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
- Diseases
- ALS (motor neurone disease)
- 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
Sites (2)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU Grenoble Alpes | Grenoble | France | Unknown status |
| CHU Montpellier | Montpellier | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.