• Skip to primary navigation
  • Skip to main content
  • Skip to footer
NNED – National Network to Eliminate Disparities in Behavioral Health

NNED - National Network to Eliminate Disparities in Behavioral Health

  • News & Events
    • News & Announcements
    • Upcoming Events
  • Opportunities
    • Funding
      • Funding Opportunities
      • National & Local Foundations
    • Professional Development
    • NNEDLearn
  • Connect
    • Partner Central
    • National Behavioral Health Consultants and Experts Group
  • Resources
    • NNEDshare
    • Webinars
  • Join the NNED
    • Member Login
    • Join the NNED
    • About the NNED

News

Harris County Protective Services: Integrating a Fragmented System of Care

October 11, 2017

It is estimated that 40-60% of children in state care have behavioral health problems, which are often accompanied by physical health concerns as well.

In 2012, approximately 4,800 children in Harris County, TX were placed into protective custody programs. These children come from a variety of backgrounds and experiences, and are placed in the care of foster parents, kinship placements or other caretaking scenarios. Harris County Protective Services (HCPS) has provided children in state custody with physical health checks, full dental exams, x-rays and pharmaceutical services since the 1970s. However, 100 percent of mental health and behavioral health cases were referred out. The majority of children in kinship care in Harris County (56 percent) did not receive behavioral health treatment. “Kids weren’t being screened. They often went without assessment and treatment for mental health issues, and conditions worsened,” says Jacquelyn M. McMillon, Children’s Services Administrator at HCPS.

Since Medicaid became available to children in state custody, use of the HCPS medical clinics began dwindling. It was clear that their current model needed re-evaluating and they sought a better health care approach for children.

Laying the Groundwork for Success

HCPS received funding from the Hogg Foundation to implement an integrated health care program for children ages birth through 17 in state care. The program attempted to address gaps in services for children in foster care, who tend to have much higher rates of mental health concerns, physical health concerns, and developmental delays than children from similar socioeconomic circumstances.

The grant included a planning phase during which HCPS put together a steering committee to discuss the clinic and its services, and gather information from a broad stakeholder group including kinship caregivers, foster parents, alumni of the CPS system, parent partners, parent representatives, and organizations related to child abuse and neglect.

Three Services Under One Roof

McMillon and her team began to identify exactly how they wanted the clinic to look. Over that first year, they were able to develop a plan that became an integrated health care model for children in the child welfare system. They began by hiring a care manager and a child psychiatrist, and adding a psychiatric and behavioral health component to the existing model of medical and dental care. By putting all three services under one roof, HCPS created vital communication flows between medical, dental and behavioral health. They were able to make referrals within one setting, while also working with caregivers and children for specialty care and referrals outside of the system.

Family-Centered Support

HCPS understood that families needed very basic support and were stressed by the system. In response, HCPS created a Family Support Navigator position funded by a grant from the Harris County Hospital District Foundation. The Family Support Navigator has personal, lived experience, having been involved with child protective services, worked through the system, or had a child with behavioral health issues.

Initial Success

Results from the pilot program point to an extremely promising approach with clear, early results. Following the initial planning phase, HCPS successfully launched their integrated health care initiative in June 2014, creating a program in which:

  • Care management and psychiatric services are provided on-site and in collaboration with primary care
  • 194 unique clients were served as of September 2015
  • There has been an increase in patient satisfaction and number of visits
  • Caregivers and stakeholders report that the program fills important service gaps (e.g. care management and psychiatric services).

The integrated health care project provides comprehensive health care to children in kinship and foster care, allows caregivers to focus on prevention and wellness, and results in better health outcomes.

Learn more at Hogg.UTexas.edu.

Filed Under: News

Home Visits Help Strengthen Maternal, Infant Health in Native American Communities

October 10, 2017

A baby’s first laugh, in Navajo culture, is cause for formal celebration. Whoever provokes that milestone moment wins the privilege of hosting a “first laugh ceremony” to mark the infant’s full arrival into the earthly world. “That laugh sounds to the world, ‘This is me and this is who I am,'” says Crystal Kee, a Navajo health educator based in Chinle, Arizona. Though the tradition is unique to the Navajo, Kee finds it resonates across a variety of American Indian communities that take part in Family Spirit, a home-visiting program that supports maternal and infant health. “There is a thirst for some connection to the culture, and the ways our ancestors and people have always thought,” says Kee, who works as a training and implementation manager for Family Spirit.

The program was designed both for and by Native tribal communities. It grew out of the Johns Hopkins Center for American Indian Health in the mid-1990s, when program leaders began working in partnership with the Navajo Nation and White Mountain Apache and San Carlos Apache tribes. Today Family Spirit is active in more than 100 tribal communities across 16 states, with the Hopkins center—part of the Bloomberg School of Public Health—disseminating the model to affiliate health centers and organizations.

The program trains people from the local community to deliver regular one-on-one home visits to mothers (and often fathers, too) from pregnancy through the first three years of the child’s life. The general goal is to share best practices for parenting and early childhood health, covering topics like budgeting and breastfeeding. But because the program is so personalized, it often wades into deeper issues the families are facing, such as employment challenges or drug abuse. Kee notes that opioid and methamphetamine problems are on the rise for tribal communities, requiring “patience and care” from Family Spirit home visitors while they “remain neutral.” And since many participants in Family Spirit are still in their teens and early 20s, the program often grapples with the risks and complexities of parenting at a young age.

With evidence showing successful outcomes—including decreases in depression and emotional problems for mothers, and reduced behavioral problems for their children—Family Spirit has expanded over the years beyond its initial rural settings in Arizona and New Mexico. It’s now used in several urban communities with American Indian populations, including in Oakland, California, and Oklahoma City.

Beyond that, the program is showing promise even for non-tribal communities—an adapted model has served low-income, predominantly black or Latino populations at sites in St. Louis and Chicago, according to Kee. “We get a lot of requests for translating the curriculum into Spanish,” she says.

In addition to reaching out to other populations, Nicole Neault, a field manager for Family Spirit, says future directions may include digitizing the curriculum and continuing to build an offshoot model, Family Spirit Nurture, that targets childhood obesity.

Learn more at HUB, Johns Hopkins University’s news center.

Filed Under: News

National Latinx AIDS Awareness Day (Oct. 15th)

October 10, 2017

October 15 is National Latinx AIDS Awareness Day (NLAAD). The 2017 NLAAD theme is “To Defeat HIV You’re a Superhero. Use Your Superpowers.”

The Latino Commission on AIDS (LCOA), the Hispanic Federation and other organizations organize this day to build capacity for non-profit organizations and health departments to reach Latino/Hispanic communities, promote HIV testing, and provide HIV prevention information and access to care.

Hispanic/Latinos in the United States (US) are disproportionately impacted by HIV/AIDS. They represent 18% of the US population yet accounted for almost 1 in 4 (24%) infections among adults and adolescents in 2015.1 Factors such as lack of health insurance, language barriers, lack of familiarity with the US healthcare system and stigma often limit the health care access of Hispanics/Latinos in the US, thereby limiting opportunities for HIV/AIDS screening and treatment. Given that Hispanics/Latinos are the largest and fastest growing minority group in the US, addressing HIV/AIDS in their community is important to the nation’s health. At the end of 2014, there were roughly 216,000 Hispanic/Latinos living with HIV in the U.S. but only 27% of the 85% that were diagnosed and aware of their affliction achieved viral suppression.

Learn about the Epidemic

  • HIV Testing and Outcomes Among Hispanics/Latinos
  • HIV Among Hispanics/Latinos
  • Today’s HIV/AIDS Epidemic (pdf) from the CDC
  • Become more informed through HIV.gov’s HIV Basics Guide

Find HIV Testing and other Services

  • HIV Testing Sites & Care Services Locator
  • Add the locator widget to your website
  • Download the mobile app on your iPad, iPhone or Android device
  • Visit the CDC’s GetTested site for testing, questions, and more resources

Graphics

  • Get NLAAD 2017 Posters, Infographics, Social Media Resources, Web Banners, Logos, and Themes from the Latino Commision on AIDS
  • Download the badge (png)
  • Get Social Media Images, Posters, and Infographics in Spanish and English from the CDC

Get Involved

  • Register with NLADD to list your events and find other nearby events
  • Read the National HIV/AIDS Strategy: Updated to 2020 (pdf)
  • Lee Estrategia Nacional Contra El VIH/SIDA para los Estados Unidos: Actualizada Hasta 2020(pdf)

More Resources

  • Doing It
  • Start Talking. Stop HIV.
  • Let’s Stop HIV Together
  • Visit: Office of Minority Health, Infosida, Learn the Link: Drugs and HIV

Learn more at HIV.gov.

Filed Under: News

Powering Health Equity Action with Online Data Tools: 10 Design Principles

October 9, 2017

PolicyLink and EcoTrust recently released a report that aims to strengthen community-driven efforts to achieve health equity by improving the online data tools that make health equity data readily available to them.

Achieving health equity—when everyone has a just and fair opportunity to be as healthy as possible regardless of race, income, or other socially defined characteristics—is essential to building resilient communities, a prosperous economy, and a just society. Without optimal health, it is impossible for people to reach their full potential. Yet today in the United States, health disparities are persistent and growing. These inequities are not natural or inevitable, but stem from structural racism and discrimination, as well as the inequitable policies, practices, and resource allocations that create the vastly unequal conditions in which people live

Community-based organizations play a crucial role in advancing health equity. These institutions help put in place new policies, plans, and programs that improve neighborhood environments and opportunities for low-income communities, communities of color, and others unjustly and unfairly burdened by poor health. And community-level data that is disaggregated by race, income, neighborhood, and other demographics is an essential tool to increase the effectiveness and impact of these organizations.

Robust local data can help community groups at every stage of the policy process, from understanding local conditions and inequities, to framing and building support for issues and policy solutions, to monitoring progress toward equity results. Neighborhood-level data that can be mapped and layered is also valuable for revealing the relationships between different issues such as financial security and displacement, community assets and potential development and market opportunities, as well as the cumulative effects of varied risks, harms, or barriers. Disaggregated data and community mapping can also illuminate the experiences of marginalized people and communities to decision makers, and shed light on issues made purposefully invisible. 

But while we live in the age of data, the right data and the tools for analyzing, displaying, and sharing it are often elusive for underresourced community groups. 

Over the past decade, community leaders and a growing array of institutions have begun building new data tools with the explicit purpose of addressing this mismatch and advancing equity. In 2007, Portland, Oregon’s Coalition for a Livable Future launched the nation’s first “regional equity atlas,” a printed volume of maps documenting the vast disparities in access to resources and opportunities across the region and supporting successful advocacy to target investments to communities of color and low-income communities. Other communities—Atlanta, Denver, and Los Angeles—followed suit and created their own atlases, mapping a multitude of indicators across the various domains that influence health, from employment to transportation to housing to community safety and more. 

At the national level, more data tools for equity have emerged. Some comprehensively depict equity conditions for multiple communities, such as the National Equity Atlas and diversitydatakids.org. Others provide disaggregated community data for specific issues and policy areas, such as Mapping Police Violence (community safety and justice) or Clocking-In (wages and workers’ rights).

See the full report from PolicyLink and Ecotrust.

Filed Under: News

October is National Medicine Abuse Awareness Month: CADCA Provides Prevention Resources

October 6, 2017

October is National Medicine Abuse Awarness Month (NMAAM).  Community Anti-Drug Coalitions of America (CADCA) and Prevent MedAbuse offers an Online Rx Abuse Prevention Toolkit on that contains facts, strategies and tools to prevent and reduce teen Rx medicine abuse in your community. This newly revised toolkit is based on CADCA’s Seven Strategies for Effective Community Change. Incorporating these strategies will help you formulate, modify and implement your prevention and intervention strategies.

How to Use the Toolkit:

  • Prevention Strategies: See the Seven Strategies for Effective Community Change in action.
  • Facts & Tools: Review the latest facts on this drug abuse challenge. Discover how to conduct an Rx abuse community assessment. Check out the Sample Logic Model. See how this information gets translated into Sample Intervention Maps.
  • Other Resources: Learn about information and tools that can make your programs and interventions successful, including share tools that you can place on your website, Facebook or e-mail signature blocks.
  • Success Stories: View Rx prevention at work. Check out the video presentations from CADCA coalitions nationwide that are experiencing Rx medication prevention success.

You can also get involved in Medicine Abuse Awareness Month by joining CADCA’s campaign:

  • Register for the Dose of Prevention Challenge: Join community organizations and individuals around the country to spur discussions in your community to find solutions to this complex problem.
  • Grassroots Media Kit: Amplify your medicine abuse prevention messages using CADCA’s Grassroots Media Kit. This Kit provides several tools to help you plan and promote your National Medicine Abuse Awareness Month activities.
  • Share Tools: Download graphics and banners to spread the word about National Medicine Abuse Awareness Month this October.

Helpful Materials you can Download:

  • Fact Sheets, Presentations, and Brochures about medicine abuse
  • Preventing Teen Cough Medicine Abuse: A Parent’s Guide
  • Checklist to help plan a town hall meeting
  • “Stopping Cough Medicine Abuse in your Community” video to show at an event

“Prescription drug abuse is an epidemic that requires more than one strategy or tactic. It’s going to take a comprehensive approach that employs multiple strategies to create population-level reductions to this problem,” notes General Arthur Dean, the Chairman and CEO of CADCA. 

View the Toolkit at PreventMedAbuse.org or see more about CADCA’s NMAAM campaign.

Filed Under: News

NIH to Fund Seven Research Centers in Minority Institutions

October 5, 2017

The National Institute on Minority Health and Health Disparities (NIMHD), part of the National Institutes of Health, will fund seven new awards to support the Research Centers in Minority Institutions (RCMI) Specialized Centers program. RCMI is designed to support institutional research capacity and foster the career development of new and early career investigators conducting minority health and health disparities research. The centers will share approximately $122 million over five years, pending available funds.

The primary goals of the RCMI specialized centers are: to enhance institutional research capacity within the areas of basic biomedical, behavioral, and/or clinical research; enable investigators of all levels to become more successful in obtaining competitive extramural support, especially from NIH, particularly on diseases that disproportionately affect minority and other health disparity populations; foster environments conducive to career enhancement, with a special emphasis on development of new and early career investigators; enhance the quality of all scientific inquiry and promote research on minority health and health disparities; and establish sustainable relationships with community-based organizations that will partner with the RCMI institution.

“Institutions with historical commitment to diversity are essential to supporting scientific research and providing health care to underserved communities,” said NIMHD Director Dr. Eliseo J. Pérez-Stable. “These institutions are uniquely positioned to engage minority populations in research, and in the translation of research advances into culturally competent, measurable and sustained improvements in health outcomes.”

The seven RCMI grantees are:

1. Center for Reducing Health Disparities in Substance Abuse and HIV in South Florida

Eric F. Wagner, Ph.D.  |  Florida International University, Miami

The center will partner with communities in the Miami Dade region, which has a high prevalence of substance use and some of the highest HIV incidences in the country, particularly among underrepresented minorities, to develop a sustainable national clinical and behavioral research training program that addresses health inequities and disparities associated with these health problems.

2. RCMI Program in Health Disparities Research

Maria F. Lima, Ph.D. and James E. K. Hildreth, M.D., Ph.D.  |  Meharry Medical College, Nashville, Tennessee

The program will support four research projects addressing HIV/AIDS, prostate cancer, racial and ethnic differences in periodontal disease microbiomes, and adversity-driven chronic pain to advance fundamental understanding of these health disparities.

3. RCMI Center for Health Disparities Research

Deepak Kumar, Ph.D.  |  North Carolina Central University, Durham

The center will conduct three innovative basic biomedical and behavioral research projects, along with health disparities research pilot projects with robust mentoring, leveraging resources and partnerships at community-based organizations and neighboring institutions in the Research Triangle area. The center will also promote a collaborative research environment conducive to career enhancement for postdoctoral trainees and NCCU faculty at all levels.

4. Southwest Health Equity Research Collaborative (SHERC)

Julie A. Baldwin, Ph.D.  |  Northern Arizona University, Flagstaff

The center will increase research capacity in environmental and community health to address health disparities among diverse populations of the southwestern United States. Research projects will explore environmental factors and conditions that might lead to increased risk for health issues and disease transmission, as well as biological variables that may affect disease mortality in the underserved. Through community collaborations, SHERC will identify relevant strategies to enhance community assets and resilience to minimize the impacts of health disparities in the region.

5. Center for Biomedical Research/Research Centers at Minority Institutions

Clayton Yates, Ph.D.  |  Tuskegee University, Alabama

The center will enhance its research infrastructure and increase the numbers and proficiency of minority scientists engaged in advanced biomedical research focused on health disparities, including those for HIV, obesity, and prostate cancer, all of which disproportionately affect underrepresented minorities, especially African Americans residing in the “Black Belt” counties of Alabama. The center will also engage local communities to better understand and address health issues that affect them.

6. Ola HAWAII

Jerris R. Hedges, M.D.  |  University of Hawaii at Manoa

The project is designed to advance “ola” (health in Hawaiian) for communities experiencing genetic, environmental, and socioeconomic disparities in health. The center will foster high-impact, team-science research addressing health disparities; strengthen and diversify the basic biomedical, behavioral and clinical research workforce and thinkforce focusing on health disparities; and enhance, consolidate and sustain core facilities and resources for health disparities research.

7. Center for Collaborative Research in Minority Health and Health Disparities

Emma Fernández-Repollet, Ph.D.  |  University of Puerto Rico Medical Sciences Campus, San Juan

The center will support translational research projects in basic biomedical, behavioral, and clinical research that will provide different and innovative approaches to promoting minority health and health disparities research among early career investigators and students, enhancing participation of Hispanic patients in genomics studies, and providing novel interventions to reduce childhood obesity within and outside Puerto Rico.

Learn more at NIH.gov.

Filed Under: News

  • « Go to Previous Page
  • Go to page 1
  • Interim pages omitted …
  • Go to page 144
  • Go to page 145
  • Go to page 146
  • Go to page 147
  • Go to page 148
  • Interim pages omitted …
  • Go to page 171
  • Go to Next Page »

Footer

Facebook Logo
Linkedin Logo
Twitter Logo
The NNED has been a multi-agency funded effort with primary funding by the Substance Abuse and Mental Health Services Administration (SAMHSA). It is managed by SAMHSA and the Achieving Behavioral Health Excellence (ABHE) Initiative.
  • About
  • Contact
  • Privacy Policy