Development and Validation of a Tool for Patient-reported Assessment of Cancer-related Financial Toxicity in Italy

NCT03473379 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 440

Last updated 2023-03-24

No results posted yet for this study

Summary

The aim of this study is to develop and validate a patient-reported-outcome instrument (PROFTC-I: Patient Reported Outcome Financial Toxicity in Cancer - Italy) able to describe and measure financial problems of Italian patients receiving cancer treatment.

Conditions

Sponsors & Collaborators

  • National Cancer Institute, Naples

    lead OTHER

Principal Investigators

  • Francesco Perrone · Istituto Nazionale Tumori IRCCS - Fondazione G. Pascale

  • Jane Bryce · Istituto Nazionale Tumori IRCCS - Fondazione G. Pascale

  • Ciro Gallo · University of Campania Luigi Vanvitelli

  • Silvia Riva · St. Mary University, Twickenham, London, GB

  • Fabio Efficace · Northwestern University, Feinberg School of Medicine, GIMEMA,EORTC Quality of Life Group - Rappresentante GIMEMA

  • Francesco De Lorenzo · AIMAC and European Cancer Patient Coalition

  • Elisabetta Iannelli · Segretario Generale FAVO

  • Laura Del Campo · FAVO

  • Francesca Traclò · AIMAC

  • Massimo Di Maio · AO Ordine Mauriziano

  • Luciano Frontini · Federation of Italian Cooperative Oncology Groups

  • Vincenzo Montesarchio · Oncologia, Azienda dei Colli, Napoli - CIPOMO

  • Lara Gitto · Centro per gli Studi Economici e Internazionali - Economic Evaluation & Health Technology Assessment (CEIS EEHTA), Università di Roma "Tor Vergata"

  • Claudio Jommi · Dipartimento di Scienze del Farmaco, Università del Piemonte Orientale; Osservatorio Farmaci, Cergas, SDA Bocconi

  • Concetta Maria Vaccaro · Welfare e Salute CENSIS (Centro Studi Investimenti Sociali), Roma

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-03-01
Primary Completion
2024-02-01
Completion
2024-07-01

Countries

  • Italy

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03473379 on ClinicalTrials.gov