Actively Recruiting
The PRISM-Social Needs (PRISM-SN) Intervention for Adolescents and Young Adults With Cancer
Led by Seattle Children's Hospital · Updated on 2024-06-25
100
Participants Needed
1
Research Sites
115 weeks
Total Duration
On this page
Sponsors
S
Seattle Children's Hospital
Lead Sponsor
U
University of Pittsburgh Medical Center
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this study is to establish feasibility, acceptability, and proof-of-concept of an psychosocial intervention adapted to address social health needs of adolescents and young adults (AYAs) newly diagnosed with cancer. The aims of this study are to: 1. Determine if the Promoting Resilience in Stress Management - Social Needs (PRISM-SN) adapted intervention is feasible and acceptable, defined via program uptake and retention and patient-reported feedback. 2. Explore whether PRISM-SN improves social outcomes at 12-week follow-up compared to usual care. Participants will be randomized to receive usual psychosocial care or the PRISM-SN program. Participants on both arms will complete patient-reported outcome surveys at enrollment and 12-weeks later. Researchers will compare participants who received the PRISM-SN program to those who received usual care to see if the program improves psychosocial outcomes.
CONDITIONS
Official Title
The PRISM-Social Needs (PRISM-SN) Intervention for Adolescents and Young Adults With Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 12-25 years
- Diagnosed with new malignancy treated with chemotherapy and/or radiation less than 6 months ago
- Able to speak in the English language
- Able to read in the English language
- Cognitively able to participate in intervention sessions and complete surveys
You will not qualify if you...
- Aged under 12 or over 25 years
- Diagnosed with recurrent malignancy
- Diagnosed with new malignancy more than 6 months ago
- Not receiving chemotherapy and/or radiation
- Not able to speak in the English language
- Not able to read in the English language
- Not cognitively able to participate in intervention sessions or complete surveys
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Seattle Children's
Seattle, Washington, United States, 98105
Actively Recruiting
Research Team
K
Kaitlyn M Fladeboe, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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