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Clinical Trial Summary

This is a multicenter, interventional, randomized study among adult patients recently diagnosed with a rare tumor (<12 months). The study will aim to compare compliance with the personalized post-treatment surveillance plan, established for each patient according to national guidelines, when the surveillance is conducted in person by a hospital-based physician (control arm) or remotely by a trained nurse (experimental arm).


Clinical Trial Description

The primary objective of this study is to compare 2-year compliance with the personalized post-treatment surveillance plan between the two arms. The secondary objectives are to compare between the two arms : - Long-term compliance (5-year follow-up) - Use of care - Oncological events and their management - Supportive care needs The exploratory objectives are to : - Evaluate the costs in terms of medical transportation - Evaluate and compare patients' satisfaction and psychological well-being (in terms of anxiety/depression) - Evaluate the homogeneity of the impact of the intervention according to covariates (gender, tumor pathology, occupational status, and center) - Evaluate the reasons for recruitment failures ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05500391
Study type Interventional
Source Centre Oscar Lambret
Contact Laurence ROTSAERT
Phone 0320295860 / 0320295918
Email l-rotsaert@o-lambret.fr
Status Recruiting
Phase Phase 2
Start date February 28, 2024
Completion date October 2029

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