Mental Disorders Clinical Trial
Official title:
Addressing Mental Health Disparities in Refugee Children: A CBPR Collaboration
Verified date | July 2019 |
Source | Boston College |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will use CBPR mixed methods (qualitative and quantitative data collection) to conduct needs assessments and design and evaluate a core family-based intervention. Project activities will emphasize capacity building in two refugee communities resettled in Greater Boston—the Somali Bantu and the Bhutanese—actively engaging refugee community members, community advisory boards, services providers, and other stakeholders. Specific Aims are to: (1) deepen partnerships with the Somali Bantu and Bhutanese communities through co-leadership, capacity-building, and knowledge sharing; (2) collect and apply qualitative data to (a) prepare a needs assessment of mental health in children and adolescents, barriers to care, and services preferences with each target refugee group; (b) develop mental health/psychosocial assessments for refugee caregivers and children; (c) adapt the core components of a family-based strengthening intervention for use with refugees; and (3) conduct an 80-family pilot study to examine acceptability and sustainability of the intervention. Key outcomes will be reduced mental health symptoms among children and adolescents and improvement in caregiver-child relationships.
Status | Completed |
Enrollment | 265 |
Est. completion date | April 2019 |
Est. primary completion date | February 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 5 Years and older |
Eligibility |
Inclusion Criteria: - Refugee families must have a school-aged child (aged 5-17), and caregivers must be at least 18 years of age and live in the same household as the child. Exclusion Criteria: - Untreated mental illness or active family crisis |
Country | Name | City | State |
---|---|---|---|
United States | Chelsea Collaborative | Chelsea | Massachusetts |
United States | Jewish Family Service | Springfield | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Boston College | National Institute on Minority Health and Health Disparities (NIMHD) |
United States,
Betancourt TS, Frounfelker R, Mishra T, Hussein A & Falzarano R. American Journal of Public Health. Published on-line ahead of print April 23, 2015; e1-8. doi:10.2105/AJPH.2014.302504
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in depressive symptoms among children and adolescents | Depressive symptoms will be measured with an adapted version of the Center for Epidemiologic Study-Depression) CES-D scale | Depressive symptoms will be measured at three time points - at baseline prior to intervention, immediately post-intervention (an average of 16 weeks after baseline), and 6 months after the completion of the intervention | |
Secondary | Change in anxiety symptoms among children and adolescents | Anxiety symptoms will be measured with an adapted version of the CES-D | Anxiety symptoms will be measured at three time points - at baseline prior to intervention, immediately post intervention (an average of 16 weeks after baseline), and six months after the completion of the intervention | |
Secondary | Change in externalizing/behavioral problems among children and adolescents | Externalizing symptoms will be measured with the (Youth Self-Report) YSR externalizing sub scale | Externalizing symptoms will be measured at three time points - at baseline prior to intervention, immediately post-intervention (an average of 16 weeks after the baseline), and 6 months after the completion of the intervention | |
Secondary | Change in parent-child relationships | Parent-child relationships will be measured with an adapted version of the Alabama parenting scale | Quality of parent-child relationships will be measured at three time points - at baseline prior to intervention, immediately post-intervention (an average of 16 weeks after the baseline), and 6 months after the completion of the intervention. |
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