Other Titles

Rising Star Poster/Presentation

Abstract

Background: Cancer is the leading cause of death among Hispanic people, accounting for 20% of deaths (American Cancer Society, 2023). In 2024, the American Cancer Society predicted that 195,300 Hispanics would be diagnosed with cancer in the United States, and 50,400 (25%) would die from their disease, leaving approximately 144,900 (75%) living with cancer. As the Hispanic population rises in the United States, one can predict that cancer diagnoses will also increase. This is likely to result in a higher number of cancer-related deaths, as well as more individuals living with cancer. Consequently, there will be an increased demand for palliative care services. This highlights the importance of educating and training healthcare providers to properly care for the increased number of Hispanic individuals with cancer who will benefit from palliative care.

Purpose: To explore the knowledge and perceptions of Hispanic individuals with cancer and their caregivers about palliative care post-consultation or follow up.

Specific Aims: 1. To examine palliative care perceptions of Hispanic individuals with cancer and their caregivers; 2. To explore the dynamics between Hispanic individuals with cancer and their caregivers when discussing palliative care in Spanish and their perspectives; and 3. To examine the role of language in the understanding and acceptance of palliative care for Hispanic people with cancer and their caregivers.

Methods: Focused ethnography approach: First-time palliative care consultation or follow up and post-consultation or follow up semi-structured dyadic interviews of inpatient or outpatient Hispanic and Spanish-speaking adult oncology patients and their primary caregiver from an academic medical center in the Bronx, NY. This will be done until data saturation is reached, which will determine the sample size.

Data to be collected: Demographic characteristics. Data analysis will begin with the first interview and continue until data saturation is reached. I will use NVivo to organize, visualize, and analyze the data. The following systematic approach for analyzing the data will be utilized:

1. coding the data,

2. grouping patterns,

3. identifying outliers,

4. generalizing themes and sub/themes, and

5. reflective remarks.

An additional approach in the data analysis process that will be implemented to ensure credibility and validity will be to have my chair, a qualitative expert, and a Spanish-speaking committee member review my themes and subthemes.

Notes

Extensive reference list included as separate file.

Description

Cancer remains the leading cause of death among Hispanic individuals in the U.S., and rising population trends are expected to increase diagnoses and palliative care needs. This study explores Hispanic cancer patients’ and caregivers’ knowledge and perceptions of palliative care after consultation using focused ethnography. Semi structured dyadic interviews will be conducted until data saturation, with NVivo used for systematic qualitative analysis.

Author Details

Carla McNulty MSN, FNP-BC, BSN, RN, OCN, PhD student;

Catherine Finlayson, PhD, RN, OCN, Dissertation Chair

Pace University Lienhard School of Nursing

Sigma Membership

Delta Zeta, Omega Delta

Type

Poster

Format Type

Text-based Document

Study Design/Type

Ethnography

Research Approach

Qualitative Research

Keywords:

Palliative Care, Hispanic Americans, Cancer Patients, Communication, Communication Barriers, Health Knowledge--Evaluation

Conference Name

37th International Nursing Research Congress

Conference Host

Sigma Theta Tau International

Conference Location

Toronto, Ontario, Canada

Conference Year

2026

Rights Holder

All rights reserved by the author(s) and/or publisher(s) listed in this item record unless relinquished in whole or part by a rights notation or a Creative Commons License present in this item record. All permission requests should be directed accordingly and not to the Sigma Repository. All submitting authors or publishers have affirmed that when using material in their work where they do not own copyright, they have obtained permission of the copyright holder prior to submission and the rights holder has been acknowledged as necessary.

Review Type

Invited Presentation

Acquisition

Proxy-submission

Date of Issue

2026-10-01

Click on the above link to access the poster.

Additional Files

References.pdf (132 kB)

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Rompiendo Fronteras: Addressing Language Barriers in Hispanic Palliative Cancer Care

Toronto, Ontario, Canada

Background: Cancer is the leading cause of death among Hispanic people, accounting for 20% of deaths (American Cancer Society, 2023). In 2024, the American Cancer Society predicted that 195,300 Hispanics would be diagnosed with cancer in the United States, and 50,400 (25%) would die from their disease, leaving approximately 144,900 (75%) living with cancer. As the Hispanic population rises in the United States, one can predict that cancer diagnoses will also increase. This is likely to result in a higher number of cancer-related deaths, as well as more individuals living with cancer. Consequently, there will be an increased demand for palliative care services. This highlights the importance of educating and training healthcare providers to properly care for the increased number of Hispanic individuals with cancer who will benefit from palliative care.

Purpose: To explore the knowledge and perceptions of Hispanic individuals with cancer and their caregivers about palliative care post-consultation or follow up.

Specific Aims: 1. To examine palliative care perceptions of Hispanic individuals with cancer and their caregivers; 2. To explore the dynamics between Hispanic individuals with cancer and their caregivers when discussing palliative care in Spanish and their perspectives; and 3. To examine the role of language in the understanding and acceptance of palliative care for Hispanic people with cancer and their caregivers.

Methods: Focused ethnography approach: First-time palliative care consultation or follow up and post-consultation or follow up semi-structured dyadic interviews of inpatient or outpatient Hispanic and Spanish-speaking adult oncology patients and their primary caregiver from an academic medical center in the Bronx, NY. This will be done until data saturation is reached, which will determine the sample size.

Data to be collected: Demographic characteristics. Data analysis will begin with the first interview and continue until data saturation is reached. I will use NVivo to organize, visualize, and analyze the data. The following systematic approach for analyzing the data will be utilized:

1. coding the data,

2. grouping patterns,

3. identifying outliers,

4. generalizing themes and sub/themes, and

5. reflective remarks.

An additional approach in the data analysis process that will be implemented to ensure credibility and validity will be to have my chair, a qualitative expert, and a Spanish-speaking committee member review my themes and subthemes.