Telemonitoring Platform "CUREETY TECHCARE" vs Standard of Care for mTBNC Patients Initiating a First-line Treatment

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This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

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About the trial

The goal of this clinical trial is to assess whether adding telemonitoring (the digital telemonitoring platform "CUREETY TECHCARE"), to standard care, will benefit patients with previously untreated metastatic triple-negative breast cancer starting first-line cancer therapy. The main questions it aims to answer are: * Is patient quality of life improved by using the telemonitoring platform? * Are patients hospitalized less frequently when using the telemonitoring platform? * Is the patient overall survival improved by telemonitoring ? Researchers will compare data from patients using telemonitoring while receiving standard care with data from patients receiving only standard care. Participants using telemonitoring will answer questions about their symptoms on the platform. The platform will analyze these symptoms, assess the patient's general condition and provide advice accordingly. Medical staff will also access the platform to monitor the patient's general condition and contact them if necessary.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • •Podpisana pisemna zgoda na udział w badaniu (może być podpisana przez zaufaną osobę, jeśli pacjent nie jest w stanie tego zrobić)
  • •Wiek 18 lat lub więcej
  • •Rozpoznany potwierdzony biopsją nowotwór piersi z przerzutami typu triple negative (receptory estrogenowe i progesteronowe poniżej 10%, brak receptorów Her2)
  • •Spodziewana długość życia powyżej 6 miesięcy według oceny lekarza
  • •Rozpoczęcie pierwszej linii leczenia systemowego rozpoznanego nowotworu przerzutowego
  • •Dobry stan ogólny (ECOG 0-2)
  • •Dostęp do komputera, tabletu lub smartfona z dostępem do internetu
  • •Zdolność i chęć do wypełniania ankiet przez internet przez cały czas trwania badania

✗ Disqualifies

  • •Uczestnictwo w innym badaniu klinicznym wykorzystującym telemonitorowanie
  • •Niezdolność fizyczna lub psychiczna do używania aplikacji do telemonitorowania, według oceny lekarza
  • •Pozbawienie wolności, areszt ochronny lub poddanie się opiece zastępczej

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
September 29, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (51)

Institut de Cancérologie des Hauts-de-France (ICHF)

Arras, France

Centre Hospitalier d'Auxerre

Auxerre, France

Sainte Catherine - Institut du Cancer Avignon Provence

Avignon, France

CH Aunay-Bayeux

Bayeux, France

Centre Hospitalier Simone Veil de Beauvais

Beauvais, France

ICHF - Centre Pierre Curie

Beuvry, France

Hôpital Simone Veil de Blois

Blois, France

Polyclinique bordeaux nord

Bordeaux, France

Centre Hospitalier Fleyriat

Bourg-en-Bresse, France

Centre de Cancérologie Privé de Caen Maurice Tubiana

Caen, France

Centre Francois Baclesse

Caen, France

Centre hospitalier de Carcasonne

Carcassonne, France

Recherche Oncologie Clinqiue 37 (ROC 37)

Chambray-lès-Tours, France

CH de Cholet

Cholet, France

CH Colmar

Colmar, France

Groupe Hospitalier Public du Sud de l'Oise (GHPSO)

Creil, France

Centre Georges François Leclerc

Dijon, France

Institut Andrée Dutreix

Dunkirk, France

CH Annecy Genevois

Épagny, France

Centre Hospitalier Intercommunal de Fréjus Saint Raphael

Fréjus, France

Groupe Hospitalier Mutualiste de Grenoble

Grenoble, France

CHU de la réunion

La Réunion, France

Clinique Sainte Clotilde

La Réunion, France

Groupe Hospitalier de La Rochelle-Ré-Aunis

La Rochelle, France

CHU Grenoble Alpes

La Tronche, France

Centre Hospitalier Louis Pasteur

Le Coudray, France

Centre Hospitalier Le Mans

Le Mans, France

Centre Hospitalier Emile Roux

Le Puy-en-Velay, France

GHBS Lorient

Lorient, France

Centre Leon Berard

Lyon, France

Clinique de la Sauvegarde

Lyon, France

Hôpital Privé Jean Mermoz

Lyon, France

Institut Paoli Calmettes

Marseille, France

CHI de Mont-de-Marsan et du Pays des Sources

Mont-de-Marsan, France

Centre de Cancérologie du Grand Montpellier

Montpellier, France

Hôpital Privé du Confluent

Nantes, France

Clinique Ambroise-Pare Hartmann

Neuilly-sur-Seine, France

Hôpital Américain de PARIS

Neuilly-sur-Seine, France

CHU de Nimes

Nîmes, France

CHR Orleans

Orléans, France

CHP Sainte-Marie

Osny, France

Diaconesses Croix Saint-Simon Hospital Complex

Paris, France

Centre hospitalier de Pau

Pau, France

CARIO - Hopital Privé des Cotes d'Armor

Plérin, France

CHU de Poitiers

Poitiers, France

Institut Godinot

Reims, France

Clinique Mathilde - Les Hôpitaux Privés Rouennais

Rouen, France

CHU de Saint-Etienne

Saint-Etienne, France

Hia Begin

Saint-Mandé, France

CHU de Tours

Tours, France

Institut de Cancérologie de Lorraine

Vandœuvre-lès-Nancy, France

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/1/2026.

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