NCT07484282

Quality of Care for Adolescent and Young Adult (AYA) Patients Living With Serious or Advanced Cancer

• Status: Withdrawn
• Phase: —
• Study type: Observational
• Enrollment: 0 (actual)
• Sponsor: National Cancer Institute (NCI) · NIH
• Sex: All
• Age: 12 Years – 120 Years
• Healthy volunteers: Not accepted

Summary

Background: Cancer among adolescents and young adults (AYAs) is on the rise, with nearly 90,000 AYAs diagnosed in the US each year. While most are cured, an estimated 15,000 AYAs die of cancer in the US annually creating profound suffering for those whose lives are cut short and for those who survive them. AYAs face unique challenges near the end of life (EOL). The tragic circumstances surrounding young lives cut short by cancer often provoke intensive efforts to prolong life, sometimes at the cost of comfort and quality. Patients, families, and even clinicians experience these deaths as tragic, a departure from the natural order of life in which each generation outlives the one before it. The current study is designed to ensure future efforts to improve care is guided by patient perspectives. The aims of the study are to 1) measure the quality of care received by adolescents and young adults (AYAs) living with advanced cancer using patient-centered quality measures, focusing specifically on potential unmet psychosocial, spiritual, and communication needs and 2) to assess disparities in end-of-life (EOL) care quality and barriers to care experienced by Black, Asian, and Hispanic AYAs. Our research will enable us to answer remaining critically unanswered questions and unmet needs about EOL care quality and barriers to care experienced by AYAs.

Detailed description

Objectives: * Aim 1: To measure the quality of care received by adolescents and young adults (AYAs) living with advanced cancer using patient-centered quality measures. * Hypothesis 1.1: AYAs experience high unmet need for psychosocial and spiritual care and communication. * Hypothesis 1.2: Unmet needs for care of physical and psychosocial symptoms intensify over time. * Aim 2: To assess disparities in end-of-life (EOL) care quality and barriers to care experienced by Black, Asian, and Hispanic AYAs. * Hypothesis 2.1: Black, Asian, and Hispanic AYAs are at risk for inferior quality care relative to White patients, with areas of greatest disparity in attention to physical symptoms and communication. * Hypothesis 2.2: Black, Asian, and Hispanic AYAs experience unique barriers to high-quality EOL care, including structural, interpersonal, and individual factors, as well as culturally informed influences.

Conditions

• Cancer
• Patients Living With Stage IV or Recurrent Cancer

Interventions

Type	Name	Description
OTHER	Quality Assessment	Participation in surveys, interviews and/or panels.

Timeline

• Start date: 2026-04-07
• Primary completion: 2029-04-01
• Completion: 2029-04-01
• First posted: 2026-03-20
• Last updated: 2026-04-03

Locations

1 site across 1 country: United States