Informations générales (source: ClinicalTrials.gov)
Digital Monitoring With Patient-Reported Outcomes in Cancer Care: A Randomized Controlled Trial RC - 102 (Resilience Care - 102)
Interventional
Phase 3
Resilience (Voir sur ClinicalTrials)
avril 2025
décembre 2029
08 septembre 2025
The goal of this clinical trial is to learn if Resilience PRO, a digital solution
performing remote symptoms monitoring, can improve the quality of life of patients with a
diagnosis of cancer receiving systemic anticancer treatment.
The main question it aims to answer is:
- Do patients with a diagnosis of cancer receiving systemic anticancer therapy and
using Resilience PRO have an improved quality of life? Researchers will compare
patients using Resilience PRO plus care as usual to patients receiving care as usual
only.
Participants in the intervention arm will use Resilience PRO, a mobile phone application
regularly asking participants about their symptoms. For clinically important symptoms, an
alert is sent to the care team that can incorporate that information to timely adjust the
care of the participants. Participants both in the control arm and in the intervention
arm will further receive care as usual.
Etablissements
| Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| CLCC INSTITUT GUSTAVE ROUSSY | Sabrina Ikene | Contact (sur clinicalTrials) | |||
| Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
| AP-HM Assistance Publique - Hôpitaux de Marseille Hôpital de la Timone - 13005 - Marseille - France | Nathalie Moureau | Contact (sur clinicalTrials) | |||
| AP-HP Hôpitaux Universitaires La Pitié Salpêtrière - 75013 - Paris - France | Direction de la Recherche Clinique et de l'Innovation | Contact (sur clinicalTrials) | |||
| Centre Clinical Elsan - 16800 - Soyaux - France | Corine Bustreau | Contact (sur clinicalTrials) | |||
| Centre de Cancérologie Les Dentellières - 59300 - Valenciennes - France | Stéphanie Vermoesen | Contact (sur clinicalTrials) | |||
| Centre Hospitalier de la Côte Basque - 64100 - Bayonne - France | Emmanuelle Vignes | Contact (sur clinicalTrials) | |||
| Centre Hospitalier du Pays d'Aix - Centre Hospitalier Intercommunal Aix-Pertuis - 13100 - Aix-en-Provence - France | Nabila Akkache | Contact (sur clinicalTrials) | |||
| Centre Hospitalier Henri Mondor-Aurillac - 15000 - Aurillac - France | Manon MONCET | Contact (sur clinicalTrials) | |||
| Centre Hospitalier Intercommunal Toulon - La Seyne sur Mer - 83056 - Toulon - France | Charline Genin | Contact (sur clinicalTrials) | |||
| Centre Hospitalier Universitaire de Caen Normandie - 14033 - Caen - France | Justine Lecache | Contact (sur clinicalTrials) | |||
| Centre Hospitalier Universitaire de Clermont-Ferrand - 63003 - Clermont-Ferrand - France | Céline Bonhomme | Contact (sur clinicalTrials) | |||
| Centre Hospitalier Universitaire de Lille - 59037 - Lille - France | Jeremy DRUGEON | Contact (sur clinicalTrials) | |||
| Centre Hospitalier Universitaire de Nantes - 44093 - Nantes - France | Celine LEREBOURG | Contact (sur clinicalTrials) | |||
| Centre Hospitalier Universitaire de Nice - 06000 - Nice - France | Enora Valle | Contact (sur clinicalTrials) | |||
| Centre Hospitalier Universitaire de Nîmes - 30029 - Nîmes - France | Shanice Roriz | Contact (sur clinicalTrials) | |||
| Centre Hospitalier Universitaire Grenoble - Alpes - 38700 - La Tronche - France | Amandine Ramond | Contact (sur clinicalTrials) | |||
| Centre Hospitalier Universitaire Sud Réunion - 97448 - Saint-Pierre - France | Sara MIKOLASEK | Contact (sur clinicalTrials) | |||
| Clinique Mutualiste Bretagne Occidentale - 29000 - Quimper - France | Karine Mas | Contact (sur clinicalTrials) | |||
| Clinique Mutualiste de l'Estuaire - 44606 - Saint-Nazaire - France | Enora Valle | Contact (sur clinicalTrials) | |||
| Clinique Pasteur - 31076 - Toulouse - France | Sophie Bringer | Contact (sur clinicalTrials) | |||
| Clinique Teissier - 59300 - Valenciennes - France | Marielle Fery | Contact (sur clinicalTrials) | |||
| GHICL Hôpital Saint Vincent de Paul - 59000 - Lille - France | Catherine CUNISSE | Contact (sur clinicalTrials) | |||
| Hôpital Privé de la Loire (HPL) - Saint Etienne - 42100 - Saint-Étienne - France | Sandy MESSAOUDENE | Contact (sur clinicalTrials) | |||
| Hôpital Privé de Provence - 13080 - Aix-en-Provence - France | Salima DELLYS | Contact (sur clinicalTrials) | |||
| Hôpital Privé du Confluent - 44200 - Nantes - France | Emma CADET | Contact (sur clinicalTrials) | |||
| Hôpital Privé Jean Mermoz - Institut de Cancérologie - 69008 - Lyon - France | Gaëlle Le Guludec | Contact (sur clinicalTrials) | |||
Critères
Tous
Inclusion Criteria:
- Age: Adults ≥ 18 years.
- Informed Consent: Patient giving signed informed consent to participate in the RC -
102 clinical study.
- Diagnosis: Patients with cancer at any stage.
- Systemic Treatment
- Remote Monitoring Eligibility: Access to a smartphone
- Language: Ability to understand and communicate in the language(s) in which the
trial is conducted.
- Age: Adults ≥ 18 years.
- Informed Consent: Patient giving signed informed consent to participate in the RC -
102 clinical study.
- Diagnosis: Patients with cancer at any stage.
- Systemic Treatment
- Remote Monitoring Eligibility: Access to a smartphone
- Language: Ability to understand and communicate in the language(s) in which the
trial is conducted.
- Age: Patients under 18 years of age.
- Life Expectancy: Patients with a life expectancy of less than 6 months as estimated
by the treating physician.
- Concurrent remote monitoring
- HSCT or CAR-T Therapy
- Cognitive Impairment
- Pregnancy or breastfeeding
- Subject under administrative or judicial control