention incorporates new sessions that address unique issues faced by families reuniting with formerly institutionalized children (e.g., separation and attachment issues, children's feelings of resentment, parents' feelings of guilt and shame, stigmatized status in the community). Each session lasts about one to one and a half hours and will be delivered by facilitator and co-facilitator at the SOS Child and Family Center.
Intervention Type
Behavioral
Intervention Name(s)
Mental Health Screening, Referral and Connection to Services
Intervention Description
Children assigned to this intervention will receive clinical assessment performed by psychiatrists at the National Mental Health Centre in Azerbaijan. From there, each child will have an individual plan developed by the multidisciplinary team and will be connected to the National Mental Health Centre clinicians to receive corresponding mental health services.
Intervention Type
Other
Intervention Name(s)
Economic Empowerment
Intervention Description
The economic component will be in the form of Child Development Accounts/CDAs, an asset-based strategy encouraging savings and investment. This component will connect families to a bank and train them on how to save small amounts, which will be matched by contributions from the project. Matched savings will be deposited in a separate account and can be used only towards a child's education or for housing. The project will provide $50 as seed money to open a savings account in the child's name. The child's family members will make small monthly contributions to the CDA, and savings of up to $20 per month will be matched with project funds at a rate of 2:1. Caregivers will also receive training on savings and financial planning. The curriculum will be taught by trainers from the SOS in a group format for 5 sessions and will cover these topics: The Importance of Saving; Identifying and Managing Resources; Setting Up a Savings System; Sources of Income; and Budgeting and Spending.
Primary Outcome Measure Information:
Title
Change in child mental health measured using the Strengths and Difficulties Questionnaire (SDQ)
Description
Questions assess child's internalizing problems (depression, anxiety) and externalizing problems (aggressive or disruptive behavior). SDQ includes five scales: emotional symptoms, conduct problems, hyperactivity/inattention, peer relationship problems, and prosocial behaviors reported by parent/caregiver and teacher. With the exception of prosocial behaviors, lower score indicates reduction in mental health symptoms.
Time Frame
Baseline, 12 months, 24 months
Title
Changes in child self-reported symptoms of depression using the Center for Epidemiological Studies Depression Scale for Children (CES-DC)
Description
The Center for Epidemiological Studies Depression Scale for Children (CES-DC) is a 20 item self-report questionnaire for young people between the ages of 6 and 17. Possible scores ranging from 0 to 60 and lower score indicates a reduction in depressive symptoms.
Time Frame
Baseline, 12 months, 24 months
Title
Changes in child's post-traumatic symptoms using the Revised Child Impact of Events Scale
Description
Revised Child Impact of Events Scale (CRIES-8) is a 8-item child-friendly measure designed to screen children at risk for Post-Traumatic Stress Disorder (PTSD). the CRIES-8 has two sub-scales (Intrusion and Avoidance). Total scores range from 0 to 40, with higher scores indicated higher PTSD symptoms. A reduction in trauma symptoms would indicate improvement.
Time Frame
Baseline, 12 months, 24 months
Secondary Outcome Measure Information:
Title
Change in supportive parenting
Description
The use of harsh parenting practices and level of parental support using Parenting Styles & Dimensions Questionnaire - Short version (PSDQ-Short Version). The scale includes 32 items and can be grouped into three styles and seven dimensions of parenting (e.g., physical coercion, verbal hostility, and punishment; support and affection, regulation, and autonomy). The score in all dimensions and styles ranges from 1 to 5, with higher scores indicating more use of its dimensions or styles.
Time Frame
Baseline, 12 months, 24 months
Title
Change in parental stress
Description
The parental level of distress is measured using the Depression Anxiety Stress Scale - 21 items / DASS-21). The Depression, Anxiety and Stress Scale - 21 Items (DASS-21) is a set of three self-report scales designed to measure the emotional states of depression, anxiety and stress. The scores for each of three sub-scales range from 0 to 42. Lower DASS score would indicate a reduction in the level of stress and anxiety among parents.
Time Frame
Baseline, 12 months, 24 months
Title
Changes in savings
Description
Monthly savings in the Child Savings Accounts are collected through participant's bank statements. Higher average monthly saving amount would indicate improvement.
Time Frame
Baseline, 12 months, 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: The child is between ages 7 and 12; The caregiver is at least 18 years old; The child has a history of institutionalization (lived in an orphanage or another institution in Azerbaijan for a minimum of one month); The child has been reunited with a caregiver (biological parent or kin relative) within a year prior to the study; The child has a caregiver who is a biological parent or kin relative (e.g., grandparent) who serves as the primary caregiver; The child and caregiver can commit to study participation. Exclusion Criteria: Child is not between the ages of 7-12. Caregiver is below the age of 18. Eligible child and/or caregiver cannot commit to study participation. Children or caregivers with significant cognitive, behavioral, and/ or mental health impairment (e.g., severe developmental disorder, psychosis, severe symptoms of trauma) that may interfere with their ability to consent to and/or benefit from the program or to participate safely will also be excluded from the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Leyla Ismayilova, PhD
Phone
773-834-0401
Email
leyla@uchicago.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leyla Ismayilova, PhD
Organizational Affiliation
University of Chicago
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Mental Health Centre
City
Baku
Country
Azerbaijan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Narmin Guliyeva, MD
First Name & Middle Initial & Last Name & Degree
Fuad Ismayilov, MD
Facility Name
SOS Children's Villages Azerbaijan
City
Baku
Country
Azerbaijan
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rashad Huseynov

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Datasets will be made available to any individual who makes a direct request to the PIs and indicates the data will be used for the purposes of research (per CFR Title 45 Part 46: "Research is defined as a systematic investigation, including research development, testing and evaluation, designed to develop or contribute to generalizable knowledge."). Shared data will be free of identifiers that would permit linkages to individual research participants and variables that could lead to deductive disclosure of the identity of individual subjects. Data will be shared in electronic format native to the software used by the Investigators; requestors are expected to handle converting electronic formats (though the Investigators will consider converting to tab-delimited text format if possible).
IPD Sharing Time Frame
Once all of the data have been de-identified, cleaned, and validated, and main findings have been published, the Investigators expect to share data with the scientific community. Upon completion of the deliverable(s), the requestor will be instructed to destroy all copies of the data. If deliverables have not been produced yet, the agreement to share data will be revisited annually to decide to continue sharing or terminate the sharing agreement. If the Investigators determine that the sharing agreement should be terminated, the requestor will be instructed to destroy all copies of the data.
IPD Sharing Access Criteria
The University of Chicago has a data sharing agreement that specifies the following conditions be met before data are shared: A formal research question is specified a priori; Names, affiliations, and roles of any other individuals who will access the shared data; The deliverable(s)-e.g., manuscript, conference presentation-are specified a priori; Proper credit and attribution-e.g., authorship, co-authorship, and order-for each deliverable are specified a priori; A statement indicating an understanding that the data can not be further shared with any additional individual(s) or parties without the PI's permission; IRB approval for use of the data (or documentation that IRB has determined the research is exempt);

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Reintegration of Children From Institutions in Azerbaijan

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