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NCT05621213Terminated

Satisfaction of Patients With Amyotrophic Lateral Sclerosis Regarding Home Assisted Teleconsultation

Satisfaction of Patients With Amyotrophic Lateral Sclerosis Under Non-invasive Ventilation Regarding Home Assisted Teleconsultation

Source: ClinicalTrials.gov · Last updated 6 Feb 2026

Brief summary (registry, in English)

Satisfaction of patients with amyotrophic lateral sclerosis under non-invasive ventilation regarding home assisted teleconsultation

Status (registry)
Terminated
Study type
Interventional
Enrollment
38 (actual)
First submitted
27 Oct 2022
Start date
13 Jan 2023
Primary completion date
31 Dec 2024
Lead sponsor
AGIR à Dom
NCT number
NCT05621213

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patient currently participating or having participated in the month prior to inclusion in another clinical interventional research study that may have an impact on the study, this impact is left to the discretion of the investigator

Age

  • Pregnant women (for women of childbearing age and in the absence of reliable contraception, the β-HCG (human chorionic gonadotropin) assay will be performed), parturient women, breastfeeding women,

Other

  • Patient not available or wishing to change region within 3 months of inclusion
  • Persons referred to in articles L1121-5 to L1121-8 of the French Public Health Code (corresponding to all protected persons)
  • persons deprived of their liberty by judicial or administrative decision,
  • persons under legal protection

Who the study is looking for

  • Patient with a diagnosis of ALS coming for a follow-up consultation with their pneumologist
  • Daily NIV compliance of more than 4 hours in the month prior to inclusion
  • Living at home
  • Patient with a natural caregiver
  • Patient equipped with computer equipment adapted for teleconsultation (tablet, computer, telephone... with an internet connection)
  • Patient able to read and understand the procedure, and able to express consent for the study protocol
  • Patient, or his or her caregiver, able to sign the consent to participate by himself or herself

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
CHU Grenoble AlpesGrenobleFranceUnknown status
CHU MontpellierMontpellierFranceUnknown status

Are you the coordinator? Confirm the details

This page is information, not medical advice. Discuss any trial with your doctor.