Clinical trial · Observational
PROACT is a Prospective Master Protocol for a Cohort Study Focused on Evaluating the Implementation of Integrated Proactive Supportive Care Pathways at Gustave Roussy
Integrating PROACTive Care Pathways to Empower and Support Cancer Patients (PROACT)
NCT06479057CI-TRIAL-00101061PROACTrecruitingClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Any Cancer | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Supportive Care Pathway | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- PROACT Supportive Care pathways
- description
- This is a prospective cohort study including patients participating in institutional supportive care pathways at diagnosis, during treatment and after treatment.
- interventionNames
- Other: Supportive Care Pathway
Primary outcomes (2)
- measure
- Patient distress
- timeFrame
- over a 12-week period after the integrated supportive care needs assessment.
- description
- Patient distress collected with NCCN Distress Thermometer
- measure
- Patient unmet needs
- timeFrame
- over a 12-week period after the integrated supportive care needs assessment.
- description
- Patient unmet needs collected with problem list from NCCN Distress thermometer
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Histological confirmation of cancer (any cancer type, any stage) * Age ≥ 18 years old * Received an integrated supportive care need assessment. * Sign the consent form for the PROACT study. Exclusion Criteria: * Absence or inability of written consent from the patient. * Does not understand or speak French.
References
Publications (2)
- DERIVEDFranzoi MA, Santolaya C, Martin E, Fasse L, Rouby P, Minot-This MS, Di Meglio A, Vaz-Luis I. "Let's talk about risk": co-designing a pathway to assess, communicate and act on individual risk of long-term toxicities after breast cancer. J Cancer Surviv. 2025 Jun 12. doi: 10.1007/s11764-025-01826-0. Online ahead of print. PMID 40504480
- DERIVEDFranzoi MA, Pages A, Papageorgiou L, Di Meglio A, Laparra A, Martin E, Barbier A, Renvoise N, Arvis J, Scotte F, Vaz-Luis I. Evaluating the Implementation of Integrated Proactive Supportive Care Pathways in Oncology: Master Protocol for a Cohort Study. JMIR Res Protoc. 2024 Aug 26;13:e52841. doi: 10.2196/52841. PMID 39186774