Real Life Study Evaluating the Clinical and Organisational Impact of Moovcare® Lung Connected Medical Device in Lung Cancer Patients : REAL-MOOV-LUNG

Last updated: March 11, 2025
Sponsor: Institut Curie
Overall Status: Completed

Phase

N/A

Condition

Non-small Cell Lung Cancer

Cancer

Lung Disease

Treatment

Patients treated for their lung cancer.

Clinical Study ID

NCT04934865
IC 2020-13
  • Ages > 18
  • All Genders

Study Summary

Evaluation of patient's proportion, whose management care has been modified at least once and specially by Moovcare® Lung application at 12 and 24 months.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Patient with lung cancer at any diagnostic stage and histology.

  2. Patient willing to use the follow-up setting with Moovcare® Lung apps.

  3. Age ≥ 18 years.

  4. Patient received anti-cancer treatment (surgery, chemotherapy, radiation (stereotaxyor not) or radio-chemotherapy association ended less than 12 weeks (Cohort 1post-treatment); or during maintenance treatment or consolidation by chemotherapy ortargeted therapy, or by immunotherapy initiated less than 12 weeks (Cohort 2 duringtreatment).

  5. Imaging tumor evaluation less than 12 weeks showing disease control (response orstability according to RECIST 1.1 criteria).

  6. Patient with symptomatic score on Moovcare® Lung apps less than 7.

  7. Patient (or relatives) with internet access, a personnal e-mail box and asmartphone.

  8. Patient with social security affiliation.

  9. Signed informed consent form.

Exclusion

Exclusion Criteria:

  1. Patient with progression after the first evaluation of initial treatment.

  2. Pregnancy and breast-feeding.

  3. Patient under tutorship or guardianship.

  4. Dementia, mental alteration or psychiatric pathology influencing patient consentprocedure and/or protocol observance and study follow-up.

  5. Patient enable to protocol follow-up for psychological, social, familial orgeographical reasons.

Study Design

Total Participants: 240
Treatment Group(s): 1
Primary Treatment: Patients treated for their lung cancer.
Phase:
Study Start date:
October 07, 2021
Estimated Completion Date:
February 28, 2025

Study Description

Primary objective of the study:

The primary objective is a clinical one and is to evaluate the proportion of patients, whose management care has been modified at least once and specially by Moovcare® Lung application at 12 and 24 months.

Connect with a study center

  • Ico Angers

    Angers, 44805
    France

    Site Not Available

  • Chu Argenteuil

    Argenteuil, 95100
    France

    Site Not Available

  • Centre Hospitalier Public du Cotentin

    Cherbourg, 50100
    France

    Site Not Available

  • Hôpital Forcilles

    Férolles Attilly, 77150
    France

    Site Not Available

  • Hôpital Nord-Ouest

    Gleize, 69400
    France

    Site Not Available

  • Hopital Franco Britannique

    Levallois-Perret, 92300
    France

    Site Not Available

  • Centre Oscar Lambret

    Lille, 59000
    France

    Site Not Available

  • Polyclinique de Limoges - Site de François CHENIEUX

    Limoges, 87039
    France

    Site Not Available

  • AP-HM La Timone

    Marseille, 13915
    France

    Site Not Available

  • Clinique Saint-George

    Nice, 06100
    France

    Site Not Available

  • CHU de PAU

    PAU, 64046
    France

    Site Not Available

  • Institut Curie

    Paris, 75005
    France

    Site Not Available

  • CH Annecy Genevois

    Pringy, 74374
    France

    Site Not Available

  • Clinique mutualiste de l'ESTUAIRE

    Saint Nazaire, 44600
    France

    Site Not Available

  • Institut Curie

    Saint-cloud, 92210
    France

    Site Not Available

  • Nouvel Hôpital Civil

    Strasbourg, 67091
    France

    Site Not Available

  • Hopital Robert Schumann

    Vantoux, 57070
    France

    Site Not Available

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