Improving Native American Elder Access to and Use of Healthcare

Overview

This community-driven study features a mixed-method, participatory design to examine help-seeking behavior and healthcare experiences of American Indian elders in New Mexico, in order to develop and evaluate a tailored intervention to enhance knowledge of, access to, and use of insurance and available services to reduce healthcare disparities. This study includes qualitative and quantitative interviews combined with concept mapping and focus groups with American Indian elders and other key stakeholders.

Full Title of Study: “Improving Native American Elder Access to and Use of Healthcare Through Effective Health System Navigation”

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: June 30, 2021

Detailed Description

This five-year project was developed by investigators from the Behavioral Health Research Center of the Southwest (BHRCS), a center of the Pacific Institute of Research and Evaluation (PIRE), the Health Committee of the New Mexico Indian Council on Aging (NMICoA), and the University of New Mexico (UNM). The project combines qualitative and quantitative interviews with concept-mapping (CM) techniques and focus groups to study insurance coverage, help-seeking behavior, and the healthcare experiences of American Indian Elders (AIEs) in New Mexico (NM). Practical knowledge grounded in the actual perspectives of AIEs and other key stakeholders may improve healthcare practices and policies for a population largely excluded from national and state discussions of health reform. The study data will also inform the adaptation and development of culturally tailored programming to enrich understanding and facilitate negotiation of a changing landscape of healthcare by AIEs. Our four specific aims are to: 1. Assess how AIEs understand, access, maintain, and use insurance coverage. 2. Characterize AIE help-seeking and healthcare experiences in dominant service delivery settings, i.e., Indian Health Service (IHS), tribally-run 638 facilities, and managed care programs. 3. Identify and compare factors that affect AIE access to health care as perceived by multiple stakeholders, i.e., AIEs, outreach workers (OWs), healthcare staff and providers, public sector administrators, and tribal leaders. 4. Develop and assess implementation feasibility of a structured intervention for OWs that promotes enhanced patient navigation, in addition to healthcare literacy, access, and usage among AIEs.

Interventions

  • Behavioral: Seasons of Care App
    • A web-based mobile application (app) called the Seasons of Care Elder Navigation Guide will assist elders, their families/caregivers, healthcare providers, outreach workers, and other community members in navigating healthcare and insurance systems. The app has the added advantage of being easy to update to respond to future changes in health care and insurance, and sustainable because it is not dependent on intensive training, developing, and retaining of individuals in professional navigation positions.

Arms, Groups and Cohorts

  • Navigators
    • AIE Navigators will use the Seasons of Care app in the context of their everyday outreach work with AIEs over two four-month intervention periods (P1 and P2). Their goal will be to facilitate health literacy to shift attitudes, beliefs, and behaviors to create a “Culture of Coverage” for AIEs at individual, organizational/community, and policy levels. Separated by distance, the AIE Navigators will receive coaching as necessary, using virtual meeting space, to help refine their implementation skills from a member of the research team with experience in AIE health outreach.
  • American Indian Elders (AIEs)
    • Elders will be exposed to the Seasons of Care app when they reach out to navigators for assistance navigating the healthcare system.
  • Healthcare providers/staff
    • This cohort will be exposed to the Seasons of Care app via navigators and their patients.

Clinical Trial Outcome Measures

Primary Measures

  • User Evaluation Survey
    • Time Frame: Once at the end of P2 (Month 8 of 8)
    • A semi-structured, in-person interview (or focus group, depending on availability) with AIEs and healthcare providers who interacted with a navigator using the Seasons of Care app to assess experiences with, and effects of, the Seasons of Care app; suggestions to improve the Seasons of Care app

Secondary Measures

  • Navigator Pre- and Post-Evaluation Interview
    • Time Frame: Month 1 and 4 (of 8) for P1 Navigators; Month 5 and 8 (of 8) for P2 Navigators
    • A semi-structured, in-person interview comprised of open-ended questions to assess navigator’s confidence and experiences with communicating health information to AIEs and healthcare providers; perceptions of the Seasons of Care app

Participating in This Clinical Trial

Navigators Inclusion Criteria:

  • Working in a health and health insurance outreach – Routinely interacting with AIEs as part of their jobs – Primary service region includes target AIEs. Exclusion Criteria:

  • Not Routinely interacting with AIEs as part of their jobs – Not willing to be trained in or use the Seasons of Care app American Indian Elders (AIEs) Inclusion – Age 55+ – Identifying as AI – Able to read in English – Able to consent and complete study procedures – Interacted with Navigator Exclusion ● Individuals who cannot read in English or who have not interacted with a pilot test Navigator will not be eligible to participate Healthcare Staff/providers Inclusion – Individuals who have been in contact with a pilot test Navigator – Work in a healthcare facility that serves AIEs in one of our 4 regions Exclusion ● Individuals who have not interacted with a pilot test Navigator or do not work in a healthcare facility serving our primary population, will not be eligible to participate

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Pacific Institute for Research and Evaluation
  • Collaborator
    • University of California, San Diego
  • Provider of Information About this Clinical Study
    • Principal Investigator: Cathleen Willging, Senior Research Scientist/Center Director – Pacific Institute for Research and Evaluation
  • Overall Official(s)
    • Cathleen Willging, Principal Investigator, Pacific Institute for Research and Evaluation

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