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Spots Global Cancer Trial Database for Impact of a Process Optimizing the Decision to Continue or Stop Cancer Treatments in Patients With Advanced Non-small Cell Lung Cancer.

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Trial Identification

Brief Title: Impact of a Process Optimizing the Decision to Continue or Stop Cancer Treatments in Patients With Advanced Non-small Cell Lung Cancer.

Official Title: Impact of a Process Optimizing the Decision to Continue or Stop Cancer Treatments in Patients With Advanced Non-small Cell Lung Cancer.

Study ID: NCT04823377

Study Description

Brief Summary: Sequential comparative prospective interventional study evaluating the impact of the use of an optimization device of the decision of cancer treatment on aggressiveness of end of life care. Comparison between a first period, period (A), of care as usual and a second period, period (B), of systematic and iterative use of a device for optimizing the decision to continue an anti-cancer treatment.

Detailed Description: We propose to study the optimization of this decision process in an advanced Non-Small-Cell Lung Carcinoma (NSCLC) population, with a Performance Status (PS) ≥ 2 (median survival of approximately 3 months) piloting iteratively (before each decision to continue treatment) a process consisting of an evaluation framework (30 items to be answered by the oncologist with the patient), consolidating: 1. clinical parameters; 2. doctors' expectations regarding the continuation of anticancer treatment; 3. patient expectations and preferences; 4. the possibility of referring the patient to a supportive care specialist and strengthening home care. The process triggers a dialogue between the patient and the oncologist, based on facts and seeks objectivity, ultimately allowing a shared decision. In this prospective comparative study, the rate of systemic oncological treatment during the last month of life will be measured consecutively, over a period of usual management, followed by a period of systematic application of a process of optimization of the medical decision.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

CH Abbeville, Abbeville, , France

CH du Pays d'Aix, Aix-en-Provence, , France

CHU Amiens - Hôpital Sud, Amiens, , France

CHU Angers, Angers, , France

CHR Metz-Thionville - Hôpital de Mercy, Ars-Laquenexy, , France

CH Henri Duffaut Avignon, Avignon, , France

Institut Sainte-Catherine, Avignon, , France

AP-HP Ambroise Paré, Boulogne-Billancourt, , France

CHI de Compiègne-Noyon, Compiègne, , France

CHU Sud Francilien, Corbeil-Essonnes, , France

Clinique des Cèdres, Cornebarrieu, , France

CH Intercommunal de Créteil, Créteil, , France

CGFL, Dijon, , France

CHU Grenoble Alpes, Grenoble, , France

CHD Vendée, La Roche-sur-Yon, , France

CHRU Lille, Lille, , France

Centre Léon Bérard, Lyon, , France

Institut Curie, Paris, , France

AP-HP Cochin, Paris, , France

AP-HP Bichat, Paris, , France

AP-HP Tenon, Paris, , France

Institut Curie, Saint-Cloud, , France

CH Saint-Malo, Saint-Malo, , France

Hôpital Foch, Suresnes, , France

Clinique Tessier, Valenciennes, , France

Contact Details

Name: Marie-Ange MASSIANI, MD

Affiliation: Institut Curie

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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