Actively Recruiting
Spanish Validation of a Psychosocial Needs Assessment for Adolescents and Young Adults With Cancer (AYA-POST)
Led by Hospital Universitari Vall d'Hebron Research Institute · Updated on 2026-01-21
100
Participants Needed
1
Research Sites
368 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This prospective multicenter study aims to validate the Spanish version of the Distress Thermometer and accompanying list of psychosocial needs specifically adapted for adolescents and young adults (AYA) aged 15 to 25 who are diagnosed with cancer. These tools, firstly developed by the National Comprehensive Cancer Network (NCCN) and then specifically adapted for AYA by Canteen Australia and validated in English-speaking countries, are widely used around the world to quickly identify emotional distress and unmet practical or social needs in cancer patients, helpting to detect their emotional distress and support needs, which can differ significantly from those of children or older adults. By validating these screening tools in Spanish this study seeks to confirm whether they can reliably identify young patients who may be experiencing psychosocial difficulties. Once validated, these tools can be easily integrated into clinical practice in Spanish-speaking countries, helping healthcare teams quickly identify vulnerable young patients, respond to their emotional needs earlier, and improve the overall quality of care. The results will also highlight which psychosocial needs are most common in AYA cancer patients, supporting the development of future programs and services tailored to this population.
CONDITIONS
Official Title
Spanish Validation of a Psychosocial Needs Assessment for Adolescents and Young Adults With Cancer (AYA-POST)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients between 15 and 25 years old who provide informed consent (over 18 years old) or parents provide consent and patient consents if minors (15 to 18 years old)
- Diagnosis of cancer (malignant solid tumor or hematologic malignancy) within 6 months prior to study inclusion or first non-surgical treatment started within last 6 months
- Treated from diagnosis or first non-surgical treatment at participating study centers
You will not qualify if you...
- Patients not receiving their first line of non-surgical treatment
- Patients who do not have a good understanding of Spanish
- Patients with severe neurological impairment or other conditions preventing proper completion of study procedures
AI-Screening
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Trial Site Locations
Total: 1 location
1
Hospital Vall Hebron
Barcelona, Barcelona, Spain, 08035
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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