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Patient's TeleMonitoring With Amyotrophic Lateral Sclerosis Treated by Non Invasive Ventilation at Home. (TS-VAD)

Primary Purpose

Amyotrophic Lateral Sclerosis, Noninvasive Ventilation

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
teleconsultation
Sponsored by
University Hospital, Toulouse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Amyotrophic Lateral Sclerosis focused on measuring Telemonitoring, amyotrophic lateral sclerosis, noninvasive ventilation, feasibility

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

o inclusion criteria:

  • Patient over 18 years,
  • Patient with Amyotrophic Lateral Sclerosis (ALS),
  • Already fitted by Non Invasive Ventilation (NIV),
  • Patient having signed the informed consent
  • Patient affiliated to a social security scheme,
  • Patient with a correct understanding of the French language,
  • Patient with access to an internet connection at home.

For the caregiver:

  • Adult person
  • Be the patient's primary caregiver
  • Have signed the informed consent intended for the caregiver

    o exclusion criteria:

  • Patient with another cause of chronic respiratory failure: other neuromuscular diseases, Chronic obstructive pulmonary disease (COPD), diffuse interstitial lung disease,
  • Patient under guardianship or under judicial protection,
  • Patient dependent at least 20 hours out of 24 of the non invasive Ventilation (NIV).

Sites / Locations

  • Toulouse University HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

telemonitoring of non invasive ventilation at home

Arm Description

Patients will benefit from a quarterly teleconsultation to assess the study criteria through different questionnaires during 12 months. Ventilation machines make it possible to carry out remote monitoring, with the help of healthcare providers.

Outcomes

Primary Outcome Measures

Patient satisfaction of the telemonitoring of non invasive ventilation at home assessed by CSQ-8 at the end of the study
Consumer satisfaction questionnaire (CSQ-8), minimal score is 8 and maximal score is 32. The best score is 32, that mean that patient is satisfied.

Secondary Outcome Measures

Effect of remote monitoring
evaluated by teleconsultation
Patient satisfaction during the study
assessed by Consumer satisfaction questionnaire (CSQ-8), minimal score is 8 and maximal score is 32. The best score is 32, that mean that patient is satisfied.
Feasibility for caregivers assessed by Zarit questionnaire
Painfulness or burden assessment scale. Minimal score is 0 and maximal score is 76. the higher the score, the greater the difficulty.
Feasibility for caregivers assessed by Depression Anxiety Stress Scales (DASS-21) questionnaire
Painfulness or burden assessment scale. Minimal score is 0 and maximal score is 63. the higher the score, the greater the depression.
Feasibility for nursing staff
data collected through remote monitoring

Full Information

First Posted
February 3, 2021
Last Updated
August 22, 2023
Sponsor
University Hospital, Toulouse
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1. Study Identification

Unique Protocol Identification Number
NCT04797845
Brief Title
Patient's TeleMonitoring With Amyotrophic Lateral Sclerosis Treated by Non Invasive Ventilation at Home.
Acronym
TS-VAD
Official Title
"Patient's TeleMonitoring With Amyotrophic Lateral Sclerosis Treated by Non Invasive Ventilation at Home." Tele Monitoring Ventilation At Home (TM-VAH)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 12, 2021 (Actual)
Primary Completion Date
February 29, 2024 (Anticipated)
Study Completion Date
February 29, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Toulouse

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Single-center, prospective pilot study on patients with amyotrophic lateral sclerosis fitted with noninvasive ventilation. The objective is to assess the satisfaction of remote monitoring of patients on non-invasive ventilation after 12 months.
Detailed Description
The non invasive ventilation is one of treatments used during the amyotrophic lateral sclerosis when patients have a chronic respiratory failure with alveolar hypoventilation signs. It is demonstrated to improve quality of life and prognosis of the disease. These patients, often severely disabled, generally have a negative experience of repeated hospitalizations. Despite everything, medical and paramedical monitoring is necessary, especially when they are fitted with non invasive ventilation (NIV). A quarterly reassessment is recommended . The possibilities of telemonitoring at home have grown considerably in recent years. In addition, the fans are currently able to remotely transfer a certain amount of data to the service provider, making remote monitoring feasible.Our project therefore aims to assess the feasibility of remote monitoring of patients with Amyotrophic Lateral Sclerosis (ALS) fitted with non invasive ventilation (NIV) through the assessment of their satisfaction, using both medical data and data provided by the ventilator. It is a single-center, prospective pilot study on 30 patients with amyotrophic lateral sclerosis fitted with noninvasive ventilation. Patients will benefit from a quarterly teleconsultation to assess the study criteria through questionnaires during 12 months. Ventilation machines make it possible to carry out remote monitoring, with the help of healthcare providers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Amyotrophic Lateral Sclerosis, Noninvasive Ventilation
Keywords
Telemonitoring, amyotrophic lateral sclerosis, noninvasive ventilation, feasibility

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
33 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
telemonitoring of non invasive ventilation at home
Arm Type
Experimental
Arm Description
Patients will benefit from a quarterly teleconsultation to assess the study criteria through different questionnaires during 12 months. Ventilation machines make it possible to carry out remote monitoring, with the help of healthcare providers.
Intervention Type
Other
Intervention Name(s)
teleconsultation
Intervention Description
Patients will benefit from a quarterly teleconsultation to assess the study criteria through different questionnaires during 12 months.
Primary Outcome Measure Information:
Title
Patient satisfaction of the telemonitoring of non invasive ventilation at home assessed by CSQ-8 at the end of the study
Description
Consumer satisfaction questionnaire (CSQ-8), minimal score is 8 and maximal score is 32. The best score is 32, that mean that patient is satisfied.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Effect of remote monitoring
Description
evaluated by teleconsultation
Time Frame
every 3 months during 1 year
Title
Patient satisfaction during the study
Description
assessed by Consumer satisfaction questionnaire (CSQ-8), minimal score is 8 and maximal score is 32. The best score is 32, that mean that patient is satisfied.
Time Frame
every 3 months during 1 year
Title
Feasibility for caregivers assessed by Zarit questionnaire
Description
Painfulness or burden assessment scale. Minimal score is 0 and maximal score is 76. the higher the score, the greater the difficulty.
Time Frame
every 3 months during 1 year
Title
Feasibility for caregivers assessed by Depression Anxiety Stress Scales (DASS-21) questionnaire
Description
Painfulness or burden assessment scale. Minimal score is 0 and maximal score is 63. the higher the score, the greater the depression.
Time Frame
every 3 months during 1 year
Title
Feasibility for nursing staff
Description
data collected through remote monitoring
Time Frame
every 3 months during 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
o inclusion criteria: Patient over 18 years, Patient with Amyotrophic Lateral Sclerosis (ALS), Already fitted by Non Invasive Ventilation (NIV), Patient having signed the informed consent Patient affiliated to a social security scheme, Patient with a correct understanding of the French language, Patient with access to an internet connection at home. For the caregiver: Adult person Be the patient's primary caregiver Have signed the informed consent intended for the caregiver o exclusion criteria: Patient with another cause of chronic respiratory failure: other neuromuscular diseases, Chronic obstructive pulmonary disease (COPD), diffuse interstitial lung disease, Patient under guardianship or under judicial protection, Patient dependent at least 20 hours out of 24 of the non invasive Ventilation (NIV).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sandrine Pontier-Marchandise, MD
Phone
05 67 77 18 46
Email
pontier.s@chu-toulouse.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sandrine Pontier-Marchandise, MD
Organizational Affiliation
University Hopsital Toulouse
Official's Role
Principal Investigator
Facility Information:
Facility Name
Toulouse University Hospital
City
Toulouse
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sandrine Pontier-Marchandise, Dr
Phone
05 67 77 18 46
Email
pontier.s@chu-toulouse.fr

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Patient's TeleMonitoring With Amyotrophic Lateral Sclerosis Treated by Non Invasive Ventilation at Home.

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