From Screening to Support: A Multi-Method Analysis of HRSN Integration in Cancer Care
2 other identifiers
observational
500
1 country
1
Brief Summary
This observational study aims to identify the factors that influence whether cancer patients accept or decline supportive care services after screening positive for health-related social needs (HRSNs) at the Sidney Kimmel Comprehensive Cancer Center. The study focuses on adult oncology patients who previously reported at least one HRSN-such as transportation, food, housing, or utility needs-but declined assistance when it was offered. The main questions it aims to answer are:
- What factors shape cancer patients' intentions to use supportive care services for HRSNs?
- Why do patients who screen positive for HRSNs choose not to accept help offered by the healthcare system? Participants will:
- Complete a one-time electronic survey delivered via MyChart or email.
- Optionally participate in a semi-structured Zoom interview (for a subset of 20-30 survey respondents) to explore decision-making in greater depth.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 11, 2025
CompletedFirst Submitted
Initial submission to the registry
January 9, 2026
CompletedFirst Posted
Study publicly available on registry
January 20, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 1, 2027
February 12, 2026
February 1, 2026
1.1 years
January 9, 2026
February 10, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Factors influencing cancer patients' intent to use oncology supportive care for HRSNs
Measured via Surveys (self-reported) using a structured questionnaires with binary (Yes/No) responses and Likert Style questions (Quality of Life and FACT-ES).
approximately 4 months
Secondary Outcomes (1)
Factors associated with declining HSRN-related supportive care services
approximately 4 months
Study Arms (1)
Cancer Patients Screened for Health-Related Social Needs (HRSNs)
This group includes adult cancer patients receiving care at Sidney Kimmel Comprehensive Cancer Center (SKCCC) who previously completed a Health-Related Social Needs (HRSNs) screening in the electronic health record. This will be achieved by providing patients with a one-time survey. The surveys will be distributed via MyChart messages and emails. Additionally, 20 patients who complete the survey will be asked to complete a short interview to further understand why cancer patients identified as high-risk for HRSNs decline connections to care and intervention-ultimately to gain an understanding into the factors that they take into account when determining whether they want to be connected to a resource or service connection related to HRSNs.
Interventions
Participants complete a one-time electronic survey to assess factors influencing the decision to decline assistance for identified Health-Related Social Needs (HRSNs). The survey includes questions related to transportation access, food insecurity, housing instability, and utility needs. Survey completion takes approximately 10 minutes.
Interviews will be semi-structured and will be offered to 20 participants who have completed the survey and meet eligibility criteria. Interviews will be conducted via a Zoom. Zoom will create a transcription of the interview which will be saved in a secure encrypted space, no video will be saved.
Eligibility Criteria
Adult cancer patients who received care at SKCCC who were engaged in HRSN screening
You may qualify if:
- Provide informed consent via check box for survey
- Provide verbal consent via Zoom for interview
- Must be able to read and understand English
- Willing to comply with all study procedures and be available for the duration of the study
- Patients with existing HRSN data in their EHR that answere4d yes to risk in at least one domain and no to wanting help/follow up
You may not qualify if:
- An individual who meets any of the following criteria will be excluded from participation in this study:
- If they do not consent
- Non-patients with existing HRSN data in their EHR
- Individuals unable to complete the survey due to language barriers or other cognitive limitations
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sidney Kimmel Cancer Center at Thomas Jefferson University
Philadelphia, Pennsylvania, 19107, United States
MeSH Terms
Conditions
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Munjireen Sifat, PhD, MPH
Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 9, 2026
First Posted
January 20, 2026
Study Start
December 11, 2025
Primary Completion (Estimated)
January 1, 2027
Study Completion (Estimated)
January 1, 2027
Last Updated
February 12, 2026
Record last verified: 2026-02