Actively Recruiting
PROACT is a Prospective Master Protocol for a Cohort Study Focused on Evaluating the Implementation of Integrated Proactive Supportive Care Pathways at Gustave Roussy
Led by Gustave Roussy, Cancer Campus, Grand Paris · Updated on 2026-01-16
700
Participants Needed
1
Research Sites
181 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
PROACT is a prospective master protocol for a cohort study focused on evaluating the implementation of integrated proactive pathways of supportive care. This is an observational cohort study in the context of a quality-of-care initiative. It will be evaluated by its impact on patient's distress measured by the NCCN's Distress thermometer at 12 weeks after entering the pathway.
CONDITIONS
Official Title
PROACT is a Prospective Master Protocol for a Cohort Study Focused on Evaluating the Implementation of Integrated Proactive Supportive Care Pathways at Gustave Roussy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Histological confirmation of cancer (any cancer type, any stage)
- Age 18 years or older
- Received an integrated supportive care needs assessment
- Signed consent form for the PROACT study
You will not qualify if you...
- Absence or inability to provide written consent
- Inability to understand or speak French
AI-Screening
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Trial Site Locations
Total: 1 location
1
Gustave Roussy
Villejuif, France, 94800
Actively Recruiting
Research Team
M
Maria Alice BORINELLI-FRANZOI
CONTACT
A
Aude BARBIER
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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