Glioma Clinical Trial
Official title:
Randomized Phase II Trial Evaluating Compliance With Monitoring Conducted Either by a Hospital-based Physician in Person or by a Nurse in Remote Monitoring
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).
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 ;
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