Eating Disorders
Moreno, R., Buckelew, S.M., Accurso, E.C. et al. Disparities in access to eating disorders treatment for publicly-insured youth and youth of color: a retrospective cohort study. J Eat Disord 11, 10 (2023). https://doi.org/10.1186/s40337-022-00730-7
,Pascal Beckert-McGirr, B.A. (he/him/his)
Clinical Research Assistant
Children’s Hospital of Philadelphia
philadelphia, Pennsylvania, United States
Carolyn Becker, Ph.D. (she/her/hers)
Professor
Trinity University
San Antonio, Texas, United States
Blair Burnette, Ph.D. (she/her/hers)
Michigan State University
East Lansing, Michigan, United States
Lisa Kilpela, Ph.D. (she/her/hers)
Assistant professor
UT Health San Antonio
San Antonio, Texas, United States
Maria Kalantzis, B.S., M.A. (she/her/hers)
PhD Candidate
Bowling Green State University
Bowling Green, Ohio, United States, Ohio, United States
Jacqueline Kosmas, M.A. (she/her/hers)
Virginia Polytechnic Institute and State University
Blacksburg, Virginia, United States
Pascal Beckert-McGirr, B.A. (he/him/his)
Clinical Research Assistant
Children’s Hospital of Philadelphia
philadelphia, Pennsylvania, United States
Eating disorders (EDs) are a group of complex biobehavioral disorders that often onset during adolescence but can persist until or emerge later in life. Intervening early in the illness course is paramount, as EDs have a high mortality rate and evidence suggests improved outcomes with prompt treatment. Specifically, delayed access to ED care is associated with a more chronic and persistent course of illness and can have devastating psychological and physiological complications including severe malnutrition, organ failure, and death. Thus, removing barriers to accessing ED care is crucial to improving outcomes for individuals with an ED.
Widespread misconceptions portray those with an ED as thin, White, affluent, cisgender females, but these assumptions are not supported by evidence. Indeed, fewer than 6% of those with an ED are ever clinically underweight, and those with lower socioeconomic status are 27% more likely to screen positive for an ED than their higher socioeconomic status counterparts. Those with marginalized racial, ethnic, sexual, and gender identities are also at risk for EDs at similar or greater rates to their non-marginalized counterparts. Despite this, individuals with an ED who hold one or more marginalized identities are less likely to be screened for an ED, be referred to care, or receive treatment for their ED.
These misconceptions have contributed to a paucity of research examining EDs in those living in poverty, in higher weight bodies, and with marginalized racial and ethnic identities. Thus, significant gaps exist in determining the efficacy of treatments in diverse populations, as well as the dissemination of effective, accessible treatments to everyone who may suffer from or be at risk of an ED. To ensure equity in ED care, we must identify and address barriers to accessing care for all with an ED and ensure our research is conducted in representative samples to maximize generalizability.
This symposium will examine current research on barriers to accessing ED treatment and proposed solutions to increase access. Our speakers will discuss racial inequities in ED research, current disparities in treatment, and a novel, community developed single-session intervention to increase access to ED treatment. Rather than simply focusing on existing barriers/problems within the current system, we will take a solution-focused approach to identify opportunities for improvements in care and, alongside the conference theme, will inspire innovative ways for providers and researchers to be inclusive of historically marginalized individuals. Presentations will emphasize the role of advocacy in developing effective solutions to overcome barriers to treatment for groups historically underrepresented in ED treatment and research.
Speaker: Blair Burnette, Ph.D. (she/her/hers) – Michigan State University
Co-author: Cecelia Tucker, BA – Michigan State University
Co-author: Emma K. Crumby, BS – University of Louisville
Co-author: Heather A. Davis, Ph.D. (she/her/hers) – Virginia Polytechnic Institute and State University
Speaker: Lisa Kilpela, Ph.D. (she/her/hers) – UT Health San Antonio
Co-author: Enya Vroom, Ph.D. (she/her/hers) – UT Health San Antonio
Co-author: Salome Wilfred, MA – UNC
Co-author: Savannah C. Hooper, B.A. – The University of Louisville
Co-author: Victoria B. Marshall, B.A. – University of Texas Health Science Center at San Antonio
Speaker: Maria A. Kalantzis, B.S., M.A. (she/her/hers) – Bowling Green State University
Co-author: Abby Braden, Ph.D. – Bowling Green State University
Speaker: Jacqueline A. Kosmas, M.A. (she/her/hers) – Virginia Polytechnic Institute and State University
Co-author: Anna Gabrielle G. Patarinski, B.S. – Virginia Polytechnic Institute and State University
Co-author: Kendall B. Holloway, M.S.Ed, LPC – Virginia Polytechnic Institute and State University
Co-author: Heather A. Davis, Ph.D. (she/her/hers) – Virginia Polytechnic Institute and State University
Speaker: Pascal Beckert-McGirr, B.A. (he/him/his) – Children’s Hospital of Philadelphia
Co-author: Samantha Turner, Ph.D., RN – Children’s Hospital of Philadelphia
Co-author: William A. Brake, B.A. – The Children’s Hospital of Philadelphia
Co-author: Grace Haase, B.A. (she/her/hers) – Children's Hospital of Philadelphia
Co-author: Marita Cooper, Ph.D. (she/her/hers) – Children’s Hospital of Philadelphia
Co-author: C.Alix Timko, PhD – Children's Hospital of Philadelphia