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University of Washington · Theatre
Active 2006–2026
Marcela A. Fuentes is an associate professor in the Performance Studies Department at Northwestern University’s School of Communication. Her work studies the role that performance plays in collective action towards social justice, analyzing symbolic, embodied, and time-based modes of communication and intervention in street protests, social media activism, and participatory art from the mid-nineties to the present. She focuses on emerging modalities of aesthetic expression, civic engagement, and transnational mobilization, particularly within trans-feminist struggles. Her research tracks how notions central to performance studies such as embodiment, liveness, eventness, and site-specificity are redefined in the era of digitally mediated communication. Her latest book, Performance Constellations: Networks of Protest and Activism in Latin America, maps the entanglement of street protests and digitally mediated mobilizations in response to state violence and neoliberal exploitation, including a chapter on transnational feminist mobilizations. She has been awarded national and international fellowships and grants, including the Fulbright Fellowship and the Andrew W. Mellon postdoctoral research grant. Her work has been published in various academic journals and edited volumes, and her research interests include feminist theory and performance, theories of embodiment, affect theory, queer of color critique, hemispheric performance, practice-based research, and digital humanities. She has also served as an external consultant for the Buenos Aires Performance Biennial and as a council member of the Hemispheric Institute of Performance and Politics. Her lecture performances have been presented in Argentina, Brazil, and the US.
Preferences for Chronic Pain Treatment Among Indigenous Peoples Living in the Pacific Northwest
International Journal of Environmental Research and Public Health · 2026-04-14
There is a significant need for culturally appropriate psychological treatments for chronic pain among American Indian/Alaska Native (AI/AN) peoples. This study used Indigenous community-based participatory research methods with the Portland Area Indian Health Services-Yakama Service Unit (YSU) to gather information needed for developing culturally adapted psychological treatments for AI/AN individuals with chronic pain. This study included remote semi-structured focus groups with 16 AI/AN individuals with chronic pain to identify pain treatment preferences (Aim 1) and priorities for pain treatment outcome domains (Aim 2). Thematic analyses were conducted with Atlas.ti (version 23.2.1). Results indicated a high interest in psychological interventions and concern that referral to psychological treatment meant that pain is "not real." Pain intensity and pain interference were identified as the most important outcome domains. To measure pain intensity, the 0 to 10 Numerical Rating Scale was most preferred. The findings support the potential utility of culturally adapted psychological treatments for chronic pain for AI/AN individuals and provided information regarding the adaptations that would be most useful.
Frederick P. Rivara
Seattle Children's Hospital
Nathalia Jimenez
University of Washington
Susan Apkon
University of Colorado Denver
Chuan Zhou
University of Washington
Deborah Crawley
Harborview Injury Prevention and Research Center
MS, Health Services
University of Washington
MD
University of Michigan Medical School
B.S.
Stanford University
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Prescribing Justice: How Pediatric Physiatrists Can Close the Disability Equity Gap
Current Physical Medicine and Rehabilitation Reports · 2025-10-17
A pediatric rehabilitation therapy audit study: A brief report
Journal of Pediatric Rehabilitation Medicine · 2025-05-15
PurposeChildren with disabilities benefit from physical, occupational, and speech therapy, but families identify unmet needs for these services. The purpose of this study was to audit access to therapy services in a tri-state region. It was hypothesized that children who were publicly insured and children from minoritized identity groups would face greater access barriers and longer wait times than children covered by private insurance and non-minoritized White children.MethodsThis prospective audit study utilized callers who posed as mothers seeking outpatient therapy services for their child. Access difficulties were identified based on the number of phone calls required to obtain an appointment or determine if services would be obtained at all, as well as the number of days to the earliest available appointment.ResultsTherapy appointment access was a problem for 47.4% of simulated families. After 251 phone calls, 91 simulated families were able to schedule appointments in 76 clinics. Black and Hispanic simulated families had a harder time getting appointments, but days to appointment did not differ by telegraphed minoritized identity (F(3,88) = 1.474, p = .227).ConclusionSimulated families experienced substantial barriers to arranging therapy appointments with Black and Hispanic families experiencing more barriers than their White and Muslim peers.
Preferences for Chronic Pain Treatment Among American Indian and Alaska Natives
Journal of Pain · 2024-04-01
Health Equity · 2024-04-01
Background: Limited availability and poor quality of data in medical records and trauma registries impede progress to achieve injury-related health equity across the lifespan. Methods: We used a Nominal Group Technique (NGT) in-person workgroup and a national web-based Delphi process to identify common data elements (CDE) that should be collected. Results: The 12 participants in the NGT workgroup and 23 participants in the national Delphi process identified 10 equity-related CDE and guiding lessons for research on collection of these data. Conclusions: These high-priority CDE define a detailed, equity-oriented approach to guide research to achieve injury-related health equity across the lifespan.
Value in Health · 2024-12-01
Neurorehabilitation · 2023-04-25 · 4 citations
BACKGROUND: Return to school is key for community re-integration after a traumatic brain injury (TBI). School support facilitates and ensure a successful transition back to school. However, access to school services is not uniform among U.S. children. OBJECTIVE: To describe school services for children with TBI from minoritized backgrounds and highlight population-specific risk factors and facilitators for accessing services. METHODS: Narrative review of the literature including studies on return to school after a mild-complicated, moderate, or severe TBI, among children enrolled in the U.S. school system. We describe receipt of services, enabling and risk factors, and outcomes, for minority children. RESULTS: There is a gap in knowledge regarding return to school among minoritized children with TBIs. Studies have few participants from racial and ethnic minority backgrounds, or low income or rural communities. Transgender and non-binary youth are not represented in present research efforts. Studies highlight larger barriers to receipt of school services among minority children and additional barriers associated with their minority status. CONCLUSION: Diversity in the U.S pediatric population is increasing. Minoritized populations are at increased risk for TBI and poor outcomes. Research focused on the needs of these populations is required to optimize school return after TBI hospitalization and overall post-discharge care.
PM&R · 2023-01-19 · 3 citations
Person-and caregiver-centered care. Qualitative study in an elderly patient with cancer
Journal of Geriatric Oncology · 2023-11-01
Archives of Physical Medicine and Rehabilitation · 2023-04-17
OBJECTIVE: Provide proof-of-concept for development of a Pediatric Functional Status eScore (PFSeS). Demonstrate that expert clinicians rank billing codes as relevant to patient functional status and identify the domains that codes inform in a way that reliably matches analytical modeling. DESIGN: Retrospective chart review, modified Delphi, and nominal group techniques. SETTING: Large, urban, quaternary care children's hospital in the Midwestern United States. PARTICIPANTS: Data from 1955 unique patients and 2029 hospital admissions (2000-2020); 12 expert consultants representing the continuum of rehabilitation care reviewed 2893 codes (procedural, diagnostic, pharmaceutical, durable medical equipment). MAIN OUTCOME MEASURES: Consensus voting to determine whether codes were associated with functional status at discharge and, if so, what domains they informed (self-care, mobility, cognition/ communication). RESULTS: The top 250 and 500 codes identified by statistical modeling were mostly composed of codes selected by the consultant panel (78%-80% of the top 250 and 71%-78% of the top 500). The results provide evidence that clinical experts' selection of functionally meaningful codes corresponds with codes selected by statistical modeling as most strongly associated with WeeFIM domain scores. The top 5 codes most strongly related to functional independence ratings from a domain-specific assessment indicate clinically sensible relationships, further supporting the use of billing data in modeling to create a PFSeS. CONCLUSIONS: Development of a PFSeS that is predicated on billing data would improve researchers' ability to assess the functional status of children who receive inpatient rehabilitation care for a neurologic injury or illness. An expert clinician panel, representing the spectrum of medical and rehabilitative care, indicated that proposed statistical modeling identifies relevant codes mapped to 3 important domains: self-care, mobility, and cognition/communication.
Edgar Torres López
University of Illinois Chicago
Alyssa Virtue
Harborview Injury Prevention and Research Center
Laura Alonso-Gonzalez
Center for Children